Downregulation of Adipose Glutathione S-Transferase A4 Leads to Increased Protein Carbonylation, Oxidative Stress, and Mitochondrial Dysfunction

C57BL/6J mice were placed on a normal chow (∼4% fat by weight; Teklad) or a high-fat (∼35% fat by weight, F3282; BioServ) diet at weaning (17). Mice were housed on a 12-h light/dark cycle and fed ad libitum with continual access to water. At 12–16 weeks of age, mice were killed by cervical dislocation, and tissues were harvested, frozen in liquid nitrogen, and stored at −80°C until further processing. Primary adipocytes were isolated from fresh epididymal fat pads as described previously (18). Mixed-strain mice B6;129S5-GSTa4^{Gt(neo) 619 Lex} were purchased from the Mutant Mouse Regional Resource Centers (University of California-Davis, Davis, CA). GSTA4 heterozygous mice were outbred to C57/BL6J mice, and the resulting heterozygous progenies were interbred to generate GSTA4-null and wild-type mice. The University of Minnesota Institutional Animal Care and Use Committee approved all experiments.

The 3T3-L1 fibroblasts were transduced with lentivirus carrying short hairpin RNA (shRNA) as described previously (19). shRNA sequences directed toward GSTA4 mRNA were purchased from Ambion. Each oligo and the reverse complement were synthesized and annealed, and the double-stranded DNA was ligated into pENTR/U6 cloning vector (Invitrogen) according to manufacturer's protocol. Cell lines used for experiments contained the following shRNA sequences: scrambled (Scr) control, AGTACTGCTTACGATACGGTGTGCTGTCCGTATCGTAAGCAGTACT; GSTAA4 knockdown, GGTATATAGATCCCAGGAGTGTGCTGTCCTCCTGGGATCTATATACC.

Protein carbonylation was detected using EZ-link Biotin Hydrazide (Pierce) as described previously (15), with slight modifications. Polyvinylidene fluoride membranes (MilliPore, Billerica, MA) were blocked in Odyssey Blocking Buffer (LI-COR, Lincoln, NE), and biotinylated proteins were detected with DyLight 800–conjugated streptavidin (Pierce, Rockford, IL) and visualized using an Odyssey Infrared Imager (LI-COR).

3T3-L1 adipocytes were scraped and incubated for 20 min on ice in 20 mmol/l Tris (pH 6.8) and 1 mmol/l EDTA containing protease inhibitors. Cells were lysed with 40 strokes of a Dounce homogenizer, and the resulting homogenate was supplemented with a final concentration of 220 mmol/l mannitol and 70 mmol/l sucrose. For mitochondrial isolation from adipose tissue, epididymal fat pads were minced, washed in ice-cold Krebs-Ringer HEPES, and lysed with 1:5 wt/vol of isolation buffer (20 mmol/l Tris-HCl, 220 mmol/l mannitol, 70 mmol/l sucrose, 1 mmol/l EDTA, pH 7.4, supplemented with protease inhibitors) by Dounce homogenization. Homogenates were centrifuged at 700g to remove nuclei, unbroken cells, and the lipid cake. Mitochondria were recovered by centrifugation at 12,000g.

Oxidative respiration was assessed in isolated mitochondria as described previously (20) using a FOXY-R Oxygen Sensor (Ocean Optics, Dunedin, FL). Isolated mitochondria were incubated at room temperature in 10 mmol/l HEPES (pH 7.4), 125 mmol/l KCl, 5 mmol/l MgCl₂, and 2 mmol/l K₂HPO₄ supplemented with 5 mmol/l pyruvate and 5 mmol/l malate to stimulate state 2 respiration. State 3 respiration was measured after the addition of 0.5 mmol/l ADP, and oxygen consumption rate was normalized to mitochondrial protein. TPP-HE was used to detect superoxide in isolated mitochondria as described previously (21).

