A signalling role for 4-hydroxy-2-nonenal in regulation of mitochondrial uncoupling
2003; Springer Nature; Volume: 22; Issue: 16 Linguagem: Inglês
10.1093/emboj/cdg412
ISSN1460-2075
Autores Tópico(s)Muscle metabolism and nutrition
ResumoArticle15 August 2003free access A signalling role for 4-hydroxy-2-nonenal in regulation of mitochondrial uncoupling Karim S. Echtay Karim S. Echtay MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Telma C. Esteves Telma C. Esteves MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Julian L. Pakay Julian L. Pakay MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Mika B. Jekabsons Mika B. Jekabsons MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Present address: Buck Institute, 8001 Redwood Boulevard, Novato, CA, 94945 USA Search for more papers by this author Adrian J. Lambert Adrian J. Lambert MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Manuel Portero-Otín Manuel Portero-Otín Department of Basic Medical Sciences, Faculty of Medicine, Lleida University, Lleida, 25198 Spain Search for more papers by this author Reinald Pamplona Reinald Pamplona Department of Basic Medical Sciences, Faculty of Medicine, Lleida University, Lleida, 25198 Spain Search for more papers by this author Antonio J. Vidal-Puig Antonio J. Vidal-Puig Departments of Clinical Biochemistry and Medicine and Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK Search for more papers by this author Steven Wang Steven Wang Clore Laboratory, University of Buckingham, Buckingham, MK18 1EG UK Search for more papers by this author Stephen J. Roebuck Stephen J. Roebuck MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Martin D. Brand Corresponding Author Martin D. Brand MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Karim S. Echtay Karim S. Echtay MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Telma C. Esteves Telma C. Esteves MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Julian L. Pakay Julian L. Pakay MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Mika B. Jekabsons Mika B. Jekabsons MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Present address: Buck Institute, 8001 Redwood Boulevard, Novato, CA, 94945 USA Search for more papers by this author Adrian J. Lambert Adrian J. Lambert MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Manuel Portero-Otín Manuel Portero-Otín Department of Basic Medical Sciences, Faculty of Medicine, Lleida University, Lleida, 25198 Spain Search for more papers by this author Reinald Pamplona Reinald Pamplona Department of Basic Medical Sciences, Faculty of Medicine, Lleida University, Lleida, 25198 Spain Search for more papers by this author Antonio J. Vidal-Puig Antonio J. Vidal-Puig Departments of Clinical Biochemistry and Medicine and Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK Search for more papers by this author Steven Wang Steven Wang Clore Laboratory, University of Buckingham, Buckingham, MK18 1EG UK Search for more papers by this author Stephen J. Roebuck Stephen J. Roebuck MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Martin D. Brand Corresponding Author Martin D. Brand MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK Search for more papers by this author Author Information Karim S. Echtay1, Telma C. Esteves1, Julian L. Pakay1, Mika B. Jekabsons1,2, Adrian J. Lambert1, Manuel Portero-Otín3, Reinald Pamplona3, Antonio J. Vidal-Puig4, Steven Wang5, Stephen J. Roebuck1 and Martin D. Brand 1 1MRC Dunn Human Nutrition Unit, Hills Road, Cambridge, CB2 2XY UK 2Present address: Buck Institute, 8001 Redwood Boulevard, Novato, CA, 94945 USA 3Department of Basic Medical Sciences, Faculty of Medicine, Lleida University, Lleida, 25198 Spain 4Departments of Clinical Biochemistry and Medicine and Cambridge Institute for Medical Research, University of Cambridge, Cambridge, UK 5Clore Laboratory, University of Buckingham, Buckingham, MK18 1EG UK *Corresponding author. E-mail: [email protected] The EMBO Journal (2003)22:4103-4110https://doi.org/10.1093/emboj/cdg412 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info Oxidative stress and mitochondrial dysfunction are