Congenital obstructive nephropathy is a major cause of chronic kidney disease (CKD) in children. The contribution of changes in the identity of renal cells to the pathology of obstructive nephropathy is poorly understood. Using a partial unilateral ureteral obstruction (pUUO) model in genetically modified neonatal mice, we traced the fate of cells derived from the renal stroma, cap mesenchyme, ureteric bud (UB) epithelium, and podocytes using Foxd1Cre, Six2Cre, HoxB7Cre, and Podocyte.Cre mice respectively, crossed with double fluorescent reporter (membrane-targetted tandem dimer Tomato (mT)/membrane-targetted GFP (mG)) mice. Persistent obstruction leads to a significant loss of tubular epithelium, rarefaction of the renal vasculature, and decreased renal blood flow (RBF). In addition, Forkhead Box D1 (Foxd1)-derived pericytes significantly expanded in the interstitial space, acquiring a myofibroblast phenotype. Degeneration of Sine Oculis Homeobox Homolog 2 (Six2) and HoxB7-derived cells resulted in significant loss of glomeruli, nephron tubules, and collecting ducts. Surgical release of obstruction resulted in striking regeneration of tubules, arterioles, interstitium accompanied by an increase in blood flow to the level of sham animals. Contralateral kidneys with remarkable compensatory response to kidney injury showed an increase in density of arteriolar branches. Deciphering the mechanisms involved in kidney repair and regeneration post relief of obstruction has potential therapeutic implications for infants and children and the growing number of adults suffering from CKD.
Obstructive nephropathy, the leading cause of chronic kidney disease (CKD) in children, begins during embryonic and fetal development of the urinary tract [1–3]. Prolonged obstruction along the urinary tract results in marked morphological and pathological changes in the developing kidney, affecting its normal development and function. Pediatric patients with congenital obstructive nephropathy generally require surgical intervention and careful post-surgical management to minimize renal injury. Indications and timing for surgical intervention are highly controversial, and the procedure may still fail to prevent progressive loss of renal function even when surgical release is performed in utero. There is therefore an urgent need to understand the cellular and molecular mechanisms involved in kidney repair and develop new treatments to avoid end-stage renal diseases in these infants and children.
To simulate human congenital urinary tract obstruction in utero, animal models of reversible variable partial unilateral ureteral obstruction (pUUO) have been developed [4–9]. In humans, nephrogenesis is completed prior to full-term birth , but in rats and mice most nephrons are formed during the first week of post-natal life [11–13]. Mid gestation obstructive nephropathy in the human fetus is modeled by pUUO in the newborn mouse, in which relief of obstruction at 7 days results in improvement of renal architecture and function . This model was therefore chosen to explore the mechanisms promoting kidney repair and regeneration. Significant remodeling of kidney architecture following the release of obstruction is likely to involve changes in cell fate. Therefore, using genetic labeling we investigated the morphological and cell fate changes that occur in the vascular, tubular, and interstitial compartments during neonatal pUUO and after its release in mice.
Mice and animal surgery
To trace the lineage of stromal, cap mesenchyme, podocyte, and ureteric bud (UB) derived cells, we crossed Forkhead Box D1 (Foxd1)-GFP-Cre (Foxd1Cre ); Sine Oculis Homeobox Homolog 2 (Six2)- Tet-off-eGFPCre (TGC)tg (Six2Cre ); PodocyteCre (generated in our lab, full details of its generation and characterization will be documented elsewhere [R.A.G. and M.L.S.S.-L. unpublished data]) and Hoxb7Cre  respectively, with double fluorescent membrane-targetted tandem dimer Tomato (mT)/membrane-targetted GFP (mG) Cre reporter mice . Pups derived from these crosses were subjected to pUUO (n=170) or sham operation (n=76) at 24–48 h following birth (Figure 1A). Partial obstruction was created by means of a ligature tied around the ureter apposed to a 3-4 mm length of 0.2-mm thickness stainless steel wire and the wire was removed after ligation. A second surgery was performed at 1 week after obstruction (WO) only for some animals to release the obstruction . Tissues were collected at 1, 3, and 8 WO or at 1, 2, and 7 weeks after release (WR). A second surgery was performed at one WO only for some animals (n=75) to release the knot created around the ureter and the obstruction was maintained for the rest of them. India Ink was injected into the kidneys to check for ureteral patency. We scored the kidneys at the time of harvest according to the degree of hydronephrosis to evaluate the extent of damage due to obstruction and the reduction in hydronephrosis post-release. The scoring was in the scale of hydronephrosis index 1–4 (Figure 1C): 1- Kidneys normal in appearance; 2- Kidneys appear hydronephrotic (i.e. distended), but without obvious translucent areas; 3- Kidneys are distended with obvious translucent areas, but retain significant remaining parenchyma; 4- Very severe hydronephrosis with little if any remaining parenchyma . Morphometric analyses were done by measuring the body weight of the sham and surgery animals at 0, 1, 2, 3, and 8 weeks and kidney weight at the time of tissue collection at 1, 3, and 8 WO; 1, 2, and 7 WR.
Release of obstruction significantly resolves the renal damage due to obstruction
All procedures were performed in accordance to the Guidelines for the Care and Use of Laboratory Animals published by the United States National Institutes of Health (https://grants.nih.gov/grants/olaw/guide-for-the-care-and-use-of-laboratory-animals.pdf) and were approved by the University of Virginia Animal Care and Use Committee.
