PR39 inhibits apoptosis in hypoxic endothelial cells - Role of inhibitor apoptosis protein-2

Article

关键词: RAT CARDIAC MYOCYTES;    ANTIBACTERIAL PEPTIDE;    MESSENGER-RNA;    BCL-2;    EXPRESSION;    ELEMENT;    BINDING;    PR-39;    DEGRADATION;    ACTIVATION;   

DOI  :  10.1161/01.CIR.0000124067.35915.E0

来源: SCIE

【 摘 要 】

Background - PR39 is a proline- and arginine-rich peptide implicated in wound healing and myocardial ischemia protection. To determine the potential mechanisms of PR39 in ischemia, we examined the role of PR39 in hypoxia-induced apoptosis in vascular endothelial cells. Methods and Results - Hypoxia results in an increase of apoptosis in bovine aortic endothelial cells (BAECs), as determined by terminal deoxynucleotidyl transferase - mediated dUTP biotin nick-end labeling (TUNEL) analysis and caspase-3 activity. Hypoxia induced 66.2 +/- 2.7% TUNEL-positive cells, whereas in the presence of synthesized PR39 peptide, TUNEL-positive cells were reduced to 29.6 +/- 1.9% (P < 0.05). After 24 hours of hypoxia, the addition of PR39 reduced caspase-3 activity to 3.17 +/- 0.47 pMol/min from 10.52 +/- 0.55 pMol/min in hypoxic BAECs. Moreover, PR39 increased inhibitor of apoptosis protein-2 (IAP-2) gene and protein expression by 3-fold in a time- and dose-dependent manner. The induction of IAP-2 by PR39 conferred an increase in IAP-2 gene transcription and IAP-2 mRNA stability. Furthermore, inhibiting IAP-2 with second mitochondria-derived activator of caspase (Smac) and with small interfering RNA targeting IAP-2 abrogated the ability of PR39 to reduce caspase-3 activity. Conclusions - We provide the first direct evidence for PR39 as an antiapoptotic factor in endothelial cells during hypoxia. These data suggest that PR39 inhibits hypoxia-induced apoptosis and decreases caspase-3 activity in endothelial cells through an increase of IAP-2 expression.

【 授权许可】

Free