associated with disease and aging. Oxidative stress results from overproduction of reactive oxygen species (ROS), often leading to peroxidation of membrane phospholipids and production of reactive aldehydes, particularly 4-hydroxy-2-nonenal. Mild uncoupling of oxidative phosphorylation protects by decreasing mitochondrial ROS production. We find that hydroxynonenal and structurally related compounds (such as trans-retinoic acid, trans-retinal and other 2-alkenals) specifically induce uncoupling of mitochondria through the uncoupling proteins UCP1, UCP2 and UCP3 and the adenine nucleotide translocase (ANT). Hydroxynonenal-induced uncoupling was inhibited by potent inhibitors of ANT (carboxyatractylate and bongkrekate) and UCP (GDP). The GDP-sensitive proton conductance induced by hydroxynonenal correlated with tissue expression of UCPs, appeared in yeast mitochondria expressing UCP1 and was absent in skeletal muscle mitochondria from UCP3 knockout mice. The carboxyatractylate-sensitive hydroxynonenal stimulation correlated with ANT content in mitochondria from Drosophila melanogaster expressing different amounts of ANT. Our findings indicate that hydroxynonenal is not merely toxic, but may be a biological signal to induce uncoupling through UCPs and ANT and thus decrease mitochondrial ROS production. Introduction Mitochondria are the main intracellular producers of reactive oxygen species (ROS) in most cells and are also important targets for their harmful effects (Halliwell and Gutteridge, 1999). Mitochondrial oxidative damage may be a major factor in many human pathologies, including neurodegenerative diseases, ischaemia/reperfusion injury and inflammatory disorders (Esterbauer et al., 1991). Although there are several manifestations of oxidative damage to biological molecules, lipid peroxidation may be especially harmful (Esterbauer et al., 1991; Halliwell and Gutteridge, 1999). The polyunsaturated fatty acyl groups of membrane phospholipids are highly susceptible to peroxidation by oxygen radicals, and a self-propagating chain of free radical reactions produces various aldehydes, alkenals and hydroxyalkenals, such as malondialdehyde and 4-hydroxy-2-nonenal (HNE). Many of these products are cytotoxic, probably because of their reactivity toward proteins. Hydroxynonenal is thought to be one of the most reactive and an important mediator of free-radical damage (Esterbauer et al., 1991). Hydroxynonenal can chemically modify several amino acid residues of proteins: the sulphydryl group of cysteine, the imidazole moiety of histidine and the ϵ-amino group of lysine (Esterbauer et al., 1991; Uchida and Stadtman 1992; Nadkarni and Sayre 1995; Cohn et al., 1996). It has broad biological toxicity: inhibition of DNA and protein synthesis, inactivation of enzymes, modification of low density lipoprotein and modulation of gene expression (Esterbauer et al., 1991). Mitochondrial proteins are targets of hydroxynonenal adduct formation following oxidative stress in vivo and in vitro, and hydroxynonenal inactivates the 2-oxoglutarate dehydrogenase and pyruvate dehydrogenase complexes, cytochrome c oxidase and NADH-linked respiration in isolated mitochondria (Humphries and Szweda, 1998; Humphries et al., 1998; Musatov et al., 2002). Here we show a novel homeostatic role of hydroxynonenal: it induces mitochondrial uncoupling by specific and inhibitable interactions with the uncoupling proteins UCP1, UCP2 and UCP3, and with the adenine nucleotide translocase (ANT). These proteins are members of a large family of at least 35 anion carriers present in the mitochondrial inner membrane (Bouillaud et al., 2001). Mild uncoupling decreases mitochondrial production of ROS, which can subsequently cause hydroxynonenal production (Papa and Skulachev, 1997). This suggests a negative feedback loop in which hydroxynonenal signals damage by ROS and decreases ROS production through induction of uncoupling by UCPs and ANT. Results and discussion Figure 1 shows that HNE increased the proton conductance of isolated rat kidney mitochondria. Respiration driving the leak of protons across the membrane at any particular