Microarray analysis of human genes expressed in omental and subcutaneous adipose tissue was reported by MacLaren et al. (22). Dataset analysis was conducted using the Significant Analysis of Microarrays procedure (23) version 3.02 available at http://www-stat.stanford.edu/∼tibs/SAM. Statistical analyses were conducted using the statistical package SAS, version 9.1.3 (SAS Institute, Cary, NC).

All values are expressed as mean ± SEM. Statistical significance was determined using the two-tailed Student t test assuming unequal variances or, where appropriate, a two-way ANOVA with Bonferroni or Holm-Sidak post hoc analysis. P values < 0.05 are considered significant (*) with an increased significance of P value < 0.01 indicated (**).

To evaluate the expression of genes linked to oxidative stress and 4-HNE metabolism, quantitative RT-PCR (qPCR) (supplementary Table 1, available in an online appendix at http://diabetes.diabetesjournals.org/cgi/content/full/db09-1105/DC1) was performed on mRNA isolated from gonadal white adipose tissue of lean or obese male C57BL/6J mice (Fig. 1,A). Adipose tissue from obese animals exhibited increased expression of p40 phox subunit of NADPH oxidase and heme oxygenase (HO-1) and trends toward increased expression of superoxide dismutase 1 (SOD-1), glutathione peroxidase 1 (GPX-1), and peroxyredoxin 1 (PRDX-1), all consistent with an antioxidant stress response (2). In contrast, the expression of multiple isoforms of the GST family (A4, A3, M2) was decreased in obese mice compared with lean controls. Most notably, the expression of GSTA4 decreased approximately threefold to fourfold, consistent with microarray analysis of lean and obese C57BL/6J mice in which GSTA4 expression was profiled among the most highly regulated transcripts (24). The expression of other 4-HNE metabolizing enzymes including several aldehyde dehydrogenases (ALDH1A 1/7, ALDH2, and FALDH) was not significantly altered with obesity (Fig. 1,A). GSTA3 and GSTA4 expression was also decreased in obese female mice (Fig. 1,B) relative to lean controls. Interestingly, the basal GSTA4 expression in adipose tissue of lean female mice was approximately twofold greater than in lean male mice, such that obese female mice express GSTA4 at levels comparable with that expressed by lean male animals (Fig. 1 B).

To determine the tissue specificity of GSTA4 downregulation, qPCR was performed on mRNA isolated from epididymal white adipose tissue (EWAT), subcutaneous white adipose tissue, brown adipose tissue, liver, and gastrocnemius muscle of lean and obese male mice (Fig. 1,C). Whereas decreased GSTA4 expression was observed in both visceral and subcutaneous white adipose tissue, no significant change was observed in other insulin-responsive tissues analyzed. Because adipose tissue contains multiple cell types, adipocytes were separated from stroma in EWAT by collagenase digestion and exhibited an ∼95% decrease in GSTA4 expression in the adipocyte fraction. Reduced expression of GSTA4 was not limited to high-fat–fed C57BL/6J mice. GSTA4 mRNA expression was also significantly decreased in adipose tissue from ob/ob animals (Fig. 1 D), and GSTA4 expression is downregulated ∼10-fold in adipose tissue of genetically obese BTBR mice (http://www.diabetes.wisc.edu; [25]), indicating that the expression of GSTA4 is markedly reduced in a variety of metabolic and genetic models of obesity and insulin resistance.

To investigate the mechanism underlying reduced GSTA4 expression in insulin-resistant adipocytes, we assessed GSTA4 mRNA expression in response to a variety of hormones and metabolites using the 3T3-L1 cell culture system. Treatment of 3T3-L1 adipocytes with the proinflammatory cytokine TNF-α resulted in a time- and concentration-dependent decrease in GSTA4 expression. After 24-h treatment, GSTA4 mRNA expression was reduced 40% with 100 pmol/l TNF-α and 80% with 1 nmol/l TNF-α (Fig. 2,A). No further reduction of GSTA4 expression was obtained with 10 nmol/l TNF-α (data not shown). The reduced GSTA4 expression was observed as early as 8 h with 1 nmol/l TNF-α treatment (Fig. 2 B).

