Mechanism of Ferroptosis and Its Role in Type 2 Diabetes Mellitus

J Diabetes Res. 2021 Jun 28:2021:9999612. doi: 10.1155/2021/9999612. eCollection 2021.

Abstract

Ferroptosis is a novel form of nonapoptotic regulated cell death (RCD). It features iron-dependent lipid peroxide accumulation accompanied by inadequate redox enzymes, especially glutathione peroxidase 4 (GPX4). RAS-selective lethal 3 (RSL3), erastin, and ferroptosis inducing 56 (FIN56) induce ferroptosis via different manners targeting GPX4 function. Acyl-CoA synthetase long-chain family 4 (ACSL4), lysophosphatidylcholine acyltransferase 3 (LPCAT3), and lipoxygenases (LOXs) participate in the production of lipid peroxides. Heat shock protein family B member 1 (HSPB1) and nuclear receptor coactivator 4 (NCOA4) regulate iron homeostasis preventing ferroptosis caused by the high concentration of intracellular iron. Ferroptosis is ubiquitous in our body as it exists in both physiologic and pathogenic processes. It is involved in glucose-stimulated insulin secretion (GSIS) impairment and arsenic-induced pancreatic damage in the pathogenesis of diabetes. Moreover, iron and the iron-sulfur (Fe-S) cluster influence each other, causing mitochondrial iron accumulation, more reactive oxygen species (ROS) production, endoplasmic reticulum (ER) stress, failure in biosynthesis of insulin, and ferroptosis in β-cells. In addition, ferroptosis also engages in the pathogenesis of diabetic complications such as myocardial ischemia and diabetic cardiomyopathy (DCM). In this review, we summarize the mechanism of ferroptosis and especially its association with type 2 diabetes mellitus (T2DM).

Publication types

  • Review

MeSH terms

  • Apoptosis Regulatory Proteins / metabolism
  • Diabetes Complications / etiology
  • Diabetes Complications / physiopathology
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / physiopathology*
  • Diabetic Cardiomyopathies / etiology
  • Diabetic Cardiomyopathies / physiopathology*
  • Ferroptosis / physiology*
  • Humans
  • Iron / metabolism*
  • Lipid Peroxidation*
  • Metabolic Networks and Pathways
  • Mevalonic Acid / metabolism
  • Mitochondrial Proteins / metabolism
  • Myocardial Ischemia / etiology
  • Myocardial Ischemia / physiopathology*
  • Phospholipid Hydroperoxide Glutathione Peroxidase / metabolism
  • Reactive Oxygen Species / metabolism

Substances

  • ferroptosis suppressor protein 1, human
  • Apoptosis Regulatory Proteins
  • Mitochondrial Proteins
  • Reactive Oxygen Species
  • Iron
  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • Mevalonic Acid