Boles K S, Stepp S E, Bennett M, Kumar V, Mathew P A
Department of Molecular Biology and Immunology and Institute for Cancer Research, University of North Texas Health Science Center, Fort Worth 76107-2699, USA.
Immunol Rev. 2001 Jun;181:234-49. doi: 10.1034/j.1600-065x.2001.1810120.x.
2B4 is a member of the CD2 subset of the immunoglobulin superfamily molecules expressed on natural killer (NK) cells and other leukocytes. It is the high affinity ligand for CD48. Engagement of 2B4 on NK-cell surfaces with specific antibodies or CD48 can trigger cell-mediated cytotoxicity, interferon-gamma secretion, phosphoinositol turnover and NK-cell invasiveness. The function of 2B4 in CD8+ T cells and myeloid cells remains unknown. The cytoplasmic domain of 2B4 contains unique tyrosine motifs (TxYxxV/I) that associate with src homology 2 domain-containing protein or signaling lymphocyte activation molecule (SLAM)-associated protein, whose mutation is the underlying genetic defect in the X-linked lymphoproliferative disease (XLPD). Impaired signaling via 2B4 and SLAM is implicated in the immunopathogenesis of XLPD. CS1 is a novel member of the CD2 subset that contains two of the unique tyrosine motifs present in 2B4 and SLAM. Signaling through 2B4, CS1 and other members of the CD2 subset may play a major role in the regulation of NK cells and other leukocyte functions.
2B4是免疫球蛋白超家族分子CD2亚群的成员,在自然杀伤(NK)细胞和其他白细胞上表达。它是CD48的高亲和力配体。用特异性抗体或CD48使NK细胞表面的2B4结合,可触发细胞介导的细胞毒性、γ干扰素分泌、磷酸肌醇周转和NK细胞侵袭性。2B4在CD8 + T细胞和髓样细胞中的功能尚不清楚。2B4的胞质结构域含有独特的酪氨酸基序(TxYxxV/I),这些基序与含src同源2结构域的蛋白或信号淋巴细胞激活分子(SLAM)相关蛋白相关联,其突变是X连锁淋巴增殖性疾病(XLPD)的潜在遗传缺陷。通过2B4和SLAM的信号传导受损与XLPD的免疫发病机制有关。CS1是CD2亚群的一个新成员,含有2B4和SLAM中存在的两个独特酪氨酸基序。通过2B4、CS1和CD2亚群的其他成员进行信号传导可能在NK细胞和其他白细胞功能的调节中起主要作用。