Roles of G proteins and their GTPase-activating proteins in platelets

被引:1
|
作者
O'Donoghue, Lorna [1 ,2 ]
Smolenski, Albert [1 ,2 ]
机构
[1] Univ Coll Dublin, UCD Conway Inst, UCD Sch Med, Dublin, Ireland
[2] Royal Coll Surgeons Ireland, Irish Ctr Vasc Biol, 123 St Stephens Green, Dublin 2, Ireland
关键词
DENSE GRANULE SECRETION; THROMBUS FORMATION; HEMOSTATIC RESPONSE; ESSENTIAL MEDIATOR; FAMILY-MEMBERS; MICE LACKING; RHO GTPASES; RAP1; DEFICIENCY; DOMAIN;
D O I
10.1042/BSR20231420
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
Platelets are small anucleate blood cells supporting vascular function. They circulate in a quiescent state monitoring the vasculature for injuries. Platelets adhere to injury sites and can be rapidly activated to secrete granules and to form platelet/platelet aggregates. These responses are controlled by signalling networks that include G proteins and their regulatory guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs). Recent proteomics studies have revealed the complete spectrum of G proteins, GEFs, and GAPs present in platelets. Some of these proteins are specific for platelets and very few have been characterised in detail. GEFs and GAPs play a major role in setting local levels of active GTP-bound G proteins in response to activating and inhibitory signals encountered by platelets. Thus, GEFs and GAPs are highly regulated themselves and appear to integrate G protein regulation with other cellular processes. This review focuses on GAPs of small G proteins of the Arf, Rab, Ras, and Rho families, as well as of heterotrimeric G proteins found in platelets.
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页数:29
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