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Nat Cell Biol. 2001 Nov;3(11):1020-4.

A new phospholipase-C-calcium signalling pathway mediated by cyclic AMP and a Rap GTPase.

Author information

1
Institut f├╝r Pharmakologie, Universit├Ątsklinikum Essen, 45122 Essen, Germany. martina.schmidt@uni-essen.de

Abstract

Stimulation of phosphoinositide-hydrolysing phospholipase C (PLC) generating inositol-1,4,5-trisphosphate is a major calcium signalling pathway used by a wide variety of membrane receptors, activating distinct PLC-beta or PLC-gamma isoforms. Here we report a new PLC and calcium signalling pathway that is triggered by cyclic AMP (cAMP) and mediated by a small GTPase of the Rap family. Activation of the adenylyl cyclase-coupled beta2-adrenoceptor expressed in HEK-293 cells or the endogenous receptor for prostaglandin E1 in N1E-115 neuroblastoma cells induced calcium mobilization and PLC stimulation, seemingly caused by cAMP formation, but was independent of protein kinase A (PKA). We provide evidence that these receptor responses are mediated by a Rap GTPase, specifically Rap2B, activated by a guanine-nucleotide-exchange factor (Epac) regulated by cAMP, and involve the recently identified PLC-epsilon isoform.

PMID:
11715024
DOI:
10.1038/ncb1101-1020
[Indexed for MEDLINE]

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