To assess the expression of GSTA4 in human obesity and insulin resistance, we evaluated GSTA4 expression in omental and subcutaneous adipose from obese diabetic subjects and nondiabetic subjects and compared it with lean counterparts using microarray analysis (22). Interestingly, GSTA4 expression in adipose tissue of humans was decreased in the obese insulin-resistant population relative to lean and obese insulin-sensitive individuals (Fig. 3,A) and was verified using real-time PCR (results not shown). Moreover, the decrease in GSTA4 mRNA was evident in both the subcutaneous and omental fat depots. There was no correlation between GSTA4 expression and BMI (Fig. 3,B), but there was a statistically significant negative correlation between GSTA4 levels and homeostatic model assessment of insulin resistance (HOMA-IR) (Fig. 3 C). Evaluation of GSTA3 expression revealed no relationship to HOMA-IR or BMI (results not shown).

Because GSTA4 is central to 4-HNE detoxification and metabolism and carbonylation is increased with obesity (15,26), we evaluated whether decreased GSTA4 expression leads directly to increased protein carbonylation. To that end, 3T3-L1 fibroblasts were transduced with shRNA directed against GSTA4 mRNA or nonspecific scrambled control sequence to establish GSTA4 knockdown and Scr cell lines. Although several distinct shRNA sequences were analyzed for GSTA4 silencing, one line with ∼60–70% decrease in GSTA4, comparable with that observed in the animal system, was chosen for detailed assessment (Fig. 4,A); some measures were confirmed in other silenced cell lines. Although GSTA3 was not expressed in the preadipocytes at an appreciable level, its expression increased during preadipocyte differentiation (data not shown) and was upregulated approximately twofold in GSTA4 knockdown adipocytes compared with Scr adipocytes (Fig. 4 A).

GSTA4 knockdown 3T3-L1 cells differentiated normally and expressed adipocyte marker proteins peroxisome proliferator–activated receptor-γ (PPARγ), CCAAT/enhancer binding protein α (CEBPα), adipocyte fatty acid–binding protein (A-FABP/aP2), β-actin, and lipoprotein lipase (LPL) to the same extent as Scr cells. Interestingly, expression of the fatty acid translocase CD36 was upregulated approximately twofold in the GSTA4 knockdown adipocytes (Figs. 4 B).

Protein carbonylation in GSTA4 knockdown and Scr control cells was assessed by biotin hydrazide modification (Fig. 4 C) (15). Adipocytes exhibited an approximately threefold to fourfold increase (P < 0.01) in total protein carbonylation relative to preadipocytes for both GSTA4 knockdown and Scr cell lines (n = 4). Increased carbonylation of specific proteins was noted in GSTA4 knockdown relative to Scr control adipocytes. The prominent band near ∼15 kDa in adipocytes has previously been identified as the adipocyte fatty acid–binding protein (aP2) (15). Another protein at ∼145 kDa (**) exhibited an approximately twofold to threefold increase (P < 0.01) in carbonylation in the GSTA4 knockdown cells. This band was excised from the gel and digested with trypsin, and the peptides were sequenced by liquid chromatography–electrospray ionization tandem mass spectrometry. The resultant peptides (nine unique peptides representing 8% sequence coverage) identified the protein as xanthine dehydrogenase (supplementary Table 2).

To determine the influence of increased protein carbonylation on adipocyte function, we examined a variety of metabolic parameters linked to glucose and lipid metabolism. GSTA4 knockdown adipocytes exhibited a significant increase in basal glucose transport, resulting in a net decrease in insulin-stimulated hexose uptake (Fig. 5,A and B). Western analysis indicated increased expression of the basal GLUT, GLUT1 (Fig. 5,C), but not the insulin-responsive GLUT, GLUT4. Consistent with increased hexose metabolism, analysis of reduced coenzyme levels revealed that the ratio of NAD⁺/NADH was significantly lower in GSTA4 knockdown cells (Fig. 5,D) and the culture medium of GSTA4 knockdown cells was slightly acidic (results not shown) due to a 65–70% increased level of L(+)-lactate compared with scrambled control cells (Fig. 5 E).