Histology and immunostaining
Animals were anesthetized with tribromoethanol at 1, 3, and 8 WO and 1, 2, and 7 WR. Kidneys were removed, weighed, and either fixed in 2% paraformaldehyde (PFA) for 1 h at 4°C for frozen sections or in Bouin’s fixative overnight for paraffin sections. Sections (5–10 µm) from paraffin embedded or cryo-fixed tissues were used for histological analysis. Bouin’s fixed paraffin kidney sections from 1-week-old animals were stained with Hematoxylin and Eosin to analyze the vascular structures. Fibrotic damage was checked using Masson’s trichrome staining . Oil Red staining was used to assess lipid accumulation . Immunostaining was performed as previously described  using the following antibodies with a minimum of three replicates in each of the treatment groups (Sham, pUUO, and pUUO+Release): anti-α-smooth muscle actin (α-SMA) (1:10000, mouse monoclonal isotype Ig2a; catalog number: A2547, Sigma, St. Louis, MO), to detect cells expressing α-SMA including myofibroblasts, anti-PDGFRβ (platelet-derived growth factor receptor β-1:100, Rabbit monoclonal, catalog number: 3169, Cell Signaling Technology) to identify the interstitial pericytes. Kidney sections were stained with biotinylated Lotus tetragonolobus lectin (1:50, catalog number: B1325, Vector Laboratories, Burlingame, CA, U.S.A.) for identification of proximal tubules and Lc3BII to detect autophagy in the tubular epithelium (1:200, Rabbit polyclonal, catalog number: 2775, Cell Signaling Technology). Anti-platelet endothelial cell adhesion molecule-1 (PECAM) (1:1000, Rabbit Polyclonal, catalog number: sc-1506-R, Santa Cruz Biotechnology) was used to label endothelial cells, anti-Laminin (1:500, Rabbit polyclonal, catalog number: L9393, Sigma), and anti-acetylated α tubulin (1:10000, mouse monoclonal, catalog number: T6793, Sigma) to analyze the primary cilia status in the tubular epithelium, anti-HO1 (1:400, Rabbit, Polyclonal, catalog number: SPA-896, EnzoLife Sciences), anti-4 Hydroxynonenal (1:300, Rabbit polyclonal, catalog number: ab46545, Abcam), anti-hypoxia-inducible factor 1-α (Hif1α) (1:600, Rabbit polyclonal, catalog number: GTX127309, GeneTex) and anti-hypoxia-inducible factor 2-α (Hif2α) (1:800, Mouse monoclonal, catalog number: GTX30123, GeneTex) to assess renal oxidative stress and hypoxia, anti p-histone H3 (1:200, Rabbit polyclonal, catalog number: 9701, Cell Signaling Technology) to identify mitotic cells, anti-Nanog homeobox (Nanog) (1:100, Rabbit polyclonal, catalog number: ab84447, Abcam), and anti-Oct-4 (1:250, Rabbit polyclonal, catalog number: ab19857, Abcam) (embryonic stem cell markers) to detect the potential of de-differentiation in the process of tissue repair post-obstruction. For immunofluorescence, secondary antibodies Alexa Fluor 350 Goat anti-mouse IgG (H+L) (α-SMA), Alexa Fluor 568 Donkey anti-mouse IgG (H+L) (acetylated α-tubulin), Alexa Fluor 488 Donkey anti-rabbit (Laminin), Alexa Fluor 350 Goat anti-rabbit (1:500), streptavidin–conjugated Alexa Fluor 350 (lotus lectin-1:500 dilution; Life Technologies, Carlsbad, CA) were used. Immunostaining using DAB was performed with the appropriate Vectastain ABC kits (Vector Laboratories, Burlingame, CA).
Quantitation of renal progenitor cells and their progeny in kidney damage and repair
Imaging of GFP+ cells on kidneys from various tissue-specific Cre lines was done using a Leica DFC310 FX digital camera connected to a Leica DFC 480 microscope and quantitation of GFP positive interstitial and collecting duct areas using ImageJ software (National Institutes of Health).
Measurement of the GFP+ positive interstitial and collecting duct areas
Kidney sections from Foxd1Cre; mTmG mice were imaged for quantitating changes in the GFP+ interstitial cells. To measure only the expanded GFP+ interstitial cells, the additional GFP+ structures in the image such as glomeruli and major arteries were removed for quantitation. The GFP+ interstitial area was normalized for the total kidney area of each image and expressed as percent area fraction:
Kidney sections from HoxB7Cre;mTmG mice were imaged as described above to measure the GFP+ collecting duct area. The measured collecting duct area was normalized for the total kidney area of the micrographs and expressed as percentage:
Atubular glomeruli counts
Counting of atubular glomeruli was performed as previously described [22,23]. Severe kidney injury during pUUO in neonatal mice results in the formation of atubular glomeruli due to the loss of tubular cells in the glomerulo–tubular junction. Extensive work done through serial sectioning analyses has proved that release of obstruction prevents the tubular degeneration and thus ameliorates the formation of atubular glomeruli [22,23]. In the current study, we adopted an indirect method of quantitating the atubular glomeruli in lotus lectin-stained images of kidney sections derived from Six2Cre;mTmG mice. Glomeruli showing absence of lectin positive cells at the neck of the glomeruli connecting to proximal tubules were designated as atubular. Atubular glomeruli counts were further normalized for the kidney area measured for each image.
Quantitation of fibrotic area and PDGFRβ positive area
Quantitations of collagen-positive area with Masson’s trichrome staining and PDGFRβ staining were done using ImageJ software. The quantitated area was normalized for the total kidney area of the micrographs and expressed as percentage.
RNA extraction and PCR analysis
Kidneys were dissected and preserved in RNA later (Life Technologies, Grand Island, NY). Tissues were homogenized with TRIzol reagent (Life Technologies). RNA was isolated from the tissue homogenate by phase separation using BCP (Molecular Research Centre, Cincinnati, OH). The isolated RNA was further purified using RNeasy mini-spin column (Qiagen, Valencia, CA). cDNA was prepared using Moloneymurine leukemia virus reverse transcriptase and an oligo(dT)15 primer (Promega) following the manufacturer’s protocol. Quantitative PCR was performed in a CFXConnect system (Bio-Rad, Hercules, CA) using SYBR Green I (Invitrogen Molecular Probes) and Taq DNA polymerase (Promega), following the manufacturer’s instructions. mRNA values were normalized to Rps14 (Ribosomal Protein S14) expression. The changes in expression were determined by the ΔΔCt (cycle threshold) method . The primers used for quantitative reverse-transcription PCR (qRT-PCRs) are listed in Table 1.
|Target gene .||Forward primer (5′–3′) .||Reverse primer (5′–3′) .|
|Target gene .||Forward primer (5′–3′) .||Reverse primer (5′–3′) .|
Abbreviations: Acox1, acyl-coenzyme A oxidase 1, palmitoyl; Acox2, acyl-coenzyme A oxidase 2, branched chain; Cox4, cytochrome c oxidase subunit 4I1; Cpt1a, carnitine palmitoyltransferase 1a, liver; Cpt2, carnitine palmitoyltransferase 2; Hoxb7, homeobox B7; Mafb, v-maf musculoaponeurotic fibrosarcoma oncogene family, protein B; Nrf1, nuclear respiratory factor 1; Nrf2, nuclear factor, erythroid derived 2, like 2; PPARα1, peroxisome proliferator activated receptor α; Tfam, Transcription factor A, mitochondrial.
In order to evaluate the changes in fourth and fifth order arterial branching during injury and repair, we performed arterial micro-dissections as it provides details on higher order branches of the arterial tree. This procedure of micro-dissection (using HCl-macerated kidneys) preserves spatial geometry of the whole renal arterial tree without a loss in arterioles. Arterial micro-dissections were done on kidneys harvested from 1 and 8 weeks old animals. Briefly the kidneys attached to the aorta were incubated in 6 M hydrochloric acid for an hour, washed several times with acidified water (pH 2.5). The entire arterial trees were carefully dissected under direct stereoscopic visualization and imaged for counting the arterial branches  in kidneys from sham, obstructed, and released groups of animals.
