Diabetes Obesity and Metabolism Institute, Icahn School of Medicine at Mount Sinai, 1 Gustave Levy Place, Box 1152, New York, NY 10029, USA.
Biochim Biophys Acta Mol Basis Dis. 2018 Apr;1864(4 Pt A):1160-1171. doi: 10.1016/j.bbadis.2018.01.025.
Accumulation of dysfunctional white adipose tissues increases risks for cardiometabolic diseases in obesity. In addition to white, brown or brite adipose tissues are also present in adult humans and increasing their amount may be protective. Therefore, understanding factors regulating the amount and function of each adipose depot is crucial for developing therapeutic targets for obesity and its associated metabolic diseases. The transforming growth factor beta (TGFβ) superfamily, which consists of TGFβ, BMPs, GDFs, and activins, controls multiple aspects of adipose biology. This review focuses on the recent development in understanding the role of TGFβ superfamily in the regulation of white, brite and brown adipocyte differentiation, adipose tissue fibrosis, and adipocyte metabolic and endocrine functions. TGFβ family and their antagonists are produced locally within adipose tissues and their expression levels are altered in obesity. We also discuss their potential contribution to adipose tissue dysfunction in obesity.
功能失调的白色脂肪组织积累会增加肥胖患者患心血管代谢疾病的风险。除了白色脂肪组织,成年人体内还存在棕色或米色脂肪组织,增加其数量可能具有保护作用。因此,了解调节每个脂肪库数量和功能的因素对于开发肥胖及其相关代谢疾病的治疗靶点至关重要。转化生长因子β(TGFβ)超家族由 TGFβ、BMPs、GDFs 和激活素组成,它控制着脂肪生物学的多个方面。这篇综述重点介绍了近年来对 TGFβ 超家族在调节白色、米色和棕色脂肪细胞分化、脂肪组织纤维化以及脂肪细胞代谢和内分泌功能方面的作用的理解的最新进展。TGFβ 家族及其拮抗剂在脂肪组织内局部产生,其表达水平在肥胖中发生改变。我们还讨论了它们对肥胖症中脂肪组织功能障碍的潜在贡献。