Jarvis Gavin E, Best Denise, Watson Steve P
Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX1 3QT, UK.
Biochem J. 2004 Nov 1;383(Pt. 3):581-8. doi: 10.1042/BJ20040654.
We have investigated the ability of collagen to induce signalling and functional responses in suspensions of murine platelets deficient in the FcRgamma (Fc receptor gamma) chain, which lack the collagen receptor GPVI (glycoprotein VI). In the absence of the FcRgamma chain, collagen induced a unique pattern of tyrosine phosphorylation which was potentiated by the thromboxane analogue U46619. Immunoprecipitation studies indicated that neither collagen alone nor the combination of collagen plus U46619 induced phosphorylation of the GPVI-regulated proteins Syk and SLP-76 (Src homology 2-containing leucocyte protein of 76 kDa). A low level of tyrosine phosphorylation of phospholipase Cgamma2 was observed, which was increased in the presence of U46619, although the degree of phosphorylation remained well below that observed in wild-type platelets (approximately 10%). By contrast, collagen-induced phosphorylation of the adapter ADAP (adhesion- and degranulation-promoting adapter protein) was substantially potentiated by U46619 to levels equivalent to those observed in wild-type platelets. Collagen plus U46619 also induced significant phosphorylation of FAK (focal adhesion kinase). The functional significance of collagen-induced non-GPVI signals was highlighted by the ability of U46619 and collagen to induce the secretion of ATP in FcRgamma chain-deficient platelets, even though neither agonist was effective alone. Protein tyrosine phosphorylation and the release of ATP were abolished by the anti-(alpha2 integrin) antibodies Ha1/29 and HMalpha2, but not by blockade of alphaIIbbeta3. These results illustrate a novel mechanism of platelet activation by collagen which is independent of the GPVI-FcRgamma chain complex, and is facilitated by binding of collagen to integrin alpha2beta1.
我们研究了胶原蛋白在缺乏FcRγ(Fc受体γ)链的小鼠血小板悬液中诱导信号传导和功能反应的能力,这些血小板缺乏胶原蛋白受体GPVI(糖蛋白VI)。在缺乏FcRγ链的情况下,胶原蛋白诱导了一种独特的酪氨酸磷酸化模式,血栓素类似物U46619可增强这种模式。免疫沉淀研究表明,单独的胶原蛋白或胶原蛋白加U46619的组合均未诱导GPVI调节蛋白Syk和SLP - 76(含Src同源2结构域的76 kDa白细胞蛋白)的磷酸化。观察到磷脂酶Cγ2有低水平的酪氨酸磷酸化,在U46619存在时增加,尽管磷酸化程度仍远低于野生型血小板中观察到的水平(约10%)。相比之下,衔接蛋白ADAP(促进黏附和解颗粒的衔接蛋白)的胶原蛋白诱导磷酸化被U46619显著增强至与野生型血小板中观察到的水平相当。胶原蛋白加U46619也诱导了粘着斑激酶(FAK)的显著磷酸化。U46619和胶原蛋白诱导FcRγ链缺陷血小板中ATP分泌的能力突出了胶原蛋白诱导的非GPVI信号的功能意义,尽管单独一种激动剂均无效。抗(α2整合素)抗体Ha1/29和HMα2可消除蛋白酪氨酸磷酸化和ATP释放,但阻断αIIbβ3则不能。这些结果说明了胶原蛋白激活血小板的一种新机制,该机制独立于GPVI - FcRγ链复合物,并且通过胶原蛋白与整合素α2β1的结合而促进。