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Published online April 24, 2007
Diabetes 56:1751-1760, 2007
DOI: 10.2337/db06-1135
© 2007 by the American Diabetes Association
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Adipose Mitochondrial Biogenesis Is Suppressed in db/db and High-Fat Diet–Fed Mice and Improved by Rosiglitazone

James X. Rong1, Yang Qiu2,3, Michael K. Hansen3, Lei Zhu3,4, Vivian Zhang3, Mi Xie1, Yuji Okamoto5, Michael D. Mattie6, Hiroyuki Higashiyama5, Satoshi Asano5, Jay C. Strum6, and Terence E. Ryan3

1 High Throughput Biology, Discovery Research, GlaxoSmithKline, Research Triangle Park, North Carolina
2 Cheminformatics, Discovery Research, GlaxoSmithKline, Research Triangle Park, North Carolina
3 Integrative Biology, High Throughput Biology, Discovery Research, GlaxoSmithKline, King of Prussia, Pennsylvania
4 Biomedical Data Sciences, GlaxoSmithKline, Research Triangle Park, North Carolina
5 Tsukuba Research Laboratories, High Throughput Biology, Discovery Research, GlaxoSmithKline, Ibaraki, Japan
6 Department of Quantitative Expression, Genetics Research, GlaxoSmithKline, Research Triangle Park, North Carolina

Address correspondence and reprint requests to James X. Rong, High Throughput Biology, Discovery Research, GlaxoSmithKline, 5 Moore Dr., Research Triangle Park, NC. E-mail: james.x.rong{at}gsk.com

Abbreviations: BAT, brown adipose tissue; CIDEA, cell death–inducing DFFA-like effector a; CPT, carnitinepalmitoyl transferase; FAO, fatty acid oxidation; HSP, heat-shock protein; OXPHOS, oxidative phosphorylation; PGC, PPAR coactivator; PPAR, peroxisome proliferator–activated receptor; RIP, receptor interacting protein; RSG, rosiglitazone; TCA, tricarboxylic acid; UCP, uncoupling protein; WAT, white adipose tissue


   ABSTRACT
TOP
 ABSTRACT
RESEARCH DESIGN AND METHODS
 RESULTS
 DISCUSSION
 REFERENCES
 
The objective of this study was to further establish and confirm the relationship of adipose mitochondrial biogenesis in diabetes/obesity and the effects of rosiglitazone (RSG), a peroxisome proliferator–activated receptor (PPAR) {gamma} agonist, by systematically analyzing mitochondrial gene expression and function in two mouse models of obesity and type 2 diabetes. Using microarray technology, adipose mitochondrial gene transcription was studied in db/db, high-fat diet–fed C57BL/6 (HFD) and respective control mice with or without RSG treatment. The findings were extended using mitochondrial staining, DNA quantification, and measurements of citrate synthase activity. In db/db and HFD mice, gene transcripts associated with mitochondrial ATP production, energy uncoupling, mitochondrial ribosomal proteins, outer and inner membrane translocases, and mitochondrial heat-shock proteins were decreased in abundance, compared with db/+ and standard-fat diet–fed control mice, respectively. RSG dose-dependently increased these transcripts in both db/db and HFD mice and induced transcription of mitochondrial structural proteins and cellular antioxidant enzymes responsible for removal of reactive oxygen species generated by increased mitochondrial activity. Transcription factors, including PPAR coactivator (PGC)-1ß, PGC-1{alpha}, estrogen-related receptor {alpha}, and PPAR{alpha}, were suppressed in both models and induced by RSG. The effects of RSG on adipose mitochondrial genes were confirmed by quantitative RT-PCR and further supported by mitochondrial staining, mitochondrial DNA quantification, and citrate synthase activity. Adipose mitochondrial biogenesis was overwhelmingly suppressed in both mouse models of diabetes/obesity and globally induced by RSG. These findings suggest an important role of adipose mitochondria in diabetes/obesity and the potential for new treatment approaches targeting adipose mitochondria.

Peroxisome proliferator–activated receptor (PPAR){gamma} agonists, including rosiglitazone (RSG), are effective drugs for the treatment of type 2 diabetes. It is well established that RSG induces adipogenesis and causes body-wide lipid repartitioning by increasing adipose triglyceride content, thereby lowering free fatty acids, glycerol, triglycerides, and glucose in the circulation, which is associated with increased insulin sensitivity of the liver, muscle, and other organs. Critical to this process, adipose tissue, which highly expresses PPAR{gamma}, serves not only as a lipid storage depot but also as an endocrine organ producing adipokines that regulate the activity of other tissues (rev. in 1,2).

