Emerging role of Insig-1 in lipid metabolism and lipid disorders

Clin Chim Acta. 2020 Sep:508:206-212. doi: 10.1016/j.cca.2020.05.042. Epub 2020 May 24.

Abstract

Growing evidence has demonstrated that Insig-1 is intricately involved in lipid metabolism regulation and the progression of lipid disorders. Our review summarizes updated information on the role and underlying mechanisms of Insig-1 in lipid metabolism dyshomeostasis and lipid disorders. As a member of the insulin-induced gene family, insulin-induced gene 1 (Insig-1) is a six-span transmembrane protein embedded in the endoplasmic reticulum (ER) membrane. Insig-1 is widely involved in the maintenance of intracellular lipid metabolism homeostasis by controlling the activation of sterol regulatory element-binding proteins (SREBPs) and the degradation of 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGR). Growing experimental and clinical data have identified that Insig-1 reduces lipid accumulation in hepatocytes to relieve the development of nonalcoholic fatty liver disease (NAFLD), downregulates the plasma level of free cholesterol and protects β cells against lipotoxicity to alleviate diabetic dyslipidemia. In addition, Insig-1 suppresses adipogenesis and inhibits the differentiation of preadipocytes to prevent the occurrence of obesity. Insig-1 is a key regulatory factor that maintains intracellular lipid metabolism homeostasis and is a promising therapeutic target for lipid disorders.

Keywords: Diabetic dyslipidemia; Insig-1; Lipid metabolism; NAFLD; Obesity; SREBPs.

Publication types

  • Review

MeSH terms

  • Intracellular Signaling Peptides and Proteins*
  • Lipid Metabolism*
  • Lipids
  • Membrane Proteins / metabolism
  • Sterol Regulatory Element Binding Protein 1 / metabolism

Substances

  • Intracellular Signaling Peptides and Proteins
  • Lipids
  • Membrane Proteins
  • Sterol Regulatory Element Binding Protein 1