Because tricarboxylic acid cycle (TCA) enzymes are targets of protein carbonylation and are inactivated by the addition of 4-HNE (27,28), GSTA4 knockdown and Scr adipocytes were assayed for small organic acids by direct injection tandem mass spectrometry (29). GSTA4 knockdown adipocytes had significantly increased (P < 0.01) levels of intracellular lactate, pyruvate, succinate, and citrate (Fig. 5 F). The ratio of lactate to pyruvate was also significantly decreased in GSTA4 knockdown adipocytes relative to Scr control cells, and in sum suggested that multiple steps in the tricarboxylic acid cycle may be compromised because of silencing of GSTA4 and increased protein carbonylation.

To profile lipid metabolism in GSTA4-silenced 3T3-L1 adipocytes, we evaluated ¹⁴C-acetate incorporation into lipid pools as a measure of de novo lipogenesis. GSTA4 knockdown adipocytes exhibited no difference in de novo lipogenesis under basal or insulin-stimulated conditions relative to scrambled control cells (results not shown). However, consistent with elevated CD36 expression (Fig. 4,B), fatty acid uptake measured by ³H-palmitate influx was slightly, but significantly, increased under basal (but not insulin-stimulated) conditions in GSTA4 knockdown adipocytes (results not shown). Although both basal glucose and fatty acid transport are increased in GSTA4 knockdown cells, total lipid storage was unchanged. We therefore analyzed lipolysis of nonesterified fatty acids from GSTA4 knockdown and Scr adipocytes. Silencing GSTA4 led to an ∼50% increase in basal lipolysis, even in the presence of insulin (Fig. 5,G). Insulin suppression of forskolin-stimulated lipolysis was slightly blunted in GSTA4 knockdown adipocytes (Fig. 5 H). These results were confirmed in separate GSTA4 knockdown 3T3-L1 cell lines generated from different shRNA sequences (data not shown).

To assess mitochondrial β-oxidation, the conversion of radiolabeled palmitate to CO₂ and soluble metabolites was evaluated (30). GSTA4 knockdown adipocytes exhibited decreased oxidation of [1-¹⁴C]-palmitate as determined by the production of ¹⁴C-labeled CO₂ (complete oxidation) and ¹⁴C-labeled acid-soluble metabolites (incomplete oxidation) (Fig. 5 I). Mass spectrometry–based analyses were used to detect changes in the acyl-carnitine profile of GSTA4-silenced adipocytes (supplementary Fig. 1) and revealed that acetyl-carnitine (C2) and several other long-chain acyl-carnitine species were elevated in GSTA4 knockdown cells.

Given the altered glucose metabolism and TCA cycle intermediates, we assessed mitochondrial respiration in GSTA4 knockdown and control cells. Mitochondria were isolated from GSTA4 knockdown and Scr adipocytes, and oxygen consumption was evaluated. GSTA4 silencing had a significant effect (P = 0.017) on oxygen consumption rate as assessed by two-way ANOVA with Bonferroni post hoc analysis. Whereas control 3T3-L1 adipocytes exhibited robust state 2 respiration and an increase in state 3 respiration after addition of ADP, GSTA4 knockdown mitochondria displayed approximately twofold decrease in state 2 respiration and no increase in oxygen consumption after addition of ADP (Fig. 6,A–C). As mitochondrial dysfunction is often coupled with increased reactive oxygen species generation, we evaluated superoxide anion production in isolated mitochondria (21). Silencing GSTA4 resulted in an approximately threefold increase in superoxide production in the mitochondrial matrix (Fig. 6 D). However, whole-cell ROS evaluated by the fluorescent probe chloromethyl 2′,7′-dichlorodihydrofluorescein diacetate (H₂DCFDA) was not changed in GSTA4 knockdown compared with Scr control cells (data not shown), suggesting that increased oxidative stress is centered on the mitochondrion and not a property of the entire cell.

