Diacylglycerol kinase δ regulates protein kinase C and epidermal growth factor receptor signaling

被引:76
作者
Crotty, Tracy
Cai, Jinjin
Sakane, Fumio
Taketomi, Akinobu
Prescott, Stephen M.
Topham, Matthew K.
机构
[1] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Internal Med, Salt Lake City, UT 84112 USA
关键词
JUN NH2-TERMINAL KINASE; EGF RECEPTOR; MICE LACKING; PHOSPHORYLATION; ZETA; CLONING; ACTIVATION; EXPRESSION; MECHANISM; ENDOSOME;
D O I
10.1073/pnas.0604104103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Diacylglycerol kinases (DGKs) phosphorylate diacylglycerol (DAG) to terminate its signaling. To study DGK delta, we disrupted its gene in mice and found that DGK delta deficiency reduced EGF receptor (EGFR) protein expression and activity. Similar to EGFR knockout mice, DGK delta-deficient pups were born with open eyelids and died shortly after birth. PKCs are activated by DAG and phosphorylate EGFR to reduce its expression and activity. We found DAG accumulation, increased threonine phosphorylation of EGFR, enhanced phosphorylation of other PKC substrates, and increased PKC autophosphorylation in DGK delta knockout cells, indicating that DGK delta regulates EGFR by modulating PKC signaling.
引用
收藏
页码:15485 / 15490
页数:6
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