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Keywords: hepatocyte
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Biochem J (2014) 463 (2): 201–213.
Published: 22 September 2014
... conclude that MAL2 and the constitutively active STK16 function to sort secretory soluble cargo into the constitutive secretory pathway at the TGN ( trans -Golgi network) in polarized hepatocytes. 1 Present address: Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD...
Includes: Supplementary data
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Biochem J (2014) 458 (1): 95–107.
Published: 20 January 2014
... constitutively active, in hepatocytes CAR is normally held quiescent through a tethering mechanism in the cytosol, anchored to a protein complex that includes several components, including heat-shock protein 90. Release and subsequent nuclear translocation of CAR is triggered through either direct binding...
Includes: Supplementary data
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Biochem J (2012) 443 (1): 193–203.
Published: 14 March 2012
... to enzyme inactivation by decreasing the affinity for both UDP-Glc (UDP-glucose) [assayed in the absence of Glc-6- P (glucose-6-phosphate)] and Glc-6- P (assayed at low UDP-Glc concentrations). Incubation of freshly isolated rat hepatocytes with the pharmacological AMPK activators AICA riboside (5...
Includes: Supplementary data
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Biochem J (2011) 439 (3): 497–504.
Published: 13 October 2011
... © The Authors Journal compilation © 2011 Biochemical Society 2011 apical targeting cholesterol epithelium hepatocyte lipid raft myelin and lymphocyte protein (MAL) Isolation of low-buoyancy membrane fractions was performed as described in [ 24 ]. WIF-B cells were rinsed in ice...
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Biochem J (2011) 437 (3): 477–482.
Published: 13 July 2011
...Marie-Laure Island; Nadia Fatih; Patricia Leroyer; Pierre Brissot; Olivier Loreal Hepcidin, a hormone mainly synthesized by hepatocytes and secreted in plasma, controls iron bioavailability. Thus, by inducing the internalization of the iron exporter ferroportin, it regulates iron release from...
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Biochem J (2009) 423 (3): 303–314.
Published: 12 October 2009
.... HCV is an enveloped virus bearing two surface glycoproteins, E1 and E2. It only infects humans through blood transmission, and hepatocytes are its only target cells. Hepatic trabeculae are formed by hepatocyte rows surrounded by sinusoid capillaries, irrigating hepatic cells. Hepatocytes are polarized...
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Biochem J (2008) 411 (1): 1–18.
Published: 13 March 2008
... of these cells in diseased liver originate from the bone marrow. In addition, fibrogenic fibroblasts may also be generated through liver epithelial (hepatocyte and biliary epithelial cell)–mesenchymal transition. Whatever their origin, it is clear that fibrogenic fibroblast activity is sensitive to (and may...
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Biochem J (2007) 404 (3): 499–507.
Published: 29 May 2007
... in cell energy homoeostasis. In the present study, we investigated the effects of AICA riboside on mitochondrial oxidative; phosphorylation. AICA riboside was found to dose-dependently inhibit the oligomycin-sensitive J O 2 (oxygen consumption rate) of isolated rat hepatocytes. A decrease in P i...
Includes: Supplementary data
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Biochem J (2006) 398 (3): 371–380.
Published: 29 August 2006
... 2006 apoptosis cyclo-oxygenase (COX) hepatocyte hydrodynamic transfection liver prostaglandin COX (cyclo-oxygenase) enzymes catalyse the first step in the biosynthesis of PGs (prostaglandins) and thromboxanes [ 1 , 2 ]. The COX-1 isoform is constitutively expressed in many tissues [ 3...
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Biochem J (2006) 395 (1): 49–55.
Published: 15 March 2006
... hepatocytes. The intracellular fluorescence was not only quenched by an addition of a highly lipophilic 8-hydroxyquinoline–iron(III) complex but also was dequenched by the addition of an excess of the membrane-permeable iron chelator CP94 (1,2-diethyl-3-hydroxypyridin-4-one). The time course of uptake of iron...
