Radomir Lihi, Cohen Sivan, Kramer Matthias P, Bakos Eszter, Lewinsky Hadas, Barak Avital, Porat Ziv, Bucala Richard, Stepensky Polina, Becker-Herman Shirly, Shachar Idit
Department of Immunology, Weizmann Institute of Science, Rehovot 76100, Israel.
Department of Biological Services, Weizmann Institute of Science, Rehovot 76100, Israel.
J Immunol. 2017 Oct 15;199(8):2745-2757. doi: 10.4049/jimmunol.1700557. Epub 2017 Sep 13.
The control of lymphoid homeostasis is the result of a very fine balance between lymphocyte production, proliferation, and apoptosis. In this study, we focused on the role of T cells in the maintenance/survival of the mature naive peripheral B cell population. We show that naive B and T cells interact via the signaling lymphocyte activation molecule (SLAM) family receptor, SLAMF6. This interaction induces cell type-specific signals in both cell types, mediated by the SLAM-associated protein (SAP) family of adaptors. This signaling results in an upregulation of the expression of the cytokine migration inhibitory factor in the T cells and augmented expression of its receptor CD74 on the B cell counterparts, consequently enhancing B cell survival. Furthermore, in X-linked lymphoproliferative disease patients, SAP deficiency reduces CD74 expression, resulting in the perturbation of B cell maintenance from the naive stage. Thus, naive T cells regulate B cell survival in a SLAMF6- and SAP-dependent manner.
淋巴细胞稳态的控制是淋巴细胞生成、增殖和凋亡之间非常精细平衡的结果。在本研究中,我们聚焦于T细胞在成熟幼稚外周B细胞群体维持/存活中的作用。我们发现幼稚B细胞和T细胞通过信号淋巴细胞激活分子(SLAM)家族受体SLAMF6相互作用。这种相互作用在两种细胞类型中诱导细胞类型特异性信号,由