There has been growing interest in exploring the involvement of adipose mitochondria in the regulation of whole-body energy homeostasis (3–9). Recent studies suggest that diabetes/obesity is accompanied by a decrease in the expression of adipose mitochondrial genes in ob/ob mice (8) and impaired adipose mitochondria in db/db mice (9) and that the compromised mitochondrial conditions in ob/ob and db/db mice were reversible by RSG (8,9). Mitochondrial dysfunction in adipose tissue, like that in skeletal muscle (10,11), is linked to diabetes/obesity in humans (3).

Mitochondria produce >95% of cellular ATP, required by adipocytes for triglyceride synthesis and adipokine synthesis and secretion, in addition to other general cellular processes. Mitochondria also are indispensable in nonshivering thermogenesis, which takes place in brown adipose tissue (BAT) in small mammals and relies on energy uncoupling via short circuiting the proton gradient across the mitochondrial inner membrane (12,13). The relationship of adipose mitochondrial gene expression in diabetes/obesity has not been studied systematically in db/db or high-fat diet–fed (HFD) mice, two widely used models of type 2 diabetes and obesity. Whereas both models are characterized by high blood glucose and insulin levels, dyslipidemia, and obesity, different mechanisms underlie the disease. db/db mice carry a spontaneous mutation in the leptin receptor (14) and suffer severe glucose intolerance, hyperglycemia, and hyperinsulinemia. In contrast, HFD mice have milder glucose intolerance and other metabolic symptoms, which is reversible with a low-fat diet (15).

In this study, transcriptional profiling was conducted using microarray technology and focused on adipose mitochondrial gene expression in db/db and HFD mice and the effects of RSG treatment. The expression of genes regulating mitochondrial ATP production, energy uncoupling, mitochondrial structure, mitochondrial protein translation, transportation, and folding were examined, as was as the expression of transcription factors regulating mitochondrial biogenesis. The results indicate that both mouse models exhibit compromised mitochondrial biogenesis in adipose tissue, which is improved dose dependently by RSG. The transcriptional evidence was confirmed by quantitative real-time RT-PCR, mitochondrial staining, mitochondrial DNA content, and examination of citrate synthase activity. The findings support a new understanding of PPAR{gamma} actions in diabetes/obesity treatment.


   RESEARCH DESIGN AND METHODS
TOP
 ABSTRACT
 RESEARCH DESIGN AND METHODS
RESULTS
 DISCUSSION
 REFERENCES
 
Male, 4-week-old C57BL/6J and C57BL/Ks db/db and db/+ mice were obtained from The Jackson Laboratory (Bar Harbor, ME) and housed in a temperature- and humidity-controlled environment with a 12-h light/dark cycle. db/db and db/+ mice were fed a standard chow (Purina 5001; TestDiet, Richmond, IN) throughout the experiments. For the HFD model, 5-week-old C57BL/6J mice were placed on either a high-fat diet (D12331, 58% kcal from fat; Research Diets, New Brunswick, NJ) or a standard-fat diet (d12329, 11% kcal), with coconut oil as the main fat source, matching that in the high-fat diet (15). All animals were allowed free access to food and water. Care and use of the animals were in accordance with protocols approved by the GlaxoSmithKline Institutional Animal Care and Use Committee.

RSG administration.
RSG maleate (BRL49653C) was obtained from GlaxoSmithKline (Harlow, U.K.). For the HFD model, RSG treatment began after 8 weeks on either the high-fat or standard-fat diet. For the db/db model, treatment began in db/db and db/+ mice at 8 weeks of age. In both models, mice received RSG (1, 3, or 10 mg/kg) or vehicle (0.5% methylcellulose) by oral gavage twice daily for 14 days. Blood samples were taken on day 0 and 14 after 6-h fasting. Ten mice were used in each treatment group in each model.

Plasma measurements.
Plasma glucose and insulin was measured using an automated clinical chemistry analyzer (olympus au400; Olympus America, Melville, NY) and an enzyme-linked immunosorbent assay kit (ALPCO Diagnostics, Windham, NH), respectively. A1C levels were measured from whole blood using the Variant II (Bio-Rad; Hercules, CA).