membrane potential was faster in the presence of hydroxynonenal than in its absence, resulting in a kinetic curve that was displaced upwards (see Cadenas et al., 2002; Echtay et al., 2002a,b). A strong effect was seen with 35 μM hydroxynonenal (Figure 1B), but the increase in proton conductance was also detected at 1 μM hydroxynonenal (Figure 1A). This was not simply due to non-specific damage to the membrane, since it was fully prevented by GDP or by carboxyatractylate (CAT) (Figure 1). Results discussed below show that this increase in proton conductance was mediated through UCP2 and ANT. Unlike superoxide-induced uncoupling (Echtay et al., 2002a), hydroxynonenal-induced uncoupling occurred in the presence of defatted bovine serum albumin (BSA), and did not require added fatty acids. Figure 1.Hydroxynonenal activation of proton conductance through UCP2 and ANT: effect of HNE on proton leak kinetics in rat kidney mitochondria. Proton leak kinetics were measured as described in Materials and methods: (A) without BSA in the presence of 1 μM HNE; (B) in the presence of BSA and 35 μM HNE. Squares, control; diamonds, HNE (+H); filled circles, HNE plus 500 μM GDP (+H+G); triangles, HNE plus 2.5 μM CAT (+H+C); crossed squares, HNE plus GDP and CAT (+H+G+C). Inserts show respiration rates driving proton leak at 150 mV for the same dataset. Data are means ± SEM of three independent experiments each performed in duplicate. *P <0.05 versus control. Download figure Download PowerPoint The structural requirements of hydroxynonenal for activation of proton conductance are explored in Figure 2. Trans-2-nonenal (Figure 2A) had the same effects as HNE, showing that the 4-hydroxyl was not required. Trans-2-nonenoic acid (Figure 2B) was also effective, showing that the aldehyde could be replaced by carboxyl. However, there was no effect of the saturated analogues nonanal and nonanoic acid (Figure 2C), which lack the double bond at carbon-2, indicating that this double bond is required. We suggest that the reactive 2-alkenal functional group modifies specific residues in the UCPs and ANT, leading to increased proton transport activity. Interestingly, cinnamic acid (Figure 2D), trans-retinoic acid (Figure 3A) and trans-retinal (Figure 3B), which all contain this functional group, also induced GDP- and carboxyatractylate-sensitive proton conductance. Figure 2.Hydroxynonenal activation of proton conductance through UCP2 and ANT: effects of compounds related to HNE on proton leak kinetics in rat kidney mitochondria. Proton leak kinetics were measured as described in Materials and methods in the presence of: (A) BSA and 35 μM trans-2-nonenal; (B) 35 μM trans-2-nonenoic acid; (C) 35 μM nonanoic acid (insert: BSA and 35 μM nonanal); (D) 50 μM cinnamic acid. Squares, control; diamonds, studied compound (+H); filled circles, compound plus 500 μM GDP (+H+G); triangles, compound plus 2.5 μM CAT (+H+C); crossed squares, compound plus GDP and CAT (+H+G+C). Inserts in (A), (B) and (D) show respiration rates driving proton leak at 150 mV for the same dataset. Data are means ± SEM of three independent experiments each performed in duplicate. *P <0.05 versus control. Download figure Download PowerPoint Figure 3.Hydroxynonenal activation of proton conductance through UCP2 and ANT: effects of retinoic acid and retinal on proton leak kinetics in rat kidney mitochondria. Proton leak kinetics were measured as described in Materials and methods in the presence of: (A) 5 μM trans-retinoic acid; (B) 5 μM trans-retinal. Squares, control; diamonds, studied compound (+H); filled circles, compound plus 500 μM GDP (+H+G); triangles, compound plus 2.5 μM CAT (+H+C); crossed squares, compound plus GDP and CAT (+H+G+C). Inserts show respiration rates driving proton leak at 150 mV for the same dataset. Data are means ± SEM of three independent experiments each performed in duplicate. *P <0.05 versus control. Download figure Download PowerPoint Is UCP2 involved in the activation of proton conductance by hydroxynonenal in kidney mitochondria? The mRNA for UCP2 is found in kidney (Zhang et al., 2001; Couplan et al., 2002) but the mRNA