Signaling role for phospholipase Cγ2 in platelet glycoprotein Ibα calcium flux and cytoskeletal reorganization -: Involvement of a pathway distinct from FcRγ chain and FcγRIIA

被引:94
作者
Mangin, P
Yuan, YP
Goncalves, I
Eckly, A
Freund, M
Cazenave, JP
Gachet, C
Jackson, SP
Lanza, F
机构
[1] Etablissement Francais Sang Alsace, INSERM, U311, F-67065 Strasbourg, France
[2] Monash Univ, Australian Ctr Blood Dis, Dept Med, Clayton, Vic 3127, Australia
关键词
D O I
10.1074/jbc.M302333200
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
Interaction of the platelet GPIb-V-IX complex with surface immobilized von Willebrand factor (vWf) is required for the capture of circulating platelets and their ensuing activation. In previous work, it was found that GPIb/vWf-mediated platelet adhesion triggers Ca2+ release from intracellular stores, leading to cytoskeletal reorganization and filopodia extension. Despite the potential functional importance of GPIb-induced cytoskeletal changes, the signaling mechanisms regulating this process have remained ill-defined. The studies presented here demonstrate an important role for phospholipase C ( PLC)-dependent phosphoinositide turnover for GPIb-dependent cytoskeletal remodeling. This is supported by the findings that the vWf-GPIb interaction induced a small increase in inositol 1,4,5-triphosphate (IP3) and that treating platelets with the IP3 receptor antagonist APB-2 or the PLC inhibitor U73122 blocked cytosolic Ca2+ flux and platelet shape change. Normal shape change was observed in Galpha(q)(-/-) mouse platelets, excluding a role for PLCbeta isoforms in this process. However, decreased shape change and Ca2+ mobilization were observed in mice lacking PLCgamma2, demonstrating that this isotype played an important, albeit incomplete, role in GPIb signaling. The signaling pathways utilized by GPIb involved one or more members of the Src kinase family as platelet shape change and Ca2+ flux were inhibited by the Src kinase inhibitors PP1 and PP2. Strikingly, shape change and Ca2+ release occurred independently of immunoreceptor tyrosine-based activation motif (ITAM)-containing receptors, because these platelet responses were normal in human platelets treated with the anti-FcgammaRIIA blocking monoclonal antibody IV.3 and in mouse platelets deficient in the FcRgamma chain. Taken together, these studies define an important role for PLCgamma2 in GPIb signaling linked to platelet shape change. Moreover, they demonstrate that GPIb-dependent calcium flux and cytoskeletal reorganization involves a signaling pathway distinct from that utilized by ITAM-containing receptors.
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收藏
页码:32880 / 32891
页数:12
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