In the muscle, insulin resistance is characterized by not only loss of mitochondrial function but also mitochondria protein and DNA, leading to reduced levels of functional organelles (31,32). As such, we evaluated markers of mitochondrial biogenesis at the mRNA, protein, and DNA level. The expression of the key transcription factors Nrf1 and Tfam as well as the central cofactor peroxisome proliferator–activated γ coactivator-1α (PGC-1α) are all reduced in GSTA4-silenced adipocytes as well as the expression of mitochondrial proteins cyclooxygenase IV (COX IV) and cytochrome c (Fig. 7,A and B). Interestingly, expression of manganese SOD (Mn-SOD) and uncoupling protein 2 (UCP2) was not affected by GSTA4 silencing. In the GSTA4 knockdown cells, endothelial NO synthase (eNOS) expression was downregulated ∼50%, suggesting that increased protein carbonylation initiates a cascade of events that links to the entire mitochondrial biogenesis pathway (32). Consistent with this, the abundance of the COX II and cytochrome b (mitochondrial) genes relative to UCP2 (nuclear) gene was significantly reduced (Fig. 7,C). Paralleling the reduction in state 3 respiration, Fig. 7 D shows that the activity of ATP synthase was reduced 50% in the GSTA4-silenced adipocytes.

To determine whether mitochondrial dysfunction in the GSTA4-silenced 3T3-L1 cells was also exhibited in animal systems, respiration was evaluated in mitochondria isolated from male GSTA4-null (−/−) mice and wild-type (+/+) littermates maintained on standard chow (lean) or high-fat (obese) diet. Lean or obese GSTA4-null mice exhibited no significant difference in body weight relative to wild-type controls (34.2 ± 3.3 g vs. 38.6 ± 4.0, chow diet; 45.6 ± 6.9 and 49.2 ± 9.0, high-fat diet). No changes in fasting glucose or insulin levels were found between wild-type and GSTA4-null mice (supplementary Fig. 2B). Figure 8 A and B show that in wild-type C57BL/6J mice, the lean to obese transition results in little change in state 2 respiration but a decrease in state 3 respiration, coincident with the downregulation of GSTA4. Interestingly, GSTA4-null mice exhibited a trend toward increased state 2 respiration relative to wild-type animals. The state 3 oxygen consumption rate of mitochondria from lean GSTA4-null mice was comparable with wild type; however, similar to mitochondria from GSTA4-silenced adipocytes, mitochondria from obese GSTA4-null mice displayed no increase in oxygen consumption in response to ADP.

Accompanying the changes in respiration, adipocyte mitochondria from wild-type mice produced twofold to threefold more matrix superoxide in the obese state compared with lean controls. Adipocyte mitochondria from GSTA4-null mice exhibited markedly increased matrix superoxide in the lean state compared with wild-type controls and an even greater level of superoxide in the obese state (Fig. 8,C). These findings are consistent with published reports that defects in oxidative phosphorylation lead to increased matrix superoxide (33) and are likely a consequence of elevated protein carbonylation in the mitochondria of EWAT from GSTA4-null mice (Fig. 8 D). Unlike the GSTA3 upregulation in GSTA4 knockdown 3T3-L1 cell culture model, there was no significant change in expression of GSTA3 or other glutathione S-transferases or dehydrogenases linked to 4-HNE metabolism in the GSTA4-null mice (supplementary Fig. 2A).

The work described here profiles the systemic metabolic events associated with downregulation of GSTA4 that initiate with carbonylation of cellular proteins. Protein carbonylation is a chemical event with multiple protein targets alkylated under conditions of increased oxidative stress, and the biological outcomes in a cell or tissue are not likely to be based solely on one specific protein modification event (34). As such, a systems-wide approach is needed to characterize functional consequences of carbonylation. Our previous work characterized carbonylated polypeptides in adipose tissue using proteomic methods (15), and this report extends those findings to metabolic outcomes. The results presented identify GSTA4 as a key determinant of adipocyte protein carbonylation and mitochondrial function and suggest that its activity may be a protective factor against metabolic dysfunction.