Renal blood flow measurement
Renal blood flow (RBF) was assessed in the obstructed and post-released kidneys and compared with sham-operated kidneys using contrast-enhanced ultrasonography and steady-pulsed arterial spin labeling (spASL) MRI techniques at the University of Virginia molecular imaging core facilities.
In 3-week-old obstructed and released animals RBF measurements were performed using the contrast-enhanced ultrasonography technique as previously described . Mice were anesthetized with 2% isoflurane in air. The fur was removed by shaving and a depilatory cream. Mice were then positioned on a three-coordinate stage with the heating pad maintained at 37°C. Pre-warmed ultrasound (US) gel was placed on the depilated skin for imaging using a Siemens Acuson c512 imaging system, equipped with a 15L8w transducer. The kidney was localized in real-time using conventional B-mode imaging with a frequency of C10 MHz. Once the kidney was identified, the contrast function was initiated in Cadence CPS mode with a frequency of P10MHz; BMI-1.9 and IMI-0.21. A 20-µl intravenous bolus injection of the microbubble contrast agent (∼1 billion microbubbles per ml; mean bubble size ∼2 µm) was then administered via retro-orbital plexus. Once a steady-state was obtained and no evidence of acoustic shadowing was present, 15-s videos of microbubble destruction and replenishment were recorded. Microbubbles were destroyed using the BURST function and were of 3 s in duration. After a minimum of three videos were recorded for each animal, the length and width of the kidneys were measured using the CALIBER application. For data acquisition, the resultant images were analyzed using the Sequoia analysis software (SYNGO) following the protocol as described previously .
Perfusion measurements in 6-week-old animals were done using a spASL-MRI technique as described previously . Briefly, MRI scans were performed using a 7T Clinscan system (Bruker, Ettlingen, Germany) with a 30-mm diameter birdcage radio frequency coil. The electrocardiogram (ECG), body temperature, and respiration were monitored during imaging (SA Instruments, Stony Brook, NY). During MRI, mice were anesthetized with 1.25% isoflurane and maintained at 36 ± 0.5°C using circulating warm water. After localizer imaging, spASL-MRI  was performed on a mid-renal long-axis slice. As shown in Figure 5B, spASL uses an arterial blood tagging scheme consisting of a regional inversion pulse over the incoming renal artery. The corresponding control scheme uses an inversion pulse applied symmetrically from the imaging plane. Parameters for spASL included: FOV = 38 × 38 mm2, matrix size = 128 × 128, TR = 10 ms, TE = 2.5 ms, flip angle = 7°, slice thickness = 1 mm, saturation band thickness = 10 mm, number of averages = 9, and scan time ∼6 min. RBF was quantitated using previously described methods .
Confocal and scanning TEM imaging
Primary cilia status in the tubular epithelium was assessed using a confocal microscope (Olympus Fluo View 1000). For scanning TEM (STEM) analyses, 1- and 3-weeks-old animals of sham and surgery groups were fixed by cardiac perfusion through left ventricle with 4% PFA and 2% glutaraldehyde in cacodylate buffer. Tissues were harvested and analyzed using the Advanced Microscopy Facility at the University of Virginia. Semi-thin sections of 0.5 µm thickness were cut and stained with Toluidine Blue and imaged using light microscopy.
Data were analyzed using GraphPad Prism 7.04. Results are expressed as mean ± S.E.M. Comparisons between more than two groups were made by one-way ANOVA for normally distributed data and by Kruskal–Wallis one-way ANOVA for data not normally distributed. For comparisons between two groups, a two-tailed Student’s t test was applied for normally distributed data and Mann–Whitney U-test for data not normally distributed. A P-value ≤0.05 was considered as significant.
Release of obstruction reduces hydronephrosis resulting from persistent obstruction
The general experimental design for surgeries and tissue collection is shown in Figure 1A. Severe hydronephrosis after 1 WO resulted in loss of renal medulla and formation of fluid filled kidneys (Figure 1B). Following 8 weeks of pUUO, ipsilateral kidneys underwent atrophy, whereas contralateral kidneys underwent compensatory growth (Figure 1B). Release of obstruction at 7 days, resulted in marked reduction in hydronephrosis, and improvement of kidney’s gross morphology (Figure 1B). Given that the degree of hydronephrosis varies amongst animals, to make comparisons during and after obstruction, we generated a hydronephrosis index (severity score 1–4, ) (Figure 1C). Notably in 3-week-old animals, 36% of kidneys with severe damage (index 3–4) recovered to index 1 whereas 96% of kidneys with hydronephrosis index 2 recovered to index 1. After 1 WO, body weight was decreased in all animals (males and females), but with increasing age, body weight was no longer different between groups indicating that the surgical procedure did not affect the somatic growth of the animals in either sex (Supplementary Figure S1A). The weight of the contralateral (right) kidneys of obstructed animals increased significantly compared with contralateral kidneys of shams, consistent with compensatory growth of the right kidneys (Supplementary Figure S1B). However, relief of obstruction prevents a further increase in the growth of the contralateral kidneys, as the kidney to body weight ratio of contralateral kidneys following the relief of obstruction was not significantly different compared with contralateral kidneys of shams (Supplementary Figure S1B). The severity of hydronephrosis and recovery capacity following the release of obstruction did not differ between males and females (Supplementary Figure S1C,D).
Release of obstruction promotes regeneration of the renal vasculature
As the vasculature plays a pivotal role in development and maintenance of the kidney architecture, we examined the changes in the renal vasculature during kidney injury and repair.
Micro-dissection of the renal arterial trees at 1 WO showed a decrease in arteriolar branching in the obstructed kidneys (Supplementary Figure S2). With the persistence of the obstruction, the renal arterial trees at 8 weeks revealed extensive damage and stunting of the vasculature characterized by impaired arterial branching and significant arteriolar loss (Figure 2A,B). In fact, quantitation of blood vessel branches confirmed a significant decrease in the number of arteries, with a reduction in branching from the third order onward (total number of arterial branches: Sham n=5: 282 ± 41; Obstructed n=5: 87 ± 41; P<0.01). Release of obstruction at 1 week, however preserved vascular morphology (Figure 2B) and the final number of arteries was similar to sham kidneys (Released n=3: 421 ± 136; compared with obstructed P<0.001; compared with sham NS, non-significant). In addition, contralateral kidneys of obstructed and released groups displayed compensatory growth with increased density of the arterial tree when compared with sham kidneys (Contralateral kidneys: Sham n=5: 342 ± 37; Obstructed n=5: 362 ± 18; Released n=3: 457 ± 116). These results indicate that significant repair and regeneration of the renal vasculature occurs subsequent to the surgical relief of the ureteral blockage.
