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黏附与脱颗粒促进衔接蛋白在整合素α2β1介导的胶原诱导的血小板激活中的作用。

A role for adhesion and degranulation-promoting adapter protein in collagen-induced platelet activation mediated via integrin α(2) β(1).

机构信息

School of Pharmacy, Queen's University Belfast, Belfast, UK.

出版信息

J Thromb Haemost. 2012 Feb;10(2):268-77. doi: 10.1111/j.1538-7836.2011.04567.x.

Abstract

BACKGROUND

Collagen-induced platelet activation is a key step in the development of arterial thrombosis via its interaction with the receptors glycoprotein (GP)VI and integrin α(2) β(1) . Adhesion and degranulation-promoting adapter protein (ADAP) regulates α(IIb) β(3) in platelets and α(L) β(2) in T cells, and is phosphorylated in GPVI-deficient platelets activated by collagen.

OBJECTIVES

To determine whether ADAP plays a role in collagen-induced platelet activation and in the regulation and function of α(2) β(1).

METHODS

Using ADAP(-/-) mice and synthetic collagen peptides, we investigated the role of ADAP in platelet aggregation, adhesion, spreading, thromboxane synthesis, and tyrosine phosphorylation.

RESULTS AND CONCLUSIONS

Platelet aggregation and phosphorylation of phospholipase Cγ2 induced by collagen were attenuated in ADAP(-/-) platelets. However, aggregation and signaling induced by collagen-related peptide (CRP), a GPVI-selective agonist, were largely unaffected. Platelet adhesion to CRP was also unaffected by ADAP deficiency. Adhesion to the α(2) β(1) -selective ligand GFOGER and to a peptide (III-04), which supports adhesion that is dependent on both GPVI and α(2) β(1), was reduced in ADAP(-/-) platelets. An impedance-based label-free detection technique, which measures adhesion and spreading of platelets, indicated that, in the absence of ADAP, spreading on GFOGER was also reduced. This was confirmed with non-fluorescent differential-interference contrast microscopy, which revealed reduced filpodia formation in ADAP(-/-) platelets adherent to GFOGER. This indicates that ADAP plays a role in mediating platelet activation via the collagen-binding integrin α(2) β(1). In addition, we found that ADAP(-/-) mice, which are mildly thrombocytopenic, have enlarged spleens as compared with wild-type animals. This may reflect increased removal of platelets from the circulation.

摘要

背景

胶原蛋白诱导的血小板激活是通过与糖蛋白 (GP)VI 和整合素 α(2)β(1) 受体相互作用在动脉血栓形成中发挥关键作用的。衔接蛋白和促脱颗粒适配器蛋白(ADAP)调节血小板中的 α(IIb)β(3) 和 T 细胞中的 α(L)β(2),并且在由胶原蛋白激活的 GPVI 缺陷型血小板中被磷酸化。

目的

确定 ADAP 是否在胶原蛋白诱导的血小板激活以及 α(2)β(1) 的调节和功能中发挥作用。

方法

使用 ADAP(-/-) 小鼠和合成胶原蛋白肽,我们研究了 ADAP 在血小板聚集、黏附、伸展、血栓烷合成和酪氨酸磷酸化中的作用。

结果与结论

胶原蛋白诱导的血小板聚集和磷脂酶 Cγ2 的磷酸化在 ADAP(-/-) 血小板中减弱。然而,由胶原蛋白相关肽 (CRP) 诱导的聚集和信号转导,一种 GPVI 选择性激动剂,受 ADAP 缺乏的影响很小。血小板对 CRP 的黏附也不受 ADAP 缺乏的影响。对 α(2)β(1) 选择性配体 GFOGER 和支持依赖于 GPVI 和 α(2)β(1) 的黏附的肽 (III-04) 的黏附在 ADAP(-/-) 血小板中减少。基于阻抗的无标记检测技术测量血小板的黏附和伸展,表明在缺乏 ADAP 的情况下,GFOGER 上的伸展也减少。这通过非荧光差示干涉对比显微镜得到证实,该显微镜显示 ADAP(-/-) 血小板在 GFOGER 上的伪足形成减少。这表明 ADAP 在介导通过胶原蛋白结合整合素 α(2)β(1) 的血小板激活中发挥作用。此外,我们发现与野生型动物相比,轻度血小板减少的 ADAP(-/-) 小鼠的脾脏增大。这可能反映了血小板从循环中被清除增加。

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