In humans, GSTA4 is downregulated in omental and subcutaneous depots of obese, insulin-resistant but not obese, insulin-sensitive individuals (Fig. 3). Similarly, GSTA4 is downregulated specifically in adipose tissue from obese, insulin-resistant C57BL/6J mice (15,24), in ob/ob animals (Fig. 1,D), or in TNF-α–treated 3T3-L1 adipocytes (Fig. 2). Previous work by Awasthi et al. (11) and Engle et al. (35) has shown GSTA4-null mice have increased levels of 4-HNE, reduced antioxidant capacity, and increased apoptosis. Although GSTA4 expression was downregulated in obese female mice, its basal expression was more robust than in males (Fig. 1 B), raising the possibility that increased levels of GSTA4 protect female mice from the harmful effects of lipid peroxidation products and may contribute to the attenuated insulin resistance characteristics observed in female C57BL/6J mice (36).

Although silencing GSTA4 in adipocytes also led to overall increased protein carbonylation, one protein target identified was xanthine dehydrogenase (Fig. 3 D). In vitro, xanthine dehydrogenase is converted from its dehydrogenase form to its oxidoreductase form by modification of cysteine residues (37). Such modification of xanthine dehydrogenase by 4-HNE or other lipid aldehydes could lead to an increased oxidoreductase activity of the enzyme and the production of superoxide anion, amplifying oxidative stress signaling. Interestingly, xanthine dehydrogenase is known to be converted to xanthine oxidoreductase in response to mitochondrial damage in vivo (38), providing a link between mitochondrial dysfunction and oxidative stress.

Consistent with elevated lactate, the increased basal glucose transport by GSTA4 knockdown adipocytes could be a compensatory response to diminished mitochondrial function. In muscle cells, mitochondrial dysfunction has previously been linked to increased basal glucose transport (39), and obese human type 2 diabetic patients also exhibit increased basal 2-deoxyglucose transport in skeletal muscle cells (20,40). Increased GLUT1 expression in GSTA4 knockdown adipocytes (Fig. 5 C) is consistent with previous reports of increased glucose transport via GLUT1 during treatment of epithelial cells with inhibitors of mitochondrial oxidative phosphorylation (41) as well as reports of oxidative stress–induced increases in basal glucose transport in adipocytes (3). Increased basal glucose transport may provide sufficient ATP for metabolism and signaling because the levels of total and phospho–AMP-activated protein kinase were not altered in the GSTA4-silenced adipocytes (data not shown).

Insulin resistance is correlated with increased basal lipolysis (42), and GSTA4 knockdown adipocytes exhibited ∼50% increased basal lipolysis in the presence or absence of insulin (Fig. 5,G). Surprisingly, GSTA4 knockdown adipocytes had no change in total triglyceride accumulation (results not shown), potentially because of increased fatty acid uptake. Consistent with this, the expression of CD36 protein, a plasma membrane fatty acid transporter whose expression is induced by the 4-HNE–responsive transcription factor Nrf2 (43), was significantly increased in the GSTA4 knockdown adipocytes (Fig. 4 B).

The increase in key organic anion intermediates suggests that the flux through the tricarboxylic acid cycle is attenuated. Previous proteomic data have identified multiple TCA cycle enzymes as well as complexes I–IV of the oxidative phosphorylation machinery as targets of carbonylation (34). The decrease in [1-¹⁴C]-palmitate oxidation (Fig. 5 I) indicates that multiple steps in lipid oxidation and/or metabolism of acetyl-CoA are reduced in the GSTA4-silenced cells. This is supported by mass spectrometry data that show elevated levels of several acyl-carnitine species (supplementary Fig. 1), and increased acetyl-carnitine suggests that acetyl-CoA is accumulating. As such, increased protein carbonylation in the mitochondrion is likely to lead to decreased functions such as tricarboxylic acid cycle and fatty acid oxidation (27,44).

