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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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