Affymetrix microarray.
All adipose tissues used in the microarray experiment were inguinal subcutaneous adipose tissue. RNA isolation, DNase I treatment, reverse transcription and cRNA synthesis, labeling, and hybridization with Genechips mouse genome 430a array (Affymetrix Microarray Suite; Affymetrix, Santa Clara, CA) were conducted following the standard affymetrix protocol (online appendix [available at http://dx.doi.org/10.2337/db06-1135]). Total RNA (5 µg) from single animals was used for each chip. The RNA samples were randomized before cRNA synthesis and rerandomized before hybridization to avoid batch effects. Array intensity data were captured by the Genechip Computer Operating System using the algorithm (MAS 5.0; Affymetrix).

Immunohistochemistry and morphometric analysis.
Inguinal adipose tissue fixed in 10% neutral buffered formalin was paraffin embedded and sectioned (5 µm in thickness). After deparaffinization and antigen retrieval (16), the sections were stained with goat anti–cytochrome c (1:500 dilution; Santa Cruz), goat anti–mitochondrial heat shock protein 60 (HSP60) (1:200; Santa Cruz), or rabbit anti–uncoupling protein (UCP)-1 (1:2,000; Abcam, Cambridge, U.K) polyclonal antibodies (online appendix).

Quantification of cytochrome c–positive area was performed by two blinded pathologists using eCognition (Definiens, München, Germany), following manufacturer's instructions. Details of image acquisition and morphometric analysis were provided in the online appendix. Cytochrome c–positive area was calculated as cytochrome c–positive area divided by the total area of examined images and expressed as µm2/mm2. UCP-1–positive multilocular cells on acquired images were identified and counted by blinded pathologists and expressed as number of cells per 0.705 mm2.

Quantification of RNA and mitochodrial DNA by quantitative real-time PCR.
Transcriptomics results from the microarray analysis were confirmed using representative genes by quantitative RT-PCR (online appendix). Relative amounts of nuclear and mitochondrial DNA were determined by quantitative real-time PCR using glyceraldehydes-3-phosphate dehydrogenase and cytochrome b, respectively (17) (online appendix). The ratio of mitochondrial DNA to nuclear DNA reflects the tissue concentration of mitochondria per cell.

Citrate synthase activity in adipose tissue.
Citrate synthase activity was measured similarly to Bogacka et al. (3) using a Sigma kit (online appendix). Protein concentrations in the lysate were determined using a micro biochronic acid protein assay kit (Pierce, Rockford, IL). The citrate synthase activity was expressed as µmol · min–1 · g protein–1.

Statistical analyses.
Plasma measurements are presented as means ± SE and were analyzed using two-way repeated-measures ANOVA with a post hoc analysis using the Student Newman Keuls multiple comparison test. P < 0.05 was considered statistically significant.

Microarray analysis was based on 10 chips per treatment group (1 chip for each mouse), five groups in each mouse model. Probe sets with intensity values ≥22.1, which represented the 95 percentile of the built-in Affymetrix negative control probe sets for all the chips, were considered present. Probe set intensity values were log10 transformed and analyzed using both ANOVA and the false discovery rate (18). P < 0.01 from ANOVA was used to select genes with a significant change because, in our analyses, this criterion was found to be more stringent than that using an false discovery rate q <0.1 (10% false discovery rate), an acceptable false-positive rate in microarray literature (e.g., 19). In addition, a 1.2-fold cutoff for median fold changes, previously used by others (e.g., 20) and consistently generating reproducible results in our microarray experiments (M.K.H., Y.Q., J.X.R., personal communications), was used for further gene selection.

Cytochrome c–positive areas, UCP-1–positive cell numbers, relative mitochondrial DNA content, and citrate synthase activity are presented as means ± SE. Statistical analyses of the differences between vehicle- and rosiglitazone-treated db/db mice and between vehicle-treated db/+ and vehicle-treated db/db mice were conducted using one-way ANOVA followed by Dunnett test, using vehicle-treated db/db mice as the control, and Student's t test, respectively. P < 0.05 was considered statistically significant.


   RESULTS
TOP
 ABSTRACT
 RESEARCH DESIGN AND METHODS
 RESULTS
DISCUSSION
 REFERENCES
 
Plasma measurements in db/db and HFD mice.
db/db mice had significantly higher glucose, insulin, and A1C levels than db/+ mice (Table 1). Fourteen days of RSG treatment significantly decreased glucose and insulin levels at all three doses. A1C levels were reduced with significant changes occurring with the 3 and 10 mg/kg of RSG. RSG significantly increased body weight and inguinal adipose weight (data not shown).


