PPARs-Orchestrated Metabolic Homeostasis in the Adipose Tissue

• Published in: International journal of molecular sciences Vol. 22; no. 16; p. 8974
• Main Authors: Sun, Chen, Mao, Shuyu, Chen, Siyu, Zhang, Wenxiang, Liu, Chang
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 20.08.2021; MDPI
• Subjects: Adipocytes; Binding sites; Body fat; Cloning; Cytokines; Energy; Fatty acids; Gene expression; Glucose; Homeostasis; Insulin resistance; Ligands; Lipids; Metabolic syndrome; Musculoskeletal system; Proteins; Respiration; Review; Weight control
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms22168974

It has been more than three decades since peroxisome proliferator-activated receptors (PPARs) were first discovered. Many investigations have revealed the central regulators of PPARs in lipid and glucose homeostasis in response to different nutrient conditions. PPARs have attracted much attention due to their ability to improve metabolic syndromes, and they have also been proposed as classical drug targets for the treatment of hyperlipidemia and type 2 diabetes (T2D) mellitus. In parallel, adipose tissue is known to play a unique role in the pathogenesis of insulin resistance and metabolic syndromes due to its ability to “safely” store lipids and secrete cytokines that regulate whole-body metabolism. Adipose tissue relies on a complex and subtle network of transcription factors to maintain its normal physiological function, by coordinating various molecular events, among which PPARs play distinctive and indispensable roles in adipocyte differentiation, lipid metabolism, adipokine secretion, and insulin sensitivity. In this review, we discuss the characteristics of PPARs with special emphasis on the roles of the different isotypes in adipocyte biology.