Role of peroxisome proliferator-activated receptor gamma Pro12Ala polymorphism in human adipose tissue: assessment of adipogenesis and adipocyte glucose and lipid turnover

• Published in: Adipocyte Vol. 7; no. 4; pp. 285 - 296
• Main Authors: Kamble, Prasad G., Pereira, Maria J., Gustafsson, Stefan, Lundkvist, Per, Castillejo-López, Casimiro, Fall, Tove, Ingelsson, Erik, Eriksson, Jan W.
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 01.01.2018
• Subjects: human adipose tissue; metabolism and adipogenesis; PPARG Pro12Ala; PPARγ Pro12Ala; Research Paper; human adipose tissue; metabolism and adipogenesis; PPARγ Pro12Ala
• ISSN: 2162-3945; 2162-397X; 2162-397X
• DOI: 10.1080/21623945.2018.1503030

The protective mechanisms of peroxisome proliferator-activated receptor gamma (PPARγ) Pro12Ala polymorphism in type 2 diabetes (T2D) are unclear. We obtained subcutaneous adipose tissue (AT) before and 3 h after oral glucose (OGTT) in carriers and non-carriers of the Ala allele (12 Pro/Pro, 15 Pro/Ala, and 13 Ala/Ala). Adipogenesis, adipocyte glucose uptake and lipolysis as well as PPARγ target gene expression were investigated and compared between the genotype groups. During fasting and post-OGTT, neither basal nor insulin-stimulated adipocyte glucose uptake differed between genotypes. Compared to fasting, a decreased hormone-sensitive lipase gene expression in Pro/Pro (p < 0.05) was accompanied with a higher antilipolytic effect of insulin post-OGTT (p < 0.01). The adipocyte size was similar across groups. Preadipocyte differentiation rates between Pro/Pro and Ala/Ala were unchanged. In conclusion, no major differences in AT differentiation, glucose uptake, lipolysis or expression of PPARγ target genes were observed between different PPARγ Pro12Ala genotypes. Albeit small, our study may suggest that other pathways in AT or effects exerted in other tissues might contribute to the Pro12Ala-mediated protection against T2D.