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  		TABLE 1 Glucose, A1C, and insulin levels in the db/db model

 
HFD mice had significantly higher glucose, insulin, and A1C levels than standard-fat diet–fed mice (SFD) (Table 2), but the levels were generally lower than those in db/db mice. In HFD mice, only the highest dose of RSG (10 mg/kg) significantly decreased glucose after 14 days of treatment, but all RSG doses significantly decreased insulin levels. There were no significant reductions in A1C with RSG treatment in the HFD mice. Body weight and inguinal adipose weight were significantly increased in mice treated with 3 and 10 mg/kg RSG (data not shown).


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  		TABLE 2 Glucose, A1C, and insulin levels in the HFD model

 
Transcription of adipose mitochondrial proteins regulating ATP production was suppressed in db/db and HFD mice and induced by RSG.
Mitochondria host enzymes necessary for the tricarboxylic acid (TCA) cycle, fatty acid oxidation (FAO), and oxidative phosphorylation (OXPHOS) pathways, all of which contribute to ATP production. As listed in online appendix Table 1, of 22,626 probe sets (each identifying one gene transcript) on Affymetrix mouse chip 430A, 248 represent genes encoding proteins localized to mitochondria and related to OXPHOS/TCA/FAO, based on Affymetrix chip annotation and confirmed by Entrez Gene (http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?CMD = search&DB = gene).

Of 248 probe sets, 241 (97%) were called "present" in the inguinal adipose tissue, composed of BAT and white adipose tissue (WAT) (21). Figure 1 shows that the expression of the majority of the OXPHOS/TCA/FAO genes in the tissue was suppressed in db/db and HFD mice compared with those in db/+ and SFD mice, respectively. In a dose-dependent manner, RSG induced the expression of most of the OXPHOS/TCA/FAO genes in both db/db and HFD mice. At 10 mg/kg, RSG increased the expression of the majority of the genes to a level equivalent to or higher than that in db/+ and SFD mice. This suggests that RSG is capable of correcting the compromised adipose mitochondrial gene expression in db/db and HFD mice.


Figure 1
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  		FIG. 1. Transcriptional regulation of genes involved in mitochondrial ATP production. Shown is a heat map of median fold changes of probe set intensities between the treatment groups indicated in column titles (n = 10 mice/group). Each row represents one probe set. Only significantly different fold changes (P < 0.01) were shown in colors (red or green). NV stands for normal (db/+ or SDF) mice treated with vehicle. DV, DT1, DT3, and DT10 stand for diseased (db/db or HFD) mice treated with vehicle, 1, 3, and 10 mg/kg of RSG, respectively.

 
Among the regulated genes were those encoding key subunits of enzymes regulating the control points (22) in the TCA cycle, namely, pyruvate dehydrogenase, isocitrate dehydrogenase 3, and {alpha}-glutarate dehydrogenase, and those encoding electron transporters in OXPHOS, including cytochrome c and cytochrome c1. The rate of FAO is controlled by carnitinepalmitoyl transferase I (CPT-1) (22). CPT-1b, the major CPT-1 isoform in BAT (23), was significantly decreased in HFD mice (to 29% of that in SFD) and induced by RSG at a 10-mg/kg dose by 6.2- and 4.9-fold in db/db and HFD mice, respectively. In addition to enzymes/proteins directly involved in OXPHOS/TCA/FAO, those responsible for the transport of metabolites and intermediates for ATP production and FAO across mitochondrial membranes, including voltage-dependent anion channels, ATP/ADP shuttles, and carnitine/acyl carnitine shuttles, were suppressed in the adipose tissue from db/db and HFD mice and were dose-dependently induced by RSG (Fig. 1).

Transcription of UCPs was suppressed in db/db and HFD mice and induced by RSG.
To date, three UCP isoforms have been identified in mammalian cells (24): UCP-1, UCP-2, and UCP-3, which share >57% homology (25). In mice, UCP-1 is specifically expressed in mitochondria-rich BAT and plays a key role in nonshivering thermogenesis (25,26). Ectopic expression of UCP-1 in WAT mitigates obesity induced by genetic or dietary factors (25,26). UCP-3 is predominantly expressed in skeletal muscle, heart, and BAT and has been shown to facilitate FAO (27), whereas UCP-2 is localized to the pancreas, immune system, WAT, and the brain and has been linked to insulin secretion and modulation of inflammatory response (24,25).