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Biochem J (2006) 394 (2): e3.
Published: 10 February 2006
...Frank J. Gonzalez IL-1β (interleukin-1β) treatment of hepatocytes results in an NF-κB (nuclear factor-κB)-mediated activation of the iNOS (induced nitric oxide synthase) gene, and this increase in gene expression is further augmented by oxidative stress. Oxidative stress alone has no influence...
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Biochem J (2005) 385 (1): 165–171.
Published: 14 December 2004
... repeat) proteins. Insulin treatment increased EIIH mRNA levels in the hepatocytes of suckling, fasted adult and STZ (streptozotocin)-treated diabetic rats, where insulin was required to maintain the basal level of EIIH expression. EIIH expression was induced during the suckling/weaning transition...
Includes: Supplementary data
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Biochem J (2003) 376 (2): 465–472.
Published: 01 December 2003
... and chlorpromazine. Also, the induction of CYP2B10 mRNA by oestrogens was less pronounced in mouse primary hepatocytes. Yeast two-hybrid assays indicated that, unlike androstenol and the established activators, oestrogens attracted both nuclear receptor co-repressors and co-activators to the mCAR ligand-binding...
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Biochem J (2001) 354 (3): 531–537.
Published: 08 March 2001
...Thomas KIETZMANN; Yvonne CORNESSE; Katja BRECHTEL; Said MODARESSI; Kurt JUNGERMANN The cDNAs of three hypoxia-inducible factor (HIF) α-subunits were cloned from RNA of primary rat hepatocytes by reverse transcriptase PCR. All three cDNAs encoded functionally active proteins, of 825, 874 and 662...
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Biochem J (2000) 352 (3): 929–933.
Published: 08 December 2000
...Charles E. ADKINS; Frank WISSING; Barry V. L. POTTER; Colin W. TAYLOR Adenophostin A, the most potent known agonist of inositol 1,4,5-trisphosphate (Ins P 3 ) receptors, stimulated 45 Ca 2+ release from the intracellular stores of permeabilized hepatocytes. The concentration of adenophostin...
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Biochem J (2000) 351 (3): 811–816.
Published: 24 October 2000
...Roger R. GOMIS; Juan C. FERRER; Joan J. GUINOVART We have used recombinant adenoviruses (AdCMV-RLGS and AdCMV-GK) to overexpress the liver isoforms of glycogen synthase (GS) and glucokinase (GK) in primary cultured rat hepatocytes. Glucose activated overexpressed GS in a dose-dependent manner...
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Biochem J (2000) 350 (3): 685–692.
Published: 08 September 2000
... are not well known. However, given the central role of the liver in amino acid metabolism, we developed a rat primary hepatocyte model in which homocysteine (and cysteine) production and export were examined. The dependence of homocysteine export from incubated hepatocytes on methionine concentration fitted...
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Biochem J (2000) 348 (1): 215–222.
Published: 09 May 2000
... to the cytoplasm after brief perfusion of the liver with a perfusate containing 20 mM glucose [8]. Using isolated hepatocytes, Agius and Peak showed that the fraction of total glucokinase released in soluble form after cell permeabili- zation with low concentrations of digitonin increased after Abbreviations used...
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Biochem J (1999) 339 (1): 111–117.
Published: 25 March 1999
... only slightly increased in liver of rats refed with a high-carbohydrate diet or after partial hepatectomy. Whereas the expression of Hex mRNA was detected in hepatocytes isolated from adult rat liver and also in highly differentiated hepatoma cells, no Hex mRNA was detected in poorly differentiated...
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Biochem J (1999) 337 (3): 497–501.
Published: 25 January 1999
...John W. PHILLIPS; Debra C. HENLY; Michael N. BERRY The stimulation of glucose phosphorylation in isolated hepatocytes by low fructose concentrations is transient due to the rapid metabolism of fructose. To prolong this stimulatory effect fructose was enzymically generated in the incubation medium...