The mPTP (mitochondrial permeability transition pore) is a non-specific channel that is formed in the mitochondrial inner membrane in response to several stimuli, including elevated levels of matrix calcium. The pore is proposed to be composed of the ANT (adenine nucleotide translocase), voltage-dependent anion channel and cyclophilin D. Knockout studies, however, have demonstrated that ANT is not essential for permeability transition, which has led to the proposal that other members of the mitochondrial carrier protein family may be able to play a similar function to ANT in pore formation. To investigate this possibility, we have studied the permeability transition properties of BAT (brown adipose tissue) mitochondria in which levels of the mitochondrial carrier protein, UCP1 (uncoupling protein 1), can exceed those of ANT. Using an improved spectroscopic assay, we have quantified mPTP formation in de-energized mitochondria from wild-type and Ucp1KO (Ucp1-knockout) mice and assessed the dependence of pore formation on UCP1. When correctly normalized for differences in mitochondrial morphology, we find that calcium-induced mPTP activity is the same in both types of mitochondria, with similar sensitivity to GDP (~50% inhibited), although the portion sensitive to cyclosporin A is higher in mitochondria lacking UCP1 (~80% inhibited, compared with ~60% in mitochondria containing UCP1). We conclude that UCP1 is not a component of the cyclosporin A-sensitive mPTP in BAT and that playing a role in mPTP formation is not a general characteristic of the mitochondrial carrier protein family but is, more likely, restricted to specific members including ANT.
Mitochondria possess a Ca2+-inducible non-specific pore that allows the free movement of solutes of less than ~1.5 kDa across the mitochondrial inner membrane. Known as the mPTP (mitochondrial permeability transition pore), its activity is not compatible with the conventional chemiosmotic processes of mitochondria and causes matrix swelling, the collapse of protonmotive force and ATP depletion, leading to compromised cell viability. The mPTP has a clear involvement in necrotic cell death induced by calcium overload and oxidative stress, and may play a physiological role in the release of signalling factors from the mitochondrial intermembrane space during apoptosis (see [1–4] for reviews).
Although the components of the mPTP are yet to be conclusively identified, pore formation is proposed to involve cyclophilin D, ANT (adenine nucleotide translocase) and VDAC (voltage-dependent anion channel) [1,2]. Cyclophilin D is a mitochondrial-matrix-located peptidylprolyl cis–trans isomerase that associates with the mitochondrial inner membrane during conditions that promote permeability transition [5,6]. It is believed to induce a conformational change in a membrane protein to bring about pore formation . The drug cyclosporin A inhibits cyclophilin D and is the classic inhibitor of the permeability transition [8,9]. Mice lacking cyclophilin D do not undergo cyclosporin A-sensitive permeability transition but still form mPTP at higher matrix Ca2+ concentrations [10–12], indicating that cyclophilin D is not an essential component but may act to sensitize the Ca2+ trigger site of the pore.
ANT has long been implicated in mPTP (see ) and is believed to be the membrane target of cyclophilin D. Ligands of ANT that promote the ‘c’ (carboxyatractyloside) or ‘m’ conformation (bongkrekic acid) stimulate or inhibit mPTP respectively. Matrix ADP binding to ANT also inhibits mPTP and may be key in the mechanism by which mPTP formation is inhibited by Δψ [7,13]. Importantly, a direct interaction between cyclophilin D and ANT has been demonstrated using cyclophilin D affinity columns and co-immunoprecipitation [3,14,15]. Strong evidence that supports ANT as the primary component of mPTP is provided by reconstitution studies. In response to high Ca2+ concentrations, phospholipid membranes containing purified ANT generate a non-specific pore that may represent a basic mPTP structure [16,17]. Reconstitution of ANT as part of a cyclophilin D–ANT–VDAC complex, recovered from a cyclophilin D affinity column, also results in Ca2+-inducible pore formation that, importantly, can be inhibited by cyclosporin A . The exact influence of VDAC in mPTP formation is not clear although mitochondria from mice ablated of VDAC1 exhibit unchanged permeability transition properties, suggesting that this isoform, at least, plays only a minor role .