A major finding of this study is that respiration is markedly altered in GSTA4 knockdown adipocytes (Fig. 6) and in adipocytes of both lean and obese GSTA4-null mice (Fig. 8). In the cell culture system, silencing of GSTA4 led to diminished oxygen consumption (Fig. 6,C) and increased NADH levels (Fig. 5 D), suggesting electron transfer through the electron transport chain is impaired. Moreover, there was no increase in oxygen consumption in response to ADP in mitochondria from the GSTA4-silenced adipocytes. Consistent with this, the activity of ATP synthase was decreased ∼50% in the GSTA4-silenced adipocytes. These observations may be due to a combination of factors, including increased proton leakage across the inner mitochondrial membrane, carbonylation of complex V proteins affecting the ability to couple the proton gradient to ATP production, the carbonylation of the adenine nucleotide translocator, or carbonylation-dependent changes in the abundance of critical proteins linked to state 3 respiration. Indeed, under certain conditions 4-HNE can facilitate proton leak in other cell types through adenine nucleotide translocator or uncoupling proteins (45,46).

In the GSTA4-null adipocytes, changes in both state 2 and state 3 respiration were similar but not identical to the 3T3-L1 GSTA4 knockdown system. In the animal model, mitochondria from lean wild-type C57BL/6J mice exhibit robust state 2 respiration that increased with the addition of ADP. Obese C57BL/6J mice exhibited no change in state 2 respiration relative to lean counterparts but had attenuated ADP-coupled oxygen consumption, potentially due to the downregulation of GSTA4. In GSTA4-null animals, mitochondria from lean and obese mice exhibited a trend toward increased state 2 respiration compared with the wild-type animals, possibly due to increased proton leakage. Indeed, previous studies by Echtay et al. (45) have suggested that carbonylation of uncoupling proteins may, under certain circumstances, lead to increased proton leak, thereby providing for increased state 2 respiration. Similar to the GSTA4-silenced cells, mitochondria from obese GSTA4-null mice exhibited virtually no increase in respiration with ADP (Fig. 8 A and B).

Associated with downregulation of GSTA4 is decreased expression of eNOS, Nrf1, PGC-1α, and Tfam, critical regulators of mitochondrial biogenesis (Fig. 7). Indeed, GSTA4-silencing resulted in loss of mitochondrial DNA and decreased expression of COX II and cytochrome c. Work by Nisoli and colleagues has focused on eNOS as the key regulator of TNF-α action (32) and determined that if eNOS activity is lost from adipocytes, the entire program of mitochondrial activation and biogenesis is affected (47). These data suggest that downregulation of GSTA4 is upstream of eNOS regulation and may be mechanistically regulated by protein carbonylation.

In sum, the results presented here focus on the role of GSTA4 as an antioxidant enzyme responsible primarily for elimination of reactive electrophiles from adipocytes. The results here suggest a model whereby downregulation of GSTA4 by proinflammatory cytokines results in increased protein carbonylation, altered glucose and lipid metabolism, decreased mitochondrial β-oxidation, TCA cycle activity, electron transport, and respiration. Thus, protein carbonylation in white adipose tissue may provide a molecular mechanism linking increased oxidative stress to metabolic dysfunction associated with insulin resistance.

This work was supported by National Institutes of Health (NIH) Grant DK-084669 to D.A.B., the Minnesota Obesity Center (NIH Grant DK-050456), and NIH National Heart, Lung, and Blood Institute Training Grant T32 HL-07741 to P.A.G.

No potential conflicts of interest relevant to this article were reported.

We thank the members of the Bernlohr research group who provided helpful suggestions regarding this work. We also thank Erik Refsland of the Minnesota Obesity Center for lentivirus production, Dr. Jason Fowler for assistance with studies using TNF-α, Dr. Bruce Witthuhn of the University of Minnesota Center for Mass Spectrometry and Proteomics for assistance with mass spectrometry, Dr. Stephen Katz for help with statistical analysis, and the Minnesota Supercomputing Institute for support in data analysis.