UCP-1 was detected in the inguinal adipose tissue of db/+ mice and SFD mice, reaffirming the presence of BAT in the tissue (21). Interestingly, UCP-1 expression in the tissue from SFD mice was ~10-fold higher than that in db/+ mice (online appendix Table 1), indicating that the tissue from SFD mice had a greater proportion of the BAT-like component. UCP-1 expression in the tissue was lower in db/db than in db/+ mice and was even more dramatically decreased in HFD compared with SFD mice (Table 3). RSG treatment remarkably increased UCP-1 expression (by 37- and 34-fold, respectively) in both db/db and HFD mice.


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  		TABLE 3 Transcriptional regulation of UCPs, CIDEA, and transcription factors

 
Interestingly, the expression of cell death–inducing DFFA-like effector a (CIDEA), a modulator of UCP-1 and another marker of BAT-like tissue (5,28,29), was decreased in db/db and HFD mice compared with db/+ and SFD mice, respectively, and was increased by RSG in both models (Table 3). UCP-3 levels also decreased in db/db and HFD compared with db/+ and SFD mice, respectively, and were increased by RSG (Table 3). UCP-2 levels were not affected by diabetes/obesity or RSG treatment.

RSG-induced transcription of mitochondrial structural proteins.
To investigate whether the observed changes were associated with changed mitochondrial mass, the regulation of mitochondrial structural proteins not directly participating in metabolic activities was examined. These proteins include mitofilin, localized to mitochondrial inner membrane and regulating morphology of mitochondrial cristae (30); optic atrophy 1, anchored to mitochondrial inner membrane and localized to the intermembrane space and implicated in maintenance of mitochondrial genome and network (31); surfeit 1, localized to the inner membrane and involved in assembly of cytochrome c oxidase complex (32); and BCS1L, a human homologue of yeast BCS1 localized to the inner membrane and involved in the assembly of complex III of mitochondrial respiratory chain (33). Figure 2A shows that the transcription of these proteins was induced by RSG in db/db mice and so was that of mitofilin and optic atrophy 1 in HFD mice.


Figure 2
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  		FIG. 2. Transcriptional regulation of mitochondrial structural proteins (A) and mitochondrial ribosomal proteins, translocases of inner mitochondrial membranes (TIMMs) and translocases of outer mitochondrial membranes (TOMMs), and HSPs (B). Shown is a heat map of median fold changes of probe set intensities between the treatment groups indicated in column titles (n = 10 mice/group). Each row represents one probe set. Only significantly different fold changes (P < 0.01) were shown in colors (red or green). NV stands for normal (db/+ or SDF) mice treated with vehicle. DV, DT1, DT3, and DT10 stand for diseased (db/db or HFD) mice treated with vehicle, 1, 3, and 10 mg/kg of RSG, respectively.

 
RSG-induced transcription of proteins mediating mitochodrial gene translation, protein transport, and folding.
To further investigate the roles of diabetes/obesity and RSG on mitochondrial mass/biogenesis, transcription of genes directly participating in mitochondrial replication was examined. Figure 2B shows that 28 and 26% of transcripts representing mitochondrial ribosomal proteins were downregulated in db/db and HFD mice, respectively, whereas the rest of the mitochondrial ribosomal protein transcripts, with a few exceptions, were unchanged. Similarly, 27% transcripts encoding translocases that transport cytosolic proteins across mitochondria outer and inner membrane (translocases of outer mitochondrial membranes and translocases of inner mitochondrial membranes, respectively) were suppressed in both db/db and HFD mice. Furthermore, 42% transcripts for mitochondrial heat-shock proteins (HSPs)/chaperones, responsible for proper protein folding and transport, were downregulated, whereas the rest were unchanged, in db/db mice.