Release of obstruction promotes regeneration of the renal vasculature
Using Toluidine Blue-stained semi-thin sections, we performed histological analysis on vascular structures in kidneys obstructed for 1 week and age/group matched sham kidneys (Figure 3). Interstitial micro-vascular damage was extensive at 1-week post-obstruction compared with the tubular damage (Figure 3). Capillary lumen dilatation accompanied by absence of pericyte coverage was noticed in the damaged areas of the obstructed kidneys, whereas sham kidney displayed intact pericyte coverage of the capillaries (Figure 3).
Renal micro vasculature damage at 1 week after obstruction
Observations of vascular structures on semi-thin sections in 3 WO kidneys revealed further degeneration of the renal vasculature and vascular rarefaction. The arterioles were dilated and accompanied with thinning of arteriolar smooth muscle lining. Detached pericyte-like cells were observed in the interstitial space. In addition, the endothelial cells were sparse and rounded up in several areas (Figure 4A,B). However, release of obstruction resulted in regeneration and restoration of normal distribution of endothelial cells as well as smooth muscle lining around the arteriolar walls. In the released kidneys, the morphology of the vasculature was similar to the one of the sham kidneys due to massive repair and remodeling (Figure 4A,B).
Relief of obstruction ameliorates obstructive vascular damage
Similarly, STEM image analyses revealed a marked damage and disintegration of endothelial cell lining of the vasculature in obstructed kidneys, with a remarkable improvement following the release of obstruction (Supplementary Figure S3A). We confirmed these observations using immunostaining for PECAM, a critical regulator of endothelial cell junctional integrity . Our results showed a prominent staining for PECAM in endothelial cells of arteries, arterioles, and interstitial and glomerular capillaries of sham kidneys indicating an intact endothelial lining of the vasculature. Obstructed kidneys showed a marked decrease in PECAM staining indicating loss of renal vessels and vascular rarefaction. In addition, abnormal dilated vascular structures suggest that endothelial cell integrity is severely compromised due to the obstruction damage (Supplementary Figure S3B). However, release of obstruction abrogates the progression of vascular anomalies post-obstruction and brings forth a significant regeneration and restoration of the renal vasculature similar to sham-operated kidneys (Supplementary Figure S3B).
Collectively our results suggest that onset of vascular damage may precede the tubular and interstitial damage during the obstruction injury. Moreover, release of obstruction results in regeneration and repair of the renal vasculature.
Release of obstruction promotes RBF
The excessive renal vascular damage during persistent obstruction and the remarkable repair post-release suggests an increase in RBF. Therefore, we used a contrast-enhanced US method and arterial spin-labeling MRI to compare the relative RBF estimate as a readout of vascular function in the mice that underwent surgeries.
Contrast-enhanced US is a validated method to measure RBF . Using this technique, we observed a significant decrease (64–73%) in RBF in 3 WO kidneys in comparison with the similar age group of sham-operated kidneys (Figure 5A). The RBF measurements were significantly higher in the left kidneys of sham group (n=3) compared with the obstructed group (n=3) in the whole kidney (Sham: 4.48 ± 1.58 b/cm2, Obstructed: 1.47 ± 0.54 b/cm2; P<0.05), cortex (Sham: 5.04 ± 1.51 b/cm2, Obstructed: 1.83 ± 0.84 b/cm2; P<0.05) and medulla (Sham: 2.84 ± 1.13 b/cm2, Obstructed: 0.76 ± 0.28 b/cm2; P<0.05).
RBF improves significantly following the release of obstruction
However, animals at 2 WR (n=5) displayed a significantly improved RBF in comparison with obstructed animals, both in the whole kidney and in regional measurements (whole kidneys: 7.84 ± 1.79 b/cm2, P<0.0001; cortex: 7.88 ± 1.98 b/cm2, P<0.0001; medulla 4.46 ± 0.43 b/cm2, P<0.0001). Though the mean RBF estimated following the release of obstruction was increased compared with sham-operated kidneys, statistical significance was observed (P<0.05) only in the medulla (Figure 5A). These results indicate that significant repair and regeneration of the vasculature post-release leads to restoration of normal levels of RBF.
We confirmed these results on RBF determinations from US imaging by steady state arterial spin-labeling MRI  at 5W after the release of obstruction (Figure 5B). Cortical RBF determinations in kidneys obstructed for 6W (n=3) showed a significant decrease in the blood flow compared with the similar age group of sham-operated kidneys (n=3) (Sham: 5.81 ± 0.59 ml/g/min; Obstructed: 2.30 ± 0.07 ml/g/min; P<0.001). Release of obstruction at 1 week (n=7) resulted in a remarkable increase in the RBF determinations at 5W post release (Figure 6) when compared with obstructed kidneys and with similar levels to sham-operated kidneys (released kidneys: 4.86 ± 0.74 ml/g/min; compared with obstructed P<0.01; compared with sham NS, non-significant).
Relief of obstruction ameliorates obstructive tubular and interstitial damage
Thus our experimental results showing increases in RBF in 3 and 6W old animals tested by two independent methods clearly indicate that release of obstruction significantly improves vascular repair and regeneration and achieves a concomitant improvement in renal vascular function.
Release of obstruction results in the remodeling of renal tubular epithelium and interstitium
Histological analyses on Toluidine Blue-stained semi-thin kidney sections revealed an increase in interstitial matrix deposition already at 1 WO (Figure 3). By 3 WO, the kidneys displayed excessive matrix deposition and tubular degeneration (Figure 6A). Removal of obstruction remarkably ameliorated and reverted the tissue damage. The kidney morphology at 2 WR was similar to sham-operated mice (Figure 6A). STEM analyses of kidney sections at 3 weeks of post-natal life showed extensive subcellular changes such as loss of tubular cell mitochondria, endoplasmic reticulum, interdigitating lateral processes of the basal lamina and brush border, with accumulation of vacuoles and increased interstitial matrix deposition in the obstructed group. These changes were reversed when the obstruction was removed and the interstitium and tubular epithelium displayed a remarkable remodeling (Figure 6B).
Next we investigated whether obstructed kidneys show evidence of degeneration in fatty acid metabolism, as we observed excessive accumulation of lipid droplet-like structures in the Toluidine Blue-stained semi-thin kidney sections, in severe hydronephrotic regions of the obstructed kidneys (data not shown). We performed Oil Red staining to assess lipid accumulation during tubular degeneration in obstructed kidneys. Kidneys at 3 WO, showed a marked increase in cells positive for Oil Red staining whereas sham kidneys showed no staining (Supplementary Figure S4A). This indicates an increased lipid accumulation and suggests a defective fatty acid oxidation (FAO)in the damaged tubular epithelium. Release of obstruction prevented the progression of the tubular injury, as indicated by absence of Oil Red staining in released kidneys (Supplementary Figure S4A).