for UCP3 is not (Boss et al., 1997), while UCP1 is found only in brown adipose tissue (BAT), so UCP2 is the only candidate UCP in kidney mitochondria. Western blot evidence for the presence of UCP2 protein in rodent kidney mitochondria is ambiguous, because of poor antibody specificity (Pecqueur et al., 2001). Couplan et al. (2002) failed to detect UCP2 in kidney mitochondria, but careful examination of their western blots suggests that UCP2 is expressed there at low levels, since the intensity of the immunoreactive band at ∼30 kDa was diminished in kidney mitochondria from ucp2−/− mice. Evidence for UCP2 in kidney mitochondria is stronger using functional tests. Purine nucleotides bind to UCP2 (Echtay et al., 2001; Jekabsons et al., 2002). They also inhibit superoxide-inducible proton conductance through UCP1 in BAT mitochondria and UCP3 in skeletal muscle mitochondria (Echtay et al., 2002a), and sensitivity to GDP appears to be diagnostic of UCP involvement in mitochondrial proton conductance. GDP inhibits superoxide-inducible proton conductance in kidney mitochondria (Echtay et al., 2002a), strongly suggesting that UCP2 is present in these mitochondria. Hydroxynonenal-inducible proton conductance in kidney mitochondria was sensitive to GDP (Figure 1), suggesting that activation by hydroxynonenal is mediated by UCP2. Figure 4A and B shows that although hydroxynonenal stimulated proton conductance in mitochondria from liver and heart, tissues that lack UCPs (Pecqueur et al., 2001; Echtay et al., 2002a), GDP was not inhibitory, consistent with the absence of UCP2 in these tissues. Figure 4.Effect of hydroxynonenal on mitochondrial proton conductance through ANT. Proton leak kinetics in mitochondria from (A) liver and (B) heart were measured as described in Materials and methods in the presence of BSA. Squares, control; diamonds, plus 35 μM HNE (+H); filled circles, HNE plus 500 μM GDP (+H+G); triangles, HNE plus 2.5 μM CAT (+H+C). Inserts show respiration rates driving proton leak at 150 mV for the same dataset. Data are means ± SEM of three independent experiments each performed in duplicate. *P <0.05 versus control. Download figure Download PowerPoint To explore whether UCP3 could also respond to hydroxynonenal, we examined the effect of hydroxy- nonenal on skeletal muscle mitochondria, which contain UCP3 but not UCP1 or UCP2 (Bouillaud et al., 2001; Pecqueur et al., 2001; Echtay et al., 2002a). Figure 5A shows that hydroxynonenal induced proton conductance in the absence, but not in the presence, of GDP. Confirmation of the role of UCP3 was obtained using skeletal muscle mitochondria from ucp3 knockout mice (Cadenas et al., 2002; Echtay et al., 2002a). Hydroxynonenal caused GDP-sensitive stimulation of proton conductance in skeletal muscle mitochondria from wild-type mice (Figure 5B), as it did in rats. However, hydroxynonenal stimulation of proton conductance was significantly less in ucp3 knockout compared with wild-type mitochondria, and GDP did not prevent this hydroxynonenal stimulation (Figure 5C). These results show that hydroxynonenal can uncouple skeletal muscle mitochondria through a GDP-sensitive interaction with UCP3. Figure 5.Hydroxynonenal activation of proton conductance through UCP3 and ANT. Proton leak kinetics were measured as described in Materials and methods in the presence of BSA in mitochondria from: (A) rat skeletal muscle; (B) skeletal muscle from wild-type mice; (C) skeletal muscle from ucp3−/− mice (Echtay et al., 2002a). Squares, control; diamonds, 35 μM HNE (+H); filled circles, HNE plus 500 μM GDP (+H+G); triangles, HNE plus 2.5 μM CAT (+H+C). Inserts show respiration rates driving proton leak at 150 mV for the same dataset. Data are means ± SEM of three independent experiments each performed in duplicate. *P <0.05 versus control. Download figure Download PowerPoint To determine whether UCP1 is also activated by hydroxynonenal, we examined mitochondria from warm-adapted rat BAT, which (unlike mitochondria from cold-adapted rats) contain sufficiently low amounts of UCP1 to permit coupling in the absence of added nucleotides (Echtay et al., 