At 10 mg/kg, RSG treatment induced the transcription of 76 and 60% of mitochondrial ribosomal proteins and 80 and 70% of translocases of outer mitochondrial membranes and translocases of inner mitochondrial membranes, in db/db and HFD mice, respectively. The RSG effect was dose dependent, and the dose dependency was more evident in db/db than in HFD mice. In addition, RSG (10 mg/kg) induced in db/db and HFD mice 71 and 58% of the transcripts, respectively, for mitochondrial HSPs, including mitochondrial HSP70 (Hspa9a) and HSP60 (Hspd1), whereas there was no overall effect on cytosolic HSPs (such as Hspa4 and Tcp1, which belong to the cytosolic HSP70 and HSP60 family, respectively) or endoplasmic reticulum chaperones (e.g., calnexin, calreticulin, and GRP94), indicating that the induction by RSG was selective for mitochondrial proteins.

Regulation of transcription factors involved in mitochondrial biogenesis.
Mitochondrial biogenesis involves the integration of multiple transcriptional pathways controlling both nuclear and mitochondrial gene expression. PPAR{gamma} coactivators (PGC)-1{alpha} and -1ß have been implicated as key regulators of mitochondrial biogenesis in adipose tissue (3,6,34–37) and muscle (11,36–40). Table 3 shows that PGC-1ß transcription was suppressed in the inguinal fat in both db/db and HFD mice and was induced by RSG in both models. PGC-1{alpha} transcription in C57BL/6 mice was not influenced by diet (i.e., there was no difference between HFD and SDF mice); however, its transcription was suppressed in db/db compared with db/+ mice. RSG elicited expression of PGC-1{alpha} in HFD (P < 0.01) and db/db (P = 0.06) mice.

The expression of nuclear receptors ERR{alpha} and PPAR{alpha} was suppressed in db/db and HFD mice and induced by RSG. Receptor interacting protein (RIP) 140, a recently identified transcription corepressor negatively regulating mitochondrial biogenesis and metabolic functions in adipocytes (6,28), was induced in HFD but not in db/db mice. Surprisingly, RIP140 expression was induced by RSG in db/db mice and not affected in HFD mice. This indicates that RSG-induced mitochondrial biogenesis might not involve suppression of RIP140.

Transcription of cellular antioxidant enzymes were concordantly regulated with RSG-induced mitochondrial biogenesis.
Increased mitochondrial metabolic activity is associated with an increased chance of leaking O2–, leading to formation of other reactive oxygen species, followed by oxidative stress, cell injury, and eventually cell death. Figure 3 shows the transcription of antioxidant enzymes catalase, superoxide dismutase 1, superoxide dismutase 2, glutathione peroxidase 1, and methionine sulfoxide reductase A was generally increased by RSG. Meanwhile, RSG did not affect the transcription of mitochondrial proteins favoring apoptosis, such as Bax and Bad, or cytosolic regulators of apoptosis, such as caspases, in db/db and HFD mice.


Figure 3
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  		FIG. 3. Transcriptional regulation of antioxidant enzymes. Shown is a heat map of median fold changes of probe set intensities between the treatment groups indicated in column titles (n = 10 mice/group). Each row represents one probe set. Only significantly different fold changes (P < 0.01) were shown in colors (red or green). NV stands for normal (db/+ or SDF mice) treated with vehicle. DV, DT1, DT3, and DT10 stand for diseased (db/db or HFD mice) treated with vehicle, 1, 3, and 10 mg/kg of RSG, respectively.

 
Validation of microarray findings and mitochondrial biogenesis.
The transcription of 18 genes representing control point enzymes and structural proteins or those involved in mitochondrial replication or antioxidant enzymes were examined by QRT-PCR using inguinal adipose RNA samples from the db/db model. The results, generally consistent with the microarray data (online appendix Table 2A), supported the notion that mitochondrial transcription was downregulated in diabetes/obesity and induced by RSG. The microarray findings were also confirmed at the protein level by immunohistochemistry and histomorphometric analysis of a few representative mitochondrial markers (i.e., cytochrome C, HSP60, and UCP-1) (see below).

To test whether diabetes/obesity and RSG also affected mitochondrial gene expression in epididymal adipose tissue, predominantly WAT (21), the transcription of the 18 representative genes was examined by QRT-PCR. As expected, CIDEA was not detected, and UCP-1 expression was very low in epididymal adipose tissue. UCP-1 was surprisingly induced under the diabetes/obesity condition but was dramatically induced with RSG treatment. The regulation of the other genes was generally consistent with that in inguinal adipose tissue (online appendix Table 2B).