Mouse mitochondria lacking ANT still exhibit cyclosporin A-sensitive mPTP formation, indicating that ANT is not an essential component of mPTP . A possible explanation of this finding is that other proteins, similar to ANT, can perform the same structural role. ANT is typically the most abundant member of a large family of mitochondrial carrier proteins that share general structural features . Formation of cyclosporin A-sensitive mPTP may be a general feature of this family and the well-established influence of ANT merely a reflection of its abundance over other mitochondrial carriers. To address this possibility, we have studied the permeability transition properties of BAT (brown adipose tissue) mitochondria from mice kept at 21°C, which are atypical in that they contain a mitochondrial carrier protein, UCP1 (uncoupling protein 1), at concentrations comparable with ANT . Using an improved spectroscopic assay of mitochondrial swelling, we have quantified Ca2+-induced mPTP formation in BAT mitochondria isolated from both wild-type and Ucp1KO (Ucp1-knockout) mice. When correctly normalized for differences in the relationship between mitochondrial absorbance and matrix volume, we find that mPTP formation in Ucp1KO mitochondria is the same as in wild-type mitochondria, but the fraction sensitive to cyclosporin A is increased. These results indicate that UCP1 does not catalyse cyclosporin A-sensitive mPTP and ANT's role in mPTP is not a general characteristic of the mitochondrial carrier protein family.
Male and female mice were housed at 21±2°C, 57±5% humidity, 12 h/12 h light/dark cycle, with standard chow and water ad libitum, following the U.K. Home Office Guidelines for the Care and Use of Laboratory Animals. Ucp1KO  and wild-type sibling paired mice were used at age 7–12 months. Ucp1 ablation was confirmed by Western-blot analysis of the protein and PCR analysis of the genomic loci.
Isolation of mitochondria
BAT mitochondria were isolated as described in  but with the omission of EGTA in the final resuspension medium. Mitochondrial protein was estimated by the biuret method.
BAT mitochondria (0.15 mg) were stirred in 1.5 ml of reaction medium [0.25 M mannitol, 1 mM nitrilotriacetic acid (tetraethyl ammonium salt), 20 mM Mops buffer and 10 mM Tris buffer, pH 7.2 at 25°C] and the absorbance at 520 nm was followed by using a PerkinElmer lambda 18 spectrophotometer. To fully de-energize mitochondria and equilibrate Ca2+ across membranes, a cocktail of 0.2 μM rotenone, 0.2 μM antimycin A and 2 μM A23187 was added after mitochondrial addition, followed by 1.3 μM FCCP (carbonyl cyanide p-trifluoromethoxyphenylhydrazone). Swelling was induced by the addition of calcium gluconate to give the free Ca2+ concentration required under buffered conditions. Free calcium concentrations in the reaction medium were determined by following Calcium Green-5N (Molecular Probes, Invitrogen) fluorescence calibrated to calcium standards in reaction medium lacking nitrilotriacetic acid. Alternatively, immediate swelling was achieved on addition of mitochondria to reaction medium in which mannitol was replaced by 0.25 M erythritol. Swelling associated with erythritol uptake, specifically, was estimated by subtracting equivalent values of A−1 obtained in the presence of mannitol medium. In all cases, A−1 data were fitted using exponentials to estimate the initial rates (r2≥0.99).
Mitochondrial lipids were extracted using chloroform and methanol, and the phospholipid phosphorus content was estimated as described in . Values given (see main text) are means (±S.E.M.) from five separate mitochondrial preparations.
RESULTS AND DISCUSSION
Time-resolved mPTP formation in isolated mitochondria has typically been assessed by monitoring the collapse of Δψ or by following the absorbance changes associated with the matrix volume changes that accompany solute uptake. With either approach, the use of energized mitochondria complicates mechanistic interpretation as any affect on mPTP may be indirect, via Δψ, particularly if UCP1 is involved. Also, neither approach is ideal for a quantitative analysis of the time course of mPTP formation. Mitochondrial absorbance measurements, for instance, suffer from a non-linear relationship with matrix volume that can vary between mitochondria from different sources. To address this deficit in methodology, we developed an improved spectroscopic method to quantify cyclosporin A-sensitive mPTP in BAT mitochondria under de-energized conditions.
