Department of Clinical and Laboratory Medicine, Faculty of Medicine, University of Yamanashi, Chuo, Yamanashi, Japan.
J Thromb Haemost. 2011 Jul;9 Suppl 1:44-55. doi: 10.1111/j.1538-7836.2011.04335.x.
C-type lectin-like receptor 2 (CLEC-2) has been identified as a receptor for the platelet activating snake venom rhodocytin. CLEC-2 elicits powerful platelet activation signals in conjunction with Src, Syk kinases, and phospholipase Cγ2, similar to the collagen receptor glycoprotein (GP) VI/FcRγ-chain complex. In contrast to GPVI/FcRγ, which initiates platelet activation through the tandem YxxL motif immunoreceptor tyrosine-based activation motif (ITAM), CLEC-2 signals via the single YxxL motif hemi-ITAM. The endogenous ligand of CLEC-2 has been identified as podoplanin, which is expressed on the surface of tumour cells and facilitates tumour metastasis by inducing platelet activation. Studies of CLEC-2-deficient mice have revealed several physiological roles of CLEC-2. Podoplanin is also expressed in lymphatic endothelial cells as well as several other cells, including type I alveolar cells and kidney podocytes, but is absent from vascular endothelial cells. In the developmental stages, when the primary lymph sac is derived from the cardinal vein, podoplanin activates platelets in lymphatic endothelial cells by binding to CLEC-2, which facilitates blood/lymphatic vessel separation. Moreover, CLEC-2 is involved in thrombus stabilisation under flow conditions in part through homophilic interactions. However, the absence of CLEC-2 does not significantly increase bleeding tendency. CLEC-2 may be a good target protein for novel anti-platelet drugs or anti-metastatic drugs having therapeutic and preventive effects on arterial thrombosis and cancer, the primary causes of mortality in developed countries. In this article, we review the mechanisms of signal transduction, structure, expression, and function of CLEC-2.
C 型凝集素样受体 2(CLEC-2)已被鉴定为血小板激活蛇毒 rhodocytin 的受体。CLEC-2 与Src、Syk 激酶和磷酯酶 Cγ2 一起引发强大的血小板激活信号,类似于胶原受体糖蛋白(GP)VI/FcRγ 链复合物。与通过串联 YxxL 基序免疫受体酪氨酸激活基序(ITAM)启动血小板激活的 GPVI/FcRγ 不同,CLEC-2 通过单个 YxxL 基序半 ITAM 发出信号。CLEC-2 的内源性配体已被鉴定为 podoplanin,它表达在肿瘤细胞表面,通过诱导血小板激活促进肿瘤转移。CLEC-2 缺陷小鼠的研究揭示了 CLEC-2 的几种生理作用。Podoplanin 也在淋巴管内皮细胞以及其他几种细胞(包括 I 型肺泡细胞和肾脏足细胞)中表达,但不存在于血管内皮细胞中。在发育阶段,当初级淋巴囊从心静脉衍生时,podoplanin 通过与 CLEC-2 结合激活淋巴管内皮细胞中的血小板,从而促进血液/淋巴管分离。此外,CLEC-2 部分通过同型相互作用参与血流条件下的血栓稳定。然而,CLEC-2 的缺失并没有显著增加出血倾向。CLEC-2 可能是一种新型抗血小板药物或抗转移药物的良好靶蛋白,对发达国家死亡率的主要原因——动脉血栓形成和癌症具有治疗和预防作用。本文综述了 CLEC-2 的信号转导、结构、表达和功能的机制。