Staining of inguinal adipose tissue showed that adipocyte size in db/db mice was generally larger than that in db/+ mice (Fig. 4A) and decreased with RSG treatment (41). Cytochrome c, a mitochondrial marker, was significantly decreased in the db/db mice. RSG increased cytochrome c staining in virtually all adipocytes, indicating the conversion of mitochondria-poor to mitochondria-rich adipocytes. There was also increased presence of smaller, multilocular cells enriched with cytochrome c (Fig. 4A, arrows). The increase of total cytochrome c staining was RSG dose dependent (Fig. 4B), consistent with the microarray results. Similar observations were made with immunostaining of mitochondrial HSP60, another mitochondrial marker (Fig. 4C). UCP-1 staining was limited to the multilocular cells, confirming their brown adipocyte nature (Fig. 4D). RSG dose-dependently increased brown adipocyte numbers in inguinal adipose tissue (Fig. 4F).


Figure 4
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  		FIG. 4. Mitochondria and brown adipocyte content. Inguinal adipose tissues from db/+ or db/db mice with the indicated treatments (n = 10/group) were stained with mitochondrial markers. A, C, and D: Representative pictures from cytochrome c (A), mitochondrial HSP60 (C), or UCP-1 (D) staining. Arrows indicate cytochrome c–enriched brown adipocytes in A. Original magnification x200; when present, scale bar = 50 µm. B: Morphometric analysis of cytochrome c–stained areas. F: Averaged UCP-1–positive, brown adipocyte numbers in the acquired images (total area = 0.705 mm2). All numerical data were expressed as means ± SE. #P < 0.05 vs. db/db vehicle (Veh).

 
Mitochondrial DNA content in inguinal adipose tissue from db/db mice was slightly decreased compared with db/+ mice, but this did not reach statistical significance. However, mitochondrial DNA content in the tissue was increased by RSG dose dependently and, at 3- and 10-mg/kg doses, was significantly greater than vehicle-treated mice (Fig. 5A).


Figure 5
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  		FIG. 5. Mitochondrial DNA content (A) and citrate synthase activity (B). Relative mitochondrial DNA content and citrate synthase activity were determined in inguinal adipose tissues from db/+ or db/db mice with the indicated treatments (n = 10/group). Data were expressed as means ± SE. #P < 0.05 vs. db/db vehicle (Veh).

 
Citrate synthase, localized exclusively to the mitochondrial matrix, catalyzes the conversion of acetyl-CoA to citrate, the initial step in the TCA cycle. Citrate synthase activity has been used as a reference to determine changed mitochondrial function associated with mitochondrial biogenesis in adipose (3) and muscle (42). The activity in inguinal adipose tissue from db/db mice was significantly lower than that from db/+ mice (Fig. 5B). RSG dose-dependently increased the activity, reaching a plateau at 3 and 10 mg/kg.


   DISCUSSION
TOP
 ABSTRACT
 RESEARCH DESIGN AND METHODS
 RESULTS
 DISCUSSION
REFERENCES
 
The effects of diabetes/obesity and insulin sensitizers, such as RSG, on adipose mitochondrial biogenesis are only beginning to be understood and have not been systematically investigated in either db/db or HFD mice. The current study comprehensively evaluated mitochondrial nuclear DNA–encoded proteins involved in important metabolic functional pathways, including the control-point enzymes of each individual pathway. In addition, the regulation of transcription factors, mitochondrial structural proteins, and the machinery for mitochondrial replication were evaluated. In both mouse models, adipose mitochondrial gene transcription was overwhelmingly decreased in the disease states, and RSG dose-dependently increased the expression of many of the mitochondrial genes. The current results are consistent with recent observations in several in vivo models (3,8,9). The results on gene expression were extended by mitochondrial staining, quantification of mitochondrial DNA, and citrate synthase activity and further support a link between adipose mitochondria and the pathogenesis of diabetes/obesity.

The exact mechanisms by which adipose mitochondrial dysfunction and RSG-induced mitochondrial biogenesis contribute to whole-body energy homeostasis are unclear. Impaired mitochondria may lead to a lack of ATP (9), thereby attenuating triglyceride synthesis from fatty acids and carbohydrates in adipocytes, leading to a reduced adipose capacity for energy storage. Indeed, the insulin-sensitizing action of PPAR{gamma} agonists in muscle and liver is believed to be due to promoting triglyceride synthesis in adipose tissue and, thus, partitioning of circulating lipids away from muscle and the liver (1). A decrease in ATP may also impair the synthesis and secretion of adipokines that serve as endocrine signals. In fact, low serum levels of adiponectin, the most abundant secretory protein from adipocytes (43) and an adipokine that improves insulin sensitivity in other organs including the liver and muscle (44), is associated with diabetes/obesity in vivo. PPAR{gamma} activation increased circulating adiponectin levels in others’ (rev. in 1,44) and the current study (data not shown).