Mitochondria behave as simple osmometers in that their matrix volume is proportional to the inverse osmolality of the support medium [25–27]. In accordance with previous reports , we find that the inverse of the apparent absorbance of BAT mitochondria, equilibrated in media of various osmotic strengths, also changed linearly with inverse osmolality of the medium (Figure 1, inset). When expressed as A−1 and in the range measured, therefore, absorbance measurements can be used quantitatively to report relative changes in mitochondrial matrix water content. Addition of 500 μM free Ca2+ (as calcium gluconate, the anion of which is not transported by UCP1 ) to BAT mitochondria pre-equilibrated in 0.25 M mannitol medium induced rapid swelling associated with the uptake of mannitol (trace a, Figure 1A). This activity was inhibited by cyclosporin A (trace b), confirming that it is a consequence of mPTP formation. Intriguingly, inhibition occurred in the absence of phosphate in the incubation medium, in contrast with the situation in liver mitochondria where mPTP inhibition by cyclosporin A is dependent on the presence of this anion (see ). Phosphate regulation of mPTP inhibition by cyclosporin A, therefore, may not occur in BAT mitochondria, or instead, may just be dependent upon the assay conditions used. Importantly, in our assay conditions, mitochondria were kept fully de-energized (see the Experimental section) to avoid indirect effects of conventional UCP1 activity on mPTP. Initial rates of Ca2+-induced swelling were linearly dependent on the free Ca2+ concentration and were ~60% sensitive to cyclosporin A (Figure 1B). This simple relationship suggests that our measurements do, indeed, report relative mPTP activities.
Calcium-induced cyclosporin A-sensitive swelling of de-energized BAT mitochondria
An initial assessment of mPTP formation in BAT mitochondria from Ucp1KO mice suggested that the rates of Ca2+-induced swelling were lower than in mitochondria from wild-type mice (traces b and a respectively, Figure 2A). Caution must be taken, however, as these differences could have been due to general differences in the light scattering properties of Ucp1KO and wild-type mitochondria that were unrelated to mPTP. Indeed, a preliminary assessment of the dependence of A−1 on osmolality−1 for Ucp1KO mitochondria indicated a linear, but shallower, relationship compared with wild-type mitochondria (results not shown). This suggests that the two mitochondrial populations were morphologically different and potentially exhibited different increments in A−1 for a specific amount of solute imported during permeability measurements.
Calcium- and erythritol-induced swelling of BAT mitochondria from wild-type and
To correct for these differences, we measured swelling rates induced by erythritol. Biological membranes are permeable to this sugar, which enters mitochondria independently of mPTP and other transporters (see ). Rates of permeation per mg of mitochondrial protein will depend on membrane lipid composition and will be proportional to the membrane surface area. Wildtype and Ucp1KO mitochondria have the same phospholipid fatty acyl group composition  and our estimates of mitochondrial lipid phosphorus (2.7±0.2 μg/mg of protein for wild-type mitochondria and 2.4±0.4 μg/mg of protein for Ucp1KO mitochondria), as a marker of total lipid, suggested that they do not have significantly different surface areas. Therefore the initial rate of erythritol entry into both mitochondrial types should be the same, regardless of A−1 signal. Upon the addition of mitochondria to 0.25 M erythritol medium, it can be seen from Figure 2(B) that the spontaneous increase in A−1 associated with erythritol uptake in Ucp1KO mitochondria (trace b relative to trace d) was lower than in wild-type mitochondria (trace a relative to trace c). This confirms that the relationship between A−1 per mole of solute uptake was different in the two mitochondrial populations, which potentially accounts for the apparent decrease in the mPTP-dependent rates observed in Ucp1KO mitochondria (cf. Figure 2A). By expressing Ca2+-induced rates as a function of erythritol-induced rates, mPTP activity in both types of mitochondria can be compared in the same units of solute influx.
