The lysophosphatidic acid 2 receptor mediates down-regulation of Siva-1 to promote cell survival

被引:55
作者
Lin, Fang-Tsyr [1 ]
Lai, Yun-Ju [1 ]
Makarova, Natalia [3 ]
Tigyi, Gabor [3 ]
Lin, Weei-Chin [1 ,2 ]
机构
[1] Univ Alabama, Dept Cell Biol, Birmingham, AL 35294 USA
[2] Univ Alabama, Dept Med, Div Hematol & Oncol, Birmingham, AL 35294 USA
[3] Univ Tennessee, Ctr Hlth Sci, Dept Physiol, Memphis, TN 38163 USA
关键词
D O I
10.1074/jbc.M705025200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lysophosphatidic acid (LPA) promotes cell survival through the activation of G protein-coupled LPA receptors. However, whether different LPA receptors activate distinct anti-apoptotic signaling pathways is not yet clear. Here we report a novel mechanism by which the LPA(2) receptor targets the proapoptotic Siva-1 protein for LPA-dependent degradation, thereby attenuating Siva-1 function in DNA damage response. The carboxylterminal tail of the LPA2 receptor, but not LPA(1) or LPA(3) receptor, specifically associates with the carboxyl cysteine-rich domain of Siva-1. Prolonged LPA stimulation promotes the association of Siva-1 with the LPA(2) receptor and targets both proteins for ubiquitination and degradation. As a result, adriamycin-induced Siva-1 protein stabilization is attenuated by LPA in an LPA(2)-dependent manner, and the function of Siva-1 in promoting DNA damage-induced apoptosis is inhibited by LPA pretreatment. Consistent with this result, inhibition of the LPA2 receptor expression increases Siva-1 protein levels and augments adriamycin-induced caspase-3 cleavage and apoptosis. Together, these findings reveal a critical and specific role for the LPA(2) receptor through which LPA directly inactivates a critical component of the death machinery to promote cell survival.
引用
收藏
页码:37759 / 37769
页数:11
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