Mannon P J, Raymond J R
Duke University Medical Center, Durham, North Carolina, USA.
Biochem Biophys Res Commun. 1998 May 8;246(1):91-4. doi: 10.1006/bbrc.1998.8577.
The neuropeptide Y/peptide YY (PYY) Y1 receptor subtype mediates proliferative responses. This report identifies effector molecules which mediate mitogen-activated protein kinase (MAPK) phosphorylation by Y1 receptor activation in transfected CHO cells. Pertussis toxin pretreatment abolishes this effect, indicating involvement of Gi or G(o) proteins. Inhibition of protein kinase C (PKC) also blocks PYY-induced MAPK phosphorylation. Additionally in this cell model PYY causes an increase in GTP binding to Ras protein, and cotransfection of dominant negative constructs for Ras and Raf blocks PYY effects on MAPK. These data suggest a novel mechanism for Y1 receptor coupling to MAPK, which is at once pertussis toxin-sensitive as well as PKC- and Ras-dependent.
神经肽Y/肽YY(PYY)的Y1受体亚型介导增殖反应。本报告鉴定了在转染的CHO细胞中通过Y1受体激活介导丝裂原活化蛋白激酶(MAPK)磷酸化的效应分子。百日咳毒素预处理可消除此效应,表明Gi或G(o)蛋白参与其中。蛋白激酶C(PKC)的抑制也可阻断PYY诱导的MAPK磷酸化。此外,在此细胞模型中,PYY导致GTP与Ras蛋白结合增加,并且共转染Ras和Raf的显性负性构建体可阻断PYY对MAPK的作用。这些数据提示了Y1受体与MAPK偶联的一种新机制,该机制对百日咳毒素敏感,同时依赖PKC和Ras。