Figure 3 shows the average rates of Ca2+-induced swelling of wild-type and Ucp1KO mitochondria in the absence or presence of GDP or cyclosporin A. When correctly normalized to erythritol-induced rates, there was no effect of UCP1 ablation on Ca2+-induced solute flux in the presence or absence of the UCP1 inhibitor GDP, suggesting that UCP1 is not involved in mPTP formation (Figure 3A). Note that UCP1-dependent mPTP formation in these results was not masked by compensatory changes in ANT concentration, as both mitochondrial types contain similar amounts of ANT as assayed by Western-blot analysis (results not shown). GDP inhibited mPTP formation by ~50% (Figures 3A and 3B). This presumably occurs via an interaction with ANT, similar to the inhibitory effects of adenine nucleotides on mPTP , which is not without precedent as GDP has been shown to inhibit ANT-mediated proton conductance . Intriguingly, the cyclosporin-sensitive fraction of mPTP activity was significantly higher in the absence of UCP1 (~80% inhibited by cyclosporin, compared with ~60% in the presence of UCP1, Figures 3A and 3B). This could reflect a stress response that increases mPTP components, or their sensitivity to Ca2+, indirectly related to the absence of UCP1 or it could reflect a minor role of UCP1 in cyclosporin A-insensitive mPTP formation. If either explanation were true, however, why a similar amplitude difference was not seen in the absence of cyclosporin A is not clear (Figure 3A). Alternatively, it may indicate changes in factors that influence cyclosporin efficacy. An increased concentration of endogenous phosphate associated with the loss of UCP1 could be one possibility, assuming that phosphate does indeed influence cyclosporin inhibition of mPTP in BAT mitochondria. Most importantly, these results show that Ca2+-induced solute uptake activity, as well as the fraction of activity sensitive to cyclosporin A, was not lowered by UCP1 ablation, ruling out a structural role of UCP1 in the cyclosporin A-sensitive mPTP.
Calcium-induced mPTP formation in BAT mitochondria from wild-type and
ANT is proposed to play a primary role in the formation of mPTP. However, Kokoszka et al.  have demonstrated that mouse liver mitochondria in which ANT has been ablated still undergo cyclosporin A-sensitive permeability transition, albeit requiring higher calcium loads to do so. One interpretation of this finding is that other less abundant mitochondrial carrier proteins contribute to mPTP formation in the absence of ANT, reflecting a general role of this protein family in mPTP formation (e.g. ). In the present study, we developed a simple quantitative assay to study mPTP formation in mitochondria from wild-type and Ucp1KO mice. Our results demonstrate that UCP1 does not facilitate the cyclosporin A-sensitive mPTP, indicating that a role in mPTP formation is not a general characteristic of the mitochondrial carrier protein family. There is strong evidence that ANT is a functional component of the mPTP, rather than just influencing pore activity. In particular, several studies have shown that mPTP-like activity can be achieved following reconstitution of purified ANT into lipid bilayers [14,16,17]. In view of our conclusions, a likely explanation of the finding of Kokoszka et al.  is that, in addition to ANT, only specific members of the mitochondrial carrier family are involved in mPTP formation. This may be restricted to carriers that are more widespread across various tissues. A particularly strong candidate is the mitochondrial phosphate carrier. This carrier has recently been shown to bind cyclophilin D, similarly to ANT, in affinity-column and co-immunoprecipitation studies and may, therefore, contribute to cyclosporin A-sensitive mPTP in the absence of ANT [34,35].
In summary, we have developed a simple quantitative assay of mPTP formation in BAT mitochondria and demonstrated that UCP1 does not partake in cyclosporin A-sensitive mPTP formation. This finding is of significant importance as it eliminates a popular hypothesis that a role in cyclosporin A-sensitive mPTP formation is a general feature of the mitochondrial carrier protein family.
We thank Professor Barbara Cannon (The Wenner-Gren Institute, Stockholm University, Stockholm, Sweden) for providing Ucp1KO mice and Julie Buckingham for technical assistance.
This work was supported by the Medical Research Council; and by the Wellcome Trust [grant numbers 065326/Z/01/Z and 066750/B/01/Z].
Present address: Department of Cell and Developmental Biology, University College London, Gower Street, London WC1E 6BT, U.K.
Present address: Buck Institute for Age Research, Novato, CA 94945, U.S.A.