We also checked if the vacuoles seen in the tubular epithelium of obstructed kidneys (Figure 6B) were autophagic using the marker LC3B-II . Our results revealed increased autophagic activity in the tubular and interstitial cells during obstruction. Release of obstruction prevented this abnormal increase in autophagy (Supplementary Figure S4B). Next, we assessed the status of primary cilia during kidney injury and repair, as the primary cilium defines the epithelial phenotype of the renal tubules [30,31]. Sham-operated kidneys showed the presence of intact cilia, whereas degenerating tubules in 3 WO kidneys revealed loss of cilia (Supplementary Figure S4C). In addition, some of the intact tubular cells of the obstructed kidneys displayed an increase in the primary cilium length, indicating dysregulated ciliogenesis and loss of epithelial cell identity. Presence of primary cilia in the tubular cells post-relief similar to sham-operated kidneys indicate that relief of obstruction prevents the progression in the tubular injury and promotes tubular repair (Supplementary Figure S4C).
As expected, Masson’s trichrome staining showed the presence of interstitial collagen deposition after 1 WO, which further increased at 3 WO indicating the onset and progression of fibrosis due to obstructive injury (Supplementary Figure S5). By contrast, release of obstruction resulted in the resolution of interstitial fibrosis, from a partial recovery at 1 WR to a complete recovery at 2 WR (Supplementary Figure S5). Quantitation on the collagen positive fibrotic area confirmed these observations (Sham-3W n=3: 2.53 ± 0.94% Obstructed-3W n=3: 33.16 ± 5.42%, P<0.001; Released n=3: 9.95 ± 2.30% compared with Obstructed P<0.01 compared with Sham NS, non-significant). Contralateral kidneys were similar to sham-operated kidneys (data not shown). These results confirm our observations on interstitial matrix in semi-thin sections and indicate that release of obstruction facilitates recovery and protection from the progressive interstitial fibrosis due to obstruction.
Collectively, our results indicate that during obstruction the kidneys undergo extensive tubular and interstitial damage and release of obstruction brings forth a remarkable repair and remodeling of these compartments.
Release of obstruction promotes recovery from renal oxidative stress
It has been shown that during kidney injury due to ureteral obstruction there is an increase in oxidative stress [32–34]. We hypothesized that following the release of obstruction the improved vascular function and recovery in tubular damage will be accompanied by a decrease in oxidative stress. Various biomarkers of oxidative stress are increased during ureteral obstruction. We tested two candidate markers Heme oxygenase-1 (HO-1) [32,35] and 4-hydroxynonenal (4-HNE) proteins [36,37] by immunohistochemistry.
Increase in HO-1 signals was observed in kidneys at 3 WO. Interstitial cells surrounding the tubular epithelium and in the areas of fibrotic damage showed increased HO-1 signals in comparison with sham and 2 WR kidneys (Figure 7A). Similarly, immunostaining for 4-HNE showed expression in several tubular cells in the obstructed kidneys, whereas it was absent from the sham and released kidneys (Figure 7B). These results indicate that renal tissues are subjected to oxidative stress during obstruction injury, which is relieved with the release of obstruction.
Reduction in renal oxidative stress following the release of obstruction
We also explored the changes in the status of other factors such as hypoxia, FAO defects and mitochondrial dysfunction which are potential contributors to oxidative stress [38–42]. Immunostaining for Hif1α and Hif2α in 3 WO kidneys revealed increased signals for these proteins only in tubular and interstitial cells that are severely damaged during obstruction injury. However, these hypoxia-regulated proteins were absent from the sham and post-release kidneys (Supplementary Figure S6). These results indicate that tissues with increased damage during obstruction undergo hypoxia and relief of obstruction ameliorates this phenomenon.
Next, we performed q-RT-PCR on key regulators of FAO that are differentially regulated during CKD . Our results show that mRNA levels of carnitine palmitoyltransferase 1a, liver (Cpt1a) and carnitine palmitoyltransferase 2 (Cpt2) critical for the carnitine shuttle of fatty acids to the mitochondria are significantly reduced during persistent obstruction damage (Figure 8A). Furthermore, mRNA levels of Acyl-Coenzyme A oxidase 1, palmitoyl (Acox1) and Acyl-Coenzyme A oxidase 2, branched chain (Acox2) genes were also significantly reduced in obstructed kidneys (Figure 8A). Proteins encoded by these genes are critical regulators of peroxisomal fatty acid β-oxidation pathway . In addition to the genes involved in fatty acid metabolism, mRNA levels of their key transcriptional regulator complex PPARA–PPARGC1A are significantly reduced during obstruction injury (Figure 8A). PPARA–PPARGC1A complex is also important in the regulation of mitochondrial biogenesis. However, remarkable improvement in the gene expression was observed for all the genes tested following the release of obstruction. The levels in the post-released kidneys were similar to sham-operated kidneys (Figure 8A). Dysregulation of FAO genes affects fatty acid metabolism leading to intracellular lipid accumulation and cellular lipotoxicity. Our q-RT-PCR results are consistent with the increased lipid accumulation observed in the renal tubular epithelium during obstruction injury and the recovery after release of obstruction (Supplementary Figure S4A).
Differential regulation of fatty acid metabolism and mitochondrial dysfunction during obstruction damage and recovery by qRT-PCR
q-RT-PCR for the mitochondrial related transcripts nuclear respiratory factor 1 (Nrf1), nuclear factor, erythroid derived 2, like 2 (Nrf2), Transcription factor A, mitochondrial (Tfam), Cytochrome c oxidase subunit 4I1 (Cox4), and Parkin RBR E3 ubiquitin protein ligase (Parkin2) involved in mitochondrial biogenesis and function [45,46] showed a significant decrease in obstructed kidneys indicating a severe mitochondrial dysfunction in the damaged cells. Release of obstruction resulted in a significant increase in the mRNA for all these genes compared with obstructed tissues (Figure 8B). These results indicate that normal mitochondrial function is perturbed in obstructed kidneys and defective mitochondrial function activates the onset of oxidative stress . Removal of obstruction facilitates recovery of the mitochondrial damage by improving the expression of genes critical for normal mitochondrial function, and thus resulting in the reduced oxidative stress in the damaged cells. These results are in agreement with the severe mitochondrial damage observed in the STEM images from obstructed kidneys and the remarkable regeneration of mitochondria observed post-release (Figure 6B).
Collectively, these results indicate that there is an increase in oxidative stress during kidney injury in neonatal pUUO. Accumulation of lipids along with mitochondrial dysfunction in the obstructed kidneys could contribute to this pathology. Release of obstruction alleviates the mitochondrial damage leading to a reduction in oxidative stress with tissue regeneration.
