Adipocyte-Specific Expression of PGC1α Promotes Adipocyte Browning and Alleviates Obesity-Induced Metabolic Dysfunction in an HO-1-Dependent Fashion

Figures

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  Figure 1. Effects of the adipocyte-specific overexpression of PGC-1α in high-fat-diet (HFD.)-fed mice. (A) Tissue expression levels of adipo-PGC1α; (B) glucose tolerance test; and (C) area under curve; (data are expressed as mean ± SEM (n = 5); * p < 0.05 versus lean; # p < 0.05 vs.HFD.

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  Figure 2. Effects of adipocyte-specific overexpression of PGC-1α in high-fat-diet (HFD)-fed mice compared to lean and untreated HFD mice. Histological analysis of adipose tissue using Hematoxylin–Eosin of (A) lean, (B) HFD, and (C) HFD+ PGC-1α mice; (D) Adipocyte number and (E) adipocyte diameter. Masson trichrome staining photomicrographs of PGC-1α expression at the adipose tissue level of (F) lean, (G) HFD, and (H) HFD + PGC-1α mice; (I) Percentage of adipocyte fibrosis, (J–M) liver macrosteatosis, and (N) liver lipid droplet diameter. Bar 20 μm. Data are expressed as mean ± S.E.M. (n = 5); * p < 0.05 versus lean; # p < 0.05 vs. HFD.

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  Figure 3. Effects of the adipocyte-specific overexpression of PGC-1α in high-fat-diet (H.F.D.)-fed mice compared to lean and untreated HFD mice. Iimmunofluorescence photomicrographs of PGC-1α expression (red staining) at the adipose tissue level of (A) lean, (B) H.F.D., and (C) HFD + PGC-1α mice. Graph (D) summarizes the immune morphometrical measurement of the nuclear localization of PGC-1α (A.U.). Quantitative gene expression analysis of (E) PGC-1α, HO-1, Mfn1, and Mfn2; (F) Fis1 and NOV/CCN3 in adipose tissue of Transgenic-adipo-PGC-1α mice fed with a high-fat diet. Data are expressed as mean ± S.E.M. (n = 5); **** p < 0.05 versus lean; *** p < 0.05 versus HFD,* p < 0.05 versus HFD. ** p < 0.05 versus lean (G) Oxygen consumption rates (OCR) in PGC-1α knockdown (shPGC1α), overexpression (ORF PGC-1α), and control cultured adipocytes, n = 3. **** p < 0.005, versus control. The maximal respiration capacity represents the sum of all physiological mitochondrial oxygen consumption.

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  Figure 4. Effects of the Transgenic-adipo-PGC-1α treatment on the key proteins involved in mitochondrial fission and biogenesis and adipocyte browning. Representative Western blot analysis of (A) PGC-1α and HO-1 (B,C), (D–G) MFN2, Fis1, and UCP1, (H–K) Sirt1, Adiponectin and MnSOD2 with their corresponding β-actin in the adipose tissue of lean, HFD and Transgenic-adipo-PGC-1α mice. Data are expressed as mean ± S.E.M. (n = 5); * p < 0.05 versus lean; # p < 0.05 versus HFD.

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  Figure 5. Expression of inflammatory mediators and insulin signaling in the adipose tissue of lean, high-fat-diet (H.F.D.)-fed, and Transgenic-adipo-PGC-1α mice. Representative Western blot analysis of (A–D) MEST, NOV/CCN3 and TWIST, (E–G) FGF21 and phosphorylated insulin receptor tyrosine 972 (pIRTyr972), (H–J) pAKT and pAMPK with their corresponding A.K.T. and AMPK in the adipose tissue of lean, H.F.D., and Transgenic-adipo-PGC-1α mice. Data are expressed as mean ± S.E.M. (n = 5); * p < 0.05 vs. lean; # p < 0.05 vs. H.F.D.

