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2B4:一种具有独特特异性和信号转导机制的自然杀伤细胞激活受体。

2B4: an NK cell activating receptor with unique specificity and signal transduction mechanism.

作者信息

Nakajima H, Colonna M

机构信息

Basel Institute for Immunology, Switzerland.

出版信息

Hum Immunol. 2000 Jan;61(1):39-43. doi: 10.1016/s0198-8859(99)00170-6.

Abstract

2B4 is a cell surface glycoprotein of the Ig-superfamily structurally related to CD2-like molecules such as CD2, CD48, CD58, CD84, Ly-9, and SLAM. Engagement of 2B4 on NK cells with specific antibodies or with its ligand CD48 enhances NK cell-mediated cytotoxicity. 2B4 is also expressed on both CD8+ T cells and myeloid cells, but its function in these cells remains unknown. Signal transduction through 2B4 involves recruitment of the SH2-containing adapter molecule SAP to cytoplasmic tyrosines. SAP is deficient in patients affected by X-linked lymphoproliferative disorder (XLP), which is triggered following EBV infection. Thus, an interruption of signaling through 2B4 and related molecules may impair NK cell recognition of virally infected cells and contribute to XLP.

摘要

2B4是免疫球蛋白超家族的一种细胞表面糖蛋白,在结构上与CD2样分子相关,如CD2、CD48、CD58、CD84、Ly-9和信号淋巴细胞激活分子(SLAM)。用特异性抗体或其配体CD48作用于自然杀伤(NK)细胞上的2B4,可增强NK细胞介导的细胞毒性。2B4在CD8 + T细胞和髓样细胞上也有表达,但其在这些细胞中的功能尚不清楚。通过2B4的信号转导涉及含Src同源2(SH2)结构域的衔接分子信号淋巴细胞激活分子相关蛋白(SAP)募集到细胞质酪氨酸。在受X连锁淋巴增生性疾病(XLP)影响的患者中,SAP是缺陷的,该病是由EB病毒感染引发的。因此,通过2B4和相关分子的信号传导中断可能会损害NK细胞对病毒感染细胞的识别,并导致XLP。

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