Apoptosis

, Volume 12, Issue 1, pp 247–254

Apelin suppresses apoptosis of human osteoblasts

  • Hui Xie
  • Ling-Qing Yuan
  • Xiang-Hang Luo
  • Jiao Huang
  • Rong-Rong Cui
  • Li-Juan Guo
  • Hou-De Zhou
  • Xian-Ping Wu
  • Er-Yuan Liao
Article

DOI: 10.1007/s10495-006-0489-7

Cite this article as:
Xie, H., Yuan, LQ., Luo, XH. et al. Apoptosis (2007) 12: 247. doi:10.1007/s10495-006-0489-7

Abstract

Objectives: Apelin is a recently discovered peptide that is the endogenous ligand for the orphan G-protein-coupled receptor APJ. Adipocytes can express and secrete apelin. Osteoblast can express apelin and APJ. The aim of this study was to investigate the action of apelin on apoptosis of human osteoblasts. Results: Apelin inhibited human osteoblasts apoptosis induced by serum deprivation. Suppression of APJ with small-interfering RNA (siRNA) abolished the anti-apoptotic activity of apelin. Our study also showed an increased Bcl-2 protein expression and decreased Bax protein expression under the treatment of apelin. Apelin decreased cytochrome c release and caspase-3 activation in human osteoblasts. Apelin activated phosphatidylinositol-3 kinase (PI-3 kinase) and Akt. The apelin-induced activation of Akt was blocked by suppression of APJ with siRNA. LY294002 (a PI-3 kinase inhibitor) or 1L-6-hydroxymethyl-chiro-inositol 2-(R)-2-O-methyl-3-O-octadecylcarbonate (HIMO; an Akt inhibitor) abolished apelin induced activation of Akt, and, LY294002 or HIMO abolished the anti-apoptotic activity of apelin. Furthermore, apelin protects against apoptosis induced by the glucocorticoid dexamethasone. Conclusions: Apelin suppresses serum deprivation-induced apoptosis of human osteoblasts and the anti-apoptotic action is mediated via the APJ/PI-3 kinase/Akt signaling pathway.

Keywords

ApelinAPJOsteoblastApoptosisPhosphatidylinositol-3 kinaseAkt

Copyright information

© Springer Science + Business Media, LLC 2006

Authors and Affiliations

  • Hui Xie
    • 1
  • Ling-Qing Yuan
    • 1
  • Xiang-Hang Luo
    • 1
  • Jiao Huang
    • 1
  • Rong-Rong Cui
    • 1
  • Li-Juan Guo
    • 1
  • Hou-De Zhou
    • 1
  • Xian-Ping Wu
    • 1
  • Er-Yuan Liao
    • 1
  1. 1.Institute of Endocrinology & MetabolismThe Second Xiangya Hospital of Central South UniversityChangshaPR China