Foxd1-positive, stromal-derived cells expand and change their fate to putative myofibroblasts during pUUO damage
Foxd1 marks the stromal cell precursors that give rise to all renal vascular smooth muscle cells, renin cells, mesangial cells, and interstitial pericytes . Using Foxd1Cre;mTmG mice, we followed the distribution of cells from the Foxd1 lineage at various time points after obstruction and release of obstruction (Figure 1A).
As shown in Figure 9, at 1 and 3 WO there was a significant expansion of GFP+ interstitial cells in kidneys with moderate (index 2) and severe (index 3 and above) hydronephrosis. Surgical release of the obstruction resulted in tissue repair and regeneration as indicated by a marked decrease in the GFP+ interstitial cell area (Figure 9A,B). The extent of recovery increased with increase in time after the release of obstruction and was inversely correlated to the severity of damage at the time of release (Figure 9A). Quantitation on cumulative GFP+ interstitial cell area confirmed these observations (Figure 9B). One and three WO caused a significant increase in GFP+ interstitial area compared with sham kidneys (Sham-3W: 13.98 ± 2.70% (n=5) compared with obstructed-1W: 69.30 ± 3.34% (n=3), P<0.001; compared with obstructed-3W: 65.40 ± 2.85% (n=5), P<0.001). However, in 2 WR kidneys the GFP+ area was similar to sham surgery (Post-release-2W: 20.64 ± 4.68 (n=4) compared with obstructed-1W, P<0.01; compared with obstructed-3W, P<0.0001; compared with Sham, NS, non-significant). The GFP+ interstitial cell distribution in contralateral kidneys with or without the release was not different from the sham group (data not shown). In addition, qRT-PCR showed no significant changes in Foxd1 gene expression (Figure 9C). Our results indicate that changes observed in GFP+ Foxd1 lineage cells are not due to the activation of Foxd1 gene expression during kidney damage and repair.
Foxd1-derived GFP+ interstitial pericytes expand during pUUO damage
Immunostaining for PDGFRβ revealed an increase in interstitial pericytes at 3 WO, which was resolved at 2 WR (Figure 10). Quantitation of PDGFRβ positive areas showed an 85% increase in the obstructed kidneys (n=3) compared with sham kidneys (n=3) (Sham: 6.75 ± 2.65%; Obstructed: 45.13 ± 5.46%; P<0.001). However, PDGFRβ signals significantly decreased in 2 WR kidneys (n=3) and were similar to sham levels (Released: 7.28 ± 2.58%; comapred with obstructed, P<0.001; compared with sham, NS, non-significant). In addition, the staining pattern of PDGFRβ positive interstitial pericytes during obstruction and release was similar to the distribution of Foxd1-derived GFP+ interstitial cells suggesting that the latter are of pericyte origin.
Expansion of PDGFRβ positive cells during obstruction injury
α-SMA, a marker for activated myofibroblasts, was significantly increased in the renal interstitium of 3 WO kidneys (Figure 11A). In addition, the interstitial α-SMA co-localized with most of the expanded GFP+ interstitial cells in Foxd1Cre;mTmG kidneys. However, following the release of obstruction, interstitial α-SMA decreased with expression restricted to vascular mural cells as in sham kidneys (Figure 11A). Moreover, qRT-PCR analysis in 3 WO kidneys showed a significant increase in α-SMA expression compared with sham kidneys. In contrast, released kidneys displayed levels similar to shams (Figure 11B). Similarly, transforming growth factor, β 1 (TGF-β1) mRNA levels significantly increased in obstructed kidneys, but decreased to the levels of sham kidneys following the release of obstruction (Figure 11C). These results suggest that Foxd1-derived interstitial pericytes undergo cell fate changes and differentiate into putative myofibroblasts during obstruction by acquiring α-SMA due to increases in TGF-β1. Release of obstruction abrogates these fate changes by preventing the up-regulation of TGF- β1 and α-SMA expression.
Release of obstruction reverses pericyte cell fate changes to α-SMA positive myofibroblasts
Release of obstruction promotes recovery of Six2-derived nephron epithelium
Six2 is a marker for nephron progenitor cells in the cap mesenchyme and Six2 lineage cells are present along the entire nephron in sham-operated kidneys (Figure 12A). Ureteral obstruction in Six2Cre;mTmG mice induced a loss of GFP+ tubular epithelium proportional to the hydronephrosis index (Figure 12A). By contrast, with the release of obstruction, the injury and progressive disappearance of Six2-derived tubules was averted (Figure 12A). The nephron integrity of the contralateral kidneys was maintained (data not shown).
Release of obstruction prevents Six2- derived nephron epithelial damage
Damage to cap mesenchyme-derived proximal tubules resulted in the formation of atubular glomeruli (Figure 12A). Atubular glomeruli in Six2Cre;mTmG kidneys were identified by the absence of Lotus tetragonolobus lectin, which stains the proximal tubular epithelial cells at the glomerulo–tubular junction (Figure 12B). The fraction of atubular glomeruli (Figure 12C) increased in severely obstructed kidneys. Following the relief of obstruction, the number of atubular glomeruli decreased to levels close to the ones of sham kidneys. (Sham n=3: 1.37 ± 0.42 × 10−6/µm2 Obstructed n=3: 6.32 ± 1.8 × 10−6/µm2; P<0.01; Released n=3: 2.89 ± 1.14 × 10−6/µm2). These results indicate that release of obstruction preserves the glomeruli from undergoing severe damage at the glomerulo–tubular junction. GFP+ Six2 lineage cells were restricted to the nephron epithelium, indicating that cap mesenchyme-derived nephron epithelium does not transdifferentiate to other cell types during kidney repair. qRT-PCR analysis showed no significant changes in Six2 gene expression during obstruction and after release (Figure 12D).
Release of obstruction reverses HoxB7-derived collecting duct loss
The fate of UB-derived cells was determined in HoxB7Cre;mTmG mice, wherein collecting ducts are labeled with GFP, following the strategy shown in Figure 1A. At 1 WO GFP+ tubular cells in the kidney cortex were smaller in size and the collecting duct area fraction presented a decreasing trend in comparison with sham kidneys suggesting the onset of tubular degeneration (Figure 13A,B). With persistent obstruction (3 WO) the tubular damage increased further resulting in severe hydronephrotic kidneys with compression of the renal medulla and virtually a complete loss of collecting ducts during severe injury (Sham n=3: 4.66 ± 0.29% 1W Obstructed n=3: 3.55 ± 0.20% 3W Obstructed n=3: 1.07 ± 0.31% compared with Sham P<0.05). Release of obstruction prevented the extensive loss of collecting ducts triggered by the obstruction (Released n=3: 4.84 ± 0.49% compared with 3W Obstructed P<0.05). Significant increase in the GFP positive collecting duct area post-release compared with post-obstruction indicates a remarkable recovery in the tubular damage and a significant protection from tubular loss. The distribution of GFP+ collecting ducts in the contralateral kidneys of obstructed and released groups was similar to sham kidneys (data not shown).