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  Figure 6. The mRNA expression of (A) Jun proto-oncogene (Jun), (B) lamin A (Lmna), (C) nuclear receptor subfamily 1 group H member 3 (Nr1h3), (D) R.B. transcriptional corepressor 1 (Rb1), (E) retinoid X receptor alpha (Rxra), and (F) secreted frizzled-related protein 1 (Sfrbf1) in the adipose tissue of lean, high-fat-diet (H.F.D.)-fed and Transgenic-adipo-PGC-1α mice. Data are expressed as mean ± S.E.M. (n = 5); * p < 0.05, ** p < 0.005 vs. lean; # p < 0.05, ## p < 0.005 vs. HFD.

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  Figure 7. The mRNA expression of (A) adiponectin, (B) insulin receptor precursor (Insr), (C) lipoprotein lipase (Lpl), (D) Prdm16, (E) Sonic hedgehog (Shh), (F) silent mating-type information regulation 2 homolog (Situin1), (G) solute carrier family 2 member 4 (Slc2), (H) Tafazzin (Taz), (I) Uncoupling protein 1 (UCP1), and (J) vitamin D receptor (Vdr) in the adipose tissue of lean, high-fat-diet (H.F.D.)-fed and Transgenic-adipo-PGC-1α mice. Data are expressed as mean ± S.E.M. (n = 5); * p < 0.05, ** p < 0.005 vs. lean; # p < 0.05, ## p < 0.005 vs. HFD.

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  Figure 8. Effects of SnPP treatment on insulin-receptor phosphorylation and mitochondrial fission in the adipose tissue of Transgenic-adipo-PGC-1α mice fed with high-fat diet (H.F.D.). Representative Western blots of (A) phosphorylated insulin-receptor substrate 1 serine307 (pIRS1 ser307) and phosphorylated insulin-receptor tyrosine972 (pIR Tyr972) with the corresponding quantitation to β-actin (B,C). (D) Representative Western blots of FGF21, CREG1, and OPA1 with the corresponding quantitation to β-actin (E–G). Data are expressed as mean ± S.E.M. (n = 5); * p < 0.05 versus lean; # p < 0.05 versus H.F.D.; + p < 0.05 vs. PGC-1α.

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  Figure 9. Effects of SnPP treatment on browning markers and AMPK phosphorylation in the adipose tissue of Transgenic-adipo-PGC-1α mice fed with a high-fat diet. Representative Western blots of (A) PGC-1α, HO-1, pAMPK, and AMPK with the corresponding quantitation to β-actin (B–D). (E–G) UCP1 and PRDM16. Data are expressed as mean ± S.E.M. (n = 5); * p < 0.05 vs. lean; # p < 0.05 versus H.F.D.; + p < 0.05 vs. PGC-1α. Effects of SnPP treatment on inflammatory mediators and transforming growth factor β (TGF-β) signaling (pSmad 1–5 and pSmad 2) in the adipose tissue of Transgenic-adipo-PGC-1α mice fed with a high-fat diet. Representative Western blots of (H–J) NOV/CCN3 (H) and IL-6 (J) with the corresponding quantitation to β-actin; Representative Western blots of pSmad 1–5 and pSmad2 with the corresponding quantitation to β-actin (9; K–M); and phosphorylation of pP38 MAPK (9N) with the corresponding quantitation to pP38 MAPK. Data are expressed as mean ± S.E.M. (n = 5); * p < 0.05 versus lean; # p < 0.05 versus H.F.D.; + p < 0.05 versus PGC-1α.

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  Figure 10. Schematic depiction of the postulated hypothesis showing that adipocyte-specific PGC-1α expression coordinates HO-1 to induce the conversion of white adipocytes to the beige phenotype, and improves mitochondrial biogenesis/fusion, energy expenditure, and insulin sensitivity as well as vascular function. Adipo-PGC-1α inhibits TGF-β/Smad signaling (pSmad 1–5, Smad 2 and P38MAPK) and inflammatory adipokines (NOV/CCN3 and IL-6). Selective expression of adipocyte PGC-1α provides a genetic approach for obesity, fatty liver, and associated metabolic syndrome management.