Adipose mitochondria also regulate whole-body energy metabolism via dissipating energy and generating heat in BAT. The inguinal adipose tissue consists of both BAT and WAT (21). The expression of BAT markers UCP-1, Cidea, and CPT-1b, were coordinately suppressed in the disease states and coordinately induced by RSG treatment in both models (Table 3). This indicates that the plasticity of the adipose tissue (diabetes/obesity induces the conversion of adipose from a semi-BAT phenotype to a more classical WAT phenotype) and RSG reverses the process by promoting the increase of mitochondria in pre-existing WAT (Fig. 4A; online appendix Table 2B) and the expansion of the BAT component (Fig. 4D and E). This supports the long-standing interest (e.g., 5,26) in converting WAT to BAT and transforming adipose tissue into fat-oxidizing machinery as a therapeutic approach for obesity and/or diabetes.

In the current study, RSG significantly increased mitochondrial activity. Inherent to increased mitochondrial activity is the potential of increased reactive oxygen species generation. Interestingly, RSG induced the transcription of antioxidant enzymes, responsible for removal of excess reactive oxygen species. This effect may prevent potential cell injury resulting from RSG-induced mitochondrial metabolic activity. The dual RSG actions on mitochondria and antioxidant enzymes could work through the upregulation of one or both of the PGC-1 proteins (Table 3) that have been shown to regulate both mitochondrial biogenesis and the antioxidant machinery (13,45). A recent study (46) also showed upregulation of antioxidant enzymes per se may be beneficial for improving insulin resistance.

In addition to genes involved in mitochondrial biology, a number of inflammation genes were coordinately regulated, but in an opposite direction to the mitochondrial genes, by diabetes/obesity and RSG treatment (data not shown), which is consistent with previous reports (47–49). Therefore, anti-inflammatory properties of PPAR{gamma} agonists represent yet another potential mechanism that may be involved in their efficacy in type 2 diabetes. The present study cannot discriminate whether mitochondrial effect is responsible for inflammation changes or vice versa. In addition, the study cannot rule out that RSG-induced improvements in mitochondrial function are an indirect consequence of improved glycemia; however, separate studies have indicated metformin, which decreased glucose levels in db/db mice, did not cause similar changes in adipose mitochondrial gene expression (online appendix Table 3). Furthermore, a similar effect on mitochondrial genes was observed with RSG in murine 3T3 L1, C3H10T1/2, and human primary adipocyte cultures that were free of inflammatory cell types and exposed to a constant concentration of glucose in the medium (J.X.R., Y.Q., unpublished data) (34,35). Taken together, this suggests that RSG is likely to have direct actions on adipose mitochondrial function.

In conclusion, in this study transcriptional profiling combined with phenotypic, molecular, and functional measurements indicates a deficiency in adipose mitochondrial function under diabetes/obesity conditions, and RSG treatment improves mitochondrial function. The results suggest a new area for the investigation of RSG action, that of promoting mitochondrial activity and health in metabolic tissues. These findings may bring new insights on the mechanisms of RSG action on diabetes/obesity treatment and new treatment approaches targeting adipose mitochondria.


   ACKNOWLEDGMENTS
 
The authors are thankful to Katherine Michelle Waters for providing excellent data from QRT-PCR, validating the microarray results; Matthew J. McVey for excellent assistance with the animal procedures; Drs. Randall Smith, Amit Bhattacharyya, and Dana Vanderwall for their excellent assistance in data analysis; Drs. Kirby Gottschalk and Richard Buckholz for kindly reviewing the manuscript and excellent comments; and Drs. Guanghui Hu, Qing Xie, Aixue Liu, Gregory Pahel, and Suzanne Neill for helpful discussions.


   FOOTNOTES
 
Published ahead of print at http://diabetes.diabetesjournals.org on 24 April 2007. DOI: 10.2337/db06-1135.

Additional information for this article can be found in an online appendix at http://dx.doi.org/10.2337/db06-1135.

The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

Received for publication August 14, 2006 and accepted in revised form April 11, 2007


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