2002a). Figure 6 shows that GDP inhibited the endogenous UCP1 activity, lowering the control proton conductance to the basal level. Hydroxynonenal increased proton conductance substantially in the control without GDP, but stimulated it very little above basal in the presence of GDP (Figure 6), suggesting that uncoupling by UCP1 is also activated by hydroxynonenal. However, UCP2 and UCP3 mRNA (but not UCP2 protein) are also present in BAT (Ricquier and Bouillaud, 2000; Pecqueur et al., 2001), possibly weakening this conclusion. Confirmation of the role of UCP1 was obtained using yeast mitochondria expressing mouse UCP1 (Stuart et al., 2001; Echtay et al., 2002a). Mitochondria from control yeast containing empty vector showed little uncoupling by hydroxynonenal, and no effect of GDP (Figure 7A) (so yeast ANT, unlike the mammalian protein, is insensitive to HNE at the concentration used). In contrast, hydroxynonenal markedly stimulated the proton conductance of mitochondria from yeast expressing UCP1, and this stimulation was prevented by GDP (Figure 7B). These results clearly show that hydroxy nonenal increases GDP-sensitive proton conductance through UCP1. There is abundant evidence in the literature that UCP1 activation in BAT mitochondria causes stimulation of respiration by altering proton conductance, and not by causing slip of the proton pumps in the electron transport chain. The hydroxynonenal activation of respiration in UCP1-containing (but not control) yeast mitochondria and the lack of GDP-sensitive hydroxynonenal activation in UCP3 knockout mouse mitochondria show that hydroxynonenal alters the relationship between respiration rate and membrane potential by increasing proton conductance through the UCPs, and not by stimulating slip in electron transport. Figure 6.Hydroxynonenal activation of proton conductance through UCP1 and ANT in BAT mitochondria. Proton leak kinetics were measured as described in Materials and methods in the presence of BSA (1%) in mitochondria from warm-adapted rat BAT. (A) Leak kinetics: squares, control; filled squares, control plus 500 μM GDP (+G); diamonds, 50 μM HNE (+H); filled circles, HNE plus 500 μM GDP (+H+G); triangles, HNE plus 2.5 μM CAT (+H+C); crossed squares, HNE plus GDP and CAT (+H+G+C). (B) Respiration rates driving proton leak at 150 mV for the same dataset. Data are means ± SEM of three independent experiments each performed in duplicate. *P <0.05 versus control; **P <0.05 versus +H. Download figure Download PowerPoint Figure 7.Hydroxynonenal activation of proton conductance through mouse UCP1 expressed in yeast mitochondria. Proton leak kinetics were measured as described in Materials and methods in mitochondria from: (A) yeast containing control empty vector; (B) yeast expressing mouse UCP1. Respiration rates driving proton leak were interpolated from the leak kinetics at 82 mV. Data are means ± SEM of three independent experiments each performed in duplicate. * P <0.05 versus control. Download figure Download PowerPoint Taken together, the results discussed above show that UCP1, UCP2 and UCP3 can each catalyse hydroxy nonenal-induced GDP-sensitive proton conductance. However, it was also clear that a component of the hydroxynonenal effect persisted in mitochondria lacking UCPs (Figures 4A and B, and 5C). Stimulation by hydroxynonenal was not prevented by glybenclamide, a KATP channel blocker, or cyclosporin A, an inhibitor of the mitochondrial permeability transition (Figure 8). It was insensitive to superoxide dismutase, required ∼2 min reaction time and was not fully reversible, since GDP (or carboxyatractylate) added after hydroxynonenal was only partially inhibitory. Figure 8.Hydroxynonenal activation of proton leak. Mitochondria from rat liver, kidney, and skeletal muscle were incubated as described in Materials and methods in the presence of BSA. 35 μM HNE, 500 μM GDP, 2.5 μM CAT, 1 μM cyclosporin A (CSA), 1 μM glybenclamide (GC) and 12 U.ml−1 superoxide dismutase (SOD) were present where indicated. Respiration rates driving proton leak were interpolated from the leak kinetics at 150 mV. Data are means ± SEM of three