A Nonapoptotic Role for BAX and BAK in Eicosanoid Metabolism

被引:4
|
作者
Zhang, Tejia [1 ]
Walensky, Loren D. [2 ,3 ,4 ]
Saghatelian, Alan [1 ]
机构
[1] Salk Inst Biol Studies, Clayton Fdn Labs Peptide Biol, La Jolla, CA 92037 USA
[2] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02215 USA
[3] Harvard Univ, Boston Childrens Hosp, Sch Med, Boston, MA 02215 USA
[4] Harvard Univ, Dana Farber Canc Inst, Sch Med, Linde Program Canc Chem Biol, Boston, MA 02215 USA
关键词
PROSTACYCLIN; APOPTOSIS; BCL-2; MITOCHONDRIA; INFLAMMATION; FIBROBLASTS; RECEPTORS; PROTEINS; KINETICS; BIOLOGY;
D O I
10.1021/acschembio.5b00168
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
BCL-2 proteins are key regulators of programmed cell death. The interplay between pro and antiapoptotic BCL-2 members has important roles in many cancers. In addition to their apoptotic function, recent evidence supports key, nonapoptotic roles for several BCL-2 proteins: We used an unbiased lipidomics strategy to reveal that the proapoptotic proteins BAX, and to a lesser extent BAK, regulate the cellular inflammatory response by mediating COX-2 expression and prostaglandin biosynthesis: COX-2 upregulation in response to the bacterial endotoxin lipopolysaccharide is blunted in the absence of BAX, and Bax(-/-) Mouse embryonic fibroblasts display altered kinetics of NF kappa B and MAPK. signaling following: endotoxin treatment.; Our approach uncovers a novel, nonapoptotic function for BAX in regulation of the cellular inflammatory response and suggests that inflammation and apoptosis are more tightly connected than previously anticipated.
引用
收藏
页码:1398 / 1403
页数:6
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