Release of obstruction prevents HoxB7-derived collecting duct loss
The presence of GFP+ UB-derived cells was observed only in the collecting ducts and not in any other tissue domain during obstruction and following the release of obstruction in Hoxb7Cre;mTmG mice. These results indicate that UB derived collecting duct epithelial cells do not contribute physically to the interstitial fibrosis due to ureteral obstruction. In addition, qRT-PCR analyses showed no significant changes in HoxB7 gene expression indicating that changes in the number of GFP+ tubular epithelial cells is not due to changes in the Cre expression during kidney damage and repair (Figure 13C).
The fate of podocyte derived cells during UUO damage and recovery
Contribution of podocyte-derived cells to renal tissue damage and repair was analyzed by crossing podocyte-specific Cre mice with the Cre reporter mTmG mice. All the surgical procedures were performed as described in Figure 1A. Lineage tracing in 3 weeks old animals showed that podocyte lineage (GFP+) cells were restricted to glomerular podocytes regardless of the presence or release of obstruction (Figure 14A). qRT-PCR expression analyses for v-maf musculoaponeurotic fibrosarcoma oncogene family, protein B (Mafb), a podocyte progenitor cell marker  showed no significant changes due to obstruction and release of obstruction (Figure 14B).
The fate of podocyte-derived cells during kidney damage and recovery
Neogenesis and de-differentiation during repair and regeneration post-obstruction
Cell proliferation was analyzed by quantitating phosphohistone-positive mitotic cells. There was a significant increase in actively dividing cells in 3 WO kidneys (n=3) compared with 3W sham kidneys (Sham n=3: 0.31 ± 0.08 × 10−5/µm2 3W Obstructed n=4: 1.11 ± 0.15 × 10−5/µm2; P<0.01). Proliferating mitotic cells were observed both in the tubular and interstitial compartments of the obstructed kidneys. Cell proliferation in post-released kidneys at 2 WR was similar to the sham-operated group (Released n=3: 0.39 ± 0.18 × 10−5/µm2). This may indicate proliferation of differentiated cells, de-differentiation followed by proliferation and/or neogenesis . Kidneys from obstructed and released groups of animals from Foxd1Cre;mTmG cross showed a discrete population of cells positive for the embryonic stem cell markers Oct 4 or Nanog and these cells were also double positive for GFP and red fluorescent protein (RFP), consistent with neogenesis. Though the double positive cells were present in all groups, signals for embryonic stem cell markers were evident only in the obstructed and released kidneys (Supplementary Figures S8 and S9).
SRY (sex determining region Y)-box 9 (Sox9) positive cells exhibit progenitor-like properties regulating regeneration of renal tubular epithelium in adult mice . Tubular Sox9-positive cells increased in the obstructed kidney, and decreased following the release of obstruction (Supplementary Figure S10).
These findings suggest the possible contribution of neogenesis accompanied with de-differentiation of more mature renal cells to pluripotent cells (or pluripotent-like cells) during kidney repair and regeneration.
In the present study, we showed that: (i) during ureteral obstruction the neonatal kidneys undergo extensive vascular damage and release of obstruction results in regeneration of renal arterioles. (ii) The remarkable regeneration of the renal vasculature following the obstruction relief promotes RBF. (iii) The release of obstruction resolves the damage to renal epithelial and interstitial cells, likely by decreasing hypoxia, renal oxidative stress, mitochondrial and FAO dysfunction. (iv) Foxd1-positive stromal-derived microvascular pericytes change their fate to putative myofibroblasts, thereby contribute to interstitial fibrosis in obstructed kidneys, and release of obstruction reverses these cell fate changes. (v) HoxB7 and Six2-derived tubular epithelial cells and podocyte-derived cells do not transdifferentiate to collagen producing myofibroblasts, but are lost during pUUO and can regenerate after release of obstruction.
Our current study reveals the capacity of the developing mammalian kidney to resume vascular and nephron development and maturation following the release of pUUO created during nephrogenesis. Recovery is more complete when obstructive injury is moderate at the time of release, as over 96% of kidneys with moderate hydronephrosis recovered near-normal architecture, whereas only 36% of kidneys with severe hydronephrosis recovered. The pUUO model reproduces many characteristics of congenital ureteropelvic junction obstruction, the most common obstructive anomaly of the developing urinary tract, which also presents as a spectrum from mild-to-severe obstruction . During neonatal pUUO, kidney vascular and tubulo-interstitial cells respond by interrupting normal development, and by shifting cellular differentiation to a pathway that leads to transformation of pericytes to myofibroblasts (Figure 15). Transition of myofibroblasts could exacerbate the renal damage by microvascular degeneration and interstitial collagen deposition. In addition, persistent obstruction leads to excessive nephro-vascular damage and loss (Figure 15). In contrast with the extensive vascular damage with stunting of renal arterial branching that results in decreased RBF during obstruction, release of obstruction resulted in a remarkable repair and regeneration of the renal vasculature (Figure 15). More importantly, our current study also indicates that the remarkable vascular regeneration observed post-release also improved the RBF achieving levels similar to sham kidneys using two independent techniques at 2 and 5W post release. A previous study done in adult mice where RBF was measured as a ratio of RPF (renal plasma flow) to 1-hematocrit showed only 56% recovery after release . These differences suggest that the recovery potential of the renal vasculature in the developing kidney is significantly higher than that of the adult kidney.
A proposed model of kidney injury and repair during obstruction and post-release in neonatal mouse kidneys
Furthermore, the contralateral kidneys of obstructed animals showed increase in the density of the arteriolar branches indicating a morphogenetic compensatory mechanism. The rate of compensatory kidney growth depends on duration and severity of injury in the obstructed kidneys [14,54] and relief of obstruction decreased this phenomenon. The compensatory growth of the contralateral kidneys hitherto has been thought as a hypertrophic, maladaptive mechanism . Ours is the first report showing that in fact the compensatory effect of the contralateral kidneys is a developmental phenomenon, as the renal vasculature displays increased branching morphogenesis. These results favor the process of angiogenesis rather than vasculogenesis. Nevertheless, the role of angioblasts in vascular regrowth remains to be explored. In addition, the role of pro-angiogenic molecules, factors promoting vascular myogenesis, and arteriogenesis [56–58] in the interstitial milieu post-injury and release is not known and needs to be characterized. Identifying the cellular and molecular mechanisms promoting microvascular repair and regeneration will be critical for designing treatment strategies to hasten kidney repair in patients with CKDs .
