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NKG2D招募两种不同的衔接蛋白以触发自然杀伤细胞的激活和共刺激。

NKG2D recruits two distinct adapters to trigger NK cell activation and costimulation.

作者信息

Gilfillan Susan, Ho Emily L, Cella Marina, Yokoyama Wayne M, Colonna Marco

机构信息

Department of Pathology and Immunology, Washington University School of Medicine, 660 S. Euclid, St. Louis, MO 63110, USA.

出版信息

Nat Immunol. 2002 Dec;3(12):1150-5. doi: 10.1038/ni857. Epub 2002 Nov 11.

Abstract

NKG2D is a receptor on natural killer (NK) cells and cytotoxic T lymphocytes that binds major histocompatibility complex (MHC) class I-like ligands expressed primarily on virally infected and neoplastic cells. In vitro studies indicate that NKG2D provides costimulation through an associated adapter, DAP10, which recruits phosphatidylinositol-3 kinase. Here we show that in DAP10-deficient mice, CD8+ T cells lack NKG2D expression and are incapable of mounting tumor-specific responses. However, DAP10-deficient NK cells express a functional NKG2D receptor due to the association of NKG2D with another adapter molecule, DAP12 (also known as KARAP), which recruits protein tyrosine kinases. Thus, NKG2D is a versatile receptor that, depending on the availability of adapter partners, mediates costimulation in T cells and/or activation in NK cells.

摘要

NKG2D是自然杀伤(NK)细胞和细胞毒性T淋巴细胞上的一种受体,它能与主要组织相容性复合体(MHC)I类样配体结合,这些配体主要表达于病毒感染细胞和肿瘤细胞上。体外研究表明,NKG2D通过相关衔接蛋白DAP10提供共刺激,DAP10可募集磷脂酰肌醇-3激酶。我们在此表明,在缺乏DAP10的小鼠中,CD8 + T细胞缺乏NKG2D表达,无法产生肿瘤特异性反应。然而,由于NKG2D与另一种衔接分子DAP12(也称为KARAP)结合,缺乏DAP10的NK细胞表达功能性NKG2D受体,DAP12可募集蛋白酪氨酸激酶。因此,NKG2D是一种多功能受体,根据衔接蛋白伙伴的可用性,它可介导T细胞中的共刺激和/或NK细胞中的激活。

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