Novel pathogenesis: regulation of apoptosis by Apelin/APJ system

Acta Biochim Biophys Sin (Shanghai). 2017 Jun 1;49(6):471-478. doi: 10.1093/abbs/gmx035.

Abstract

Apelin is the endogenous peptide APJ receptor, while APJ is a member of the G protein-coupled receptors family. Recent evidence strongly suggests that Apelin/APJ system influences apoptosis in various diseases through different signal pathways. In this review, we discuss the possible mechanisms by which the Apelin/APJ system inhibits apoptosis, including the phosphatidylinositol-3-kinase (PI3K)/Akt, ERK1/2, caspase signaling, and autophagy pathway. We also summarize the role of Apelin/APJ system in apoptosis in myocardial ischemia-reperfusion (I/R) injury, pulmonary artery hypertension, retinal neovascular disease, acute renal injury, skeletal homeostasis, and gastrointestinal diseases. Apelin/APJ system decreases myocardial infarction size and alleviates myocardial I/R injury by inhibiting cardiomyocytes apoptosis. However, Apelin/APJ system improves pulmonary artery hypertension via increasing apoptosis. Apelin/APJ system exerts neuroprotective effect by blocking apoptosis and participates in the recovery of retinal neovascular disease by suppressing apoptosis. Apelin/APJ system also shows anti-apoptotic effect against acute renal injury and plays a role in regulating skeletal homeostasis. In gastrointestinal disease, Apelin/APJ system plays a potential physiological role in gastrointestinal cytoprotection by regulating apoptosis. We hope that a better understanding of the Apelin/APJ system will help to discover new disease pathogenesis and find possible therapeutic targets of the Apelin/APJ system essential for various diseases.

Keywords: Apelin/APJ system; apoptosis; pathogenesis; therapeutic target.

Publication types

  • Review

MeSH terms

  • Acute Kidney Injury / metabolism
  • Animals
  • Apelin / metabolism*
  • Apelin Receptors / metabolism*
  • Apoptosis*
  • Autophagy
  • Humans
  • Models, Biological
  • Myocardial Reperfusion Injury / metabolism
  • Signal Transduction*

Substances

  • APLN protein, human
  • APLNR protein, human
  • Apelin
  • Apelin Receptors