independent experiments each performed in duplicate. *P <0.05 versus control. Download figure Download PowerPoint The ubiquitous ANT is a fourth target for hydroxy nonenal. Carboxyatractylate (CAT) (Figures 1, 4 and 5) and bongkrekate (BKA) (Figure 9), potent and highly specific inhibitors of ANT (Klingenberg, 1975), strongly inhibited uncoupling induced by hydroxynonenal in mitochondria from kidney, liver, heart and skeletal muscle. ANT is present in BAT mitochondria at about the same concentration as it is in liver mitochondria (Chavez et al., 1996), and in BAT mitochondria (Figure 6) carboxyatractylate inhibited hydroxynonenal-induced uncoupling by about the same absolute extent as it did in liver mitochondria (Figure 4A). However, because of the high UCP1 concentration in BAT mitochondria, the percentage inhibition by carboxyatractylate was much less than it was in mitochondria from the other tissues. Confirmation of the role of ANT was obtained using mitochondria from Drosophila melanogaster expressing different amounts of ANT (M.D.Brand, unpublished observation), where hydroxynonenal stimulation correlated well with ANT content (Figure 10). This stimulation in Drosophila was completely sensitive to carboxyatractylate and insensitive to GDP (not shown), confirming that ANT catalyses hydroxynonenal-induced proton conductance. The effect of varying ANT was not due to non-specific damage to the membrane as a result of overexpression of a mitochondrial protein, since the extra HNE activation was still fully sensitive to CAT. Figure 9.Hydroxynonenal activation of proton conductance through ANT: effect of BKA. Mitochondria from different rat tissues were incubated as described in Materials and methods without BSA. (A) Kidney; (B) liver; (C) heart; (D) skeletal muscle. Squares, control; diamonds, plus 35 μM HNE; filled circles, HNE plus 8 μM BKA. Data are means ± SEM of three independent experiments each performed in duplicate. Download figure Download PowerPoint Figure 10.Dependence of hydroxynonenal activation on ANT content in Drosophila mitochondria. Proton leak was measured as described in Materials and methods with 2 mM MgCl2 and 0.3% (w/v) BSA present, at 25°C, using 10 mM glycerol 3-phosphate as substrate and titrating with cyanide up to ∼200 μM. The stimulation of respiration by 35 μM HNE was interpolated from the leak kinetics at the highest common potential (140 mV). ANT content was measured by titration with CAT. Circle, wild-type flies; triangle, sesB+/− flies (sesB codes for ANT; Zhang et al., 1999); square, flies with a 10.3 kb fragment containing sesB inserted into chromosome 2 or 4. Data are means ± SEM of six independent experiments each performed in duplicate. Download figure Download PowerPoint Despite the clear demonstration that hydroxynonenal can induce proton conductance through both UCPs and ANT, there were perplexing effects of GDP and carboxyatractylate: where both types of carrier were present, the inhibitors were not fully additive. Thus, in kidney (Figure 1) or skeletal muscle (Figure 5), either inhibitor alone was as effective as both together. This was not due to lack of specificity of the inhibitors, as there was no effect of carboxyatractylate on binding of fluorescently tagged GDP to UCP2 (Figure 11), and carboxyatractylate had only small percentage effects in BAT mitochondria, which have little ANT relative to UCP1 (Figure 6). Conversely, GDP had no effect in mitochondria lacking UCPs (Figures 4A and B, 5C). We speculate that hydroxynonenal traps ANT and UCP in a heterodimer that is sensitive to either inhibitor. Figure 11.Effect of CAT on nucleotide binding to UCP2. Fluorescence binding measurement of Mant-GDP to renatured UCP2 inclusion bodies was performed as described in Materials and methods. Diamonds, no CAT; squares, plus 1 μM CAT; triangles, plus 10 μM CAT. Download figure Download PowerPoint Retinoic acid is a powerful activator of ucp1 gene expression, working through nuclear receptors (Alvarez et al., 1995). It also directly activates proton transport through UCP1 and UCP2 (Rial et al., 1999). Our observations confirm that retinoic acid can