Recent studies in the neonatal mouse demonstrated that proximal tubule cells respond to UUO within the first 7 days of obstruction by increased oxidative stress, mitochondrial swelling, vacuolization, and cell death . The tubular response to obstruction is mediated by mechanical stretching of the epithelial cells, metabolic stress induced by mitochondrial injury, macrophage infiltration, hypoxia, and marked up-regulation of TGF-β1 . These factors also affect the redox state in the tissues and production of reactive oxygen species. Our current study confirms these observations and also provides additional information that release of obstruction preserves the tubular cells from undergoing: (i) extensive loss of primary cilia, mitochondria and other subcellular structures, (ii) dysregulated FAO, (iii) hypoxia, and (iv) oxidative stress. In addition to cell fate changes, increasing levels of TGF-β1 stimulates oxidative stress and cell death whereas inhibition of oxidative stress ameliorates tubular injury and interstitial fibrosis . The decrease in TGF-β1 levels observed in the post-release kidneys likely contributes to remodeling of vasculature and nephrons. Identification of the upstream molecular regulators promoting the recovery of tissue damage following release of ureteral obstruction may lead to novel therapeutic strategies for obstructive nephropathy and other CKDs.
TGF-β1 is the primary factor for the differentiation of pericytes to myofibroblasts and fibrosis activation in most CKDs [61–65]. In the current study both TGF-β1 and α-SMA expression levels were increased post-obstruction and normalized following release indicating that relief of obstruction reverts the injury and damage. As the microvasculature is stabilized by the interaction of pericytes with endothelial tubes [66–68] we predict that inhibition of TGF-β1 post-release of obstruction could promote reversal of cell fate changes, renewal of the pericyte population and the recruitment of pericytes to arteriolar and capillary walls. There is mounting evidence for the importance of stromal cells in balancing the switch between regeneration and fibrotic repair . Elucidation of gene regulatory networks activated in the unique microenvironment of the developing kidney is likely to provide new insight into the regenerative mechanisms.
Our study in neonatal mice confirms that Foxd1 derived cells are the main contributors to the formation of myofibroblasts similar to adult kidneys [15,70]. Whether there is any contribution of circulating Foxd1-derived cells in myofibroblast formation in obstructed kidneys remains to be determined. We found no direct contribution of tubular (nephron and collecting duct), podocyte, renin progenitors (data not shown) and their descendants to the formation of myofibroblasts or the progression of interstitial fibrosis. This suggests that stromal cells in the developing neonatal and early post-natal kidney while still capable of differentiating into their derivatives can also activate a cellular program similar to the one of the adult kidneys in response to injury. Injury to nephrons and the interstitium have also been viewed as early attempts at repair  allowing for regeneration when the obstruction is released. However, this hypothesis needs to be proven experimentally. From an evolutionary perspective, allocation of energy for maintaining nonfunctioning nephrons must be limited, accounting for ‘failed repair’ during persistent obstruction . Importantly, compared with the adult kidney, enhanced renal recovery of the post-obstructed neonatal kidney is consistent with greater allocation of energy to both growth and regeneration in the pre-reproductive phase of the life cycle.
Similar to the adult mouse models [15,73,74], the current study in neonatal mice demonstrates an increase in cell proliferation and no dilution of the genetic labeling in tissues undergoing repair. Moreover, presence of GFP and RFP double positive cell clusters with stem cell markers POU domain, class 5, transcription factor 1 (OCT4) or Nanog in the present study raises the possibility of neogenesis, MRPCs (multi potent renal progenitor cells) and VSELs (very small embryonic-like stem cells) in tissue repair [75–77], similar to the formation of neoblasts or blastema that gives rise to differentiated cells during regeneration in planarians, fish and Axolotl [78–81]. This regeneration pathway may be suppressed by the presence of severe ureteral obstruction during nephron maturation but could be unmasked by release of obstruction.
In summary, using a pUUO model in neonatal mice, our study fills an important gap in the field and provides compelling evidence on the origin of cells directly contributing to the tissue damage and regeneration in neonatal obstructive nephropathy. Our study also underscores the importance of timely release of obstruction in the developing kidney  and the crucial role of the vasculature and associated nephrons in the tissue repair following the release of obstruction. Identifying the mechanisms and molecular targets mediating the repair and regeneration following the release of obstruction would be of paramount importance for the development of therapeutic interventions in the prevention and/or treatment of CKDs in pediatric and adult patients.
Congenital obstructive nephropathy is the leading cause of CKD in children. Using a mouse model that replicates obstruction in the mid-trimester human fetus, we identified the major renal progenitors and their descendants that contribute to kidney damage and regeneration during obstruction and after its release, respectively.
We observed extensive cell fate changes in stromal cell derivatives and nephron-vascular loss during obstruction. Surgical correction of the obstruction reverses cellular damage and cell fate changes and the kidney vasculature and tubular-interstitial compartments regenerate. The remarkable structural and functional recovery and regeneration following release of the obstructed neonatal kidney suggests that surgical correction of congenital obstructive nephropathy should not be delayed.
Deciphering the cellular and molecular mechanisms involved in nephron-vascular repair and regeneration post-release of obstruction has potential therapeutic implications for infants and children and the expanding adult population suffering from CKD.
We thank Dr. Silvia Medrano and Dr. Brian Belyea for reading the manuscript and providing suggestions and the technical assistance of Danielle Stumbo, Tiffany Southard, and Xiuyin Liang. We thank the UVA molecular imaging core facilities for MRI scans performed in the current study.
The authors declare that there are no competing interests associated with the manuscript.
This work was supported by the National Institutes of Health [grant numbers DK091330, DK096373, DK116196 (to M.L.S.S.-L.)].
V.K.N. designed the study; carried out surgeries and experiments; analyzed the data; drafted and revised the paper. M.L. carried out surgeries and experiments. S.S. image analyses on MRI scans for RBF measurements. J.C.G image analyses on contrast-enhanced US study for RBF measurements. A.L.K. provided technical expertise and material support for contrast-enhanced US study for RBF measurements. F.H.E. provided technical expertise and material support for steady-pulsed arterial spin-labeling MRI for RBF measurements. R.L.C. and R.A.G. edited and revised the manuscript; M.L.S.S.-L. designed the study, edited and revised the manuscript.
α-smooth muscle actin
chronic kidney disease
fatty acid oxidation
Forkhead Box D1
hypoxia-inducible factor 1-α
hypoxia-inducible factor 2-α
membrane-targetted tandem dimer Tomato
platelet-derived growth factor receptor, β polypeptide
platelet endothelial cell adhesion molecule-1
partial unilateral ureteral obstruction
quantitative reverse-transcription PCR
renal blood flow
red fluorescent protein
Sine oculis homeobox homolog 2
SRY (sex-determining region Y)-box 9
steady-pulsed arterial spin labeling
transforming growth factor, β 1
week after obstruction
weeks after release