activate GDP-sensitive proton transport (by UCP2) in kidney mitochondria, and show that it can also induce carboxy atractylate-sensitive proton conductance through ANT (Figure 3A). The carboxylic acid group of retinoic acid is not required, as retinal (in contrast to Rial et al., 1999) has the same effects (Figure 3B). Retinoic acid, retinal and the more potent analogue TTNPB (Rial et al., 1999) all contain the same 2-alkenal functional group as hydroxynonenal, so we propose that they too induce proton transport by modifying particular residues in UCPs and ANT, rather than acting as inert ligands. They may be more promising than the more toxic hydroxynonenal as lead compounds for the development of anti-obesity pharmaceuticals that work by specifically activating mitochondrial uncoupling by UCPs (Harper et al., 2001). Superoxide induces uncoupling through the UCPs (Echtay et al., 2002a). We investigated the hypothesis that superoxide, by initiating lipid peroxidation, releases hydroxynonenal as a second messenger that is the direct inducer of proton conductance by the UCPs (data not shown). There are differences between the two activators: the effect of superoxide requires added fatty acids and is insensitive to carboxyatractylate and specific for the UCPs (Echtay et al., 2002a), whereas hydroxynonenal does not require fatty acids and also targets ANT. Treatment of kidney mitochondria with superoxide exactly as in Echtay et al. (2002a) did not produce detectable amounts of hydroxynonenal using a commercial assay kit (Calbiochem). There was no change in the fatty acyl composition of the phospholipids, in the double bond and peroxidizability indices, or in five markers of different kinds of oxidative damage to proteins [assayed by GC/MS as described by Portero-Otín et al. (1999) and Brand et al. (2002)]. We also found that oxidized forms of arachidonic and linoleic acids, 8(S)-HETE (8S-hydroxy-5Z,9E,11Z, 14Z-eicosatetraenoic acid) and 9-HODE [(±)9-hydroxy-10E,12Z-octadecadienoic acid] had no effect on proton conductance. Thus, we have no evidence that hydroxynonenal (or another lipid peroxidation product) mediates activation of UCPs by superoxide. However, the amounts of hydroxynonenal involved might be too low to be detected by our assays. The effects of superoxide and hydroxynonenal were found to be non-additive, supporting the hypothesis that they activate the same process. Figure 12 shows that mitochondrial ROS production was sensitive to hydroxynonenal (see below). Figure 12.Hydroxynonenal decreases mitochondrial ROS production. H2O2 production by kidney mitochondria was measured as described in Materials and methods in the presence of 10 μM HNE and 500 μM GDP as indicated. Data are means ± range of two independent experiments each performed in duplicate. *P <0.05 versus control; **P <0.05 versus +HNE. Download figure Download PowerPoint Conclusion The results presented here show that physiologically relevant concentrations of HNE, a major product of oxidant-induced peroxidation of membrane phospholipids, specifically uncouple mitochondria. Structurally related compounds, such as trans-2-nonenal, trans-2-nonenoic acid, trans-retinoic acid, trans-retinal and other molecules containing the reactive 2-alkenal group have the same effect, suggesting that the alkenal group of these compounds reacts with a target protein in the mitochondria. Hydroxynonenal-induced uncoupling was inhibited by GDP, a potent inhibitor of uncoupling proteins UCP1, UCP2 and UCP3, and by CAT and BKA, potent inhibitors of the adenine nucleotide translocase. The GDP-sensitive proton conductance induced by hydroxynonenal was absent in skeletal muscle mitochondria from UCP3 knockout mice, appeared in yeast mitochondria expressing UCP1, and correlated with tissue expression of UCPs, demonstrating that it acted through the UCPs. The carboxyatractylate-sensitive hydroxynonenal stimulation of proton conductance correlated with adenine nucleotide translocase content in mitochondria from D.melanogaster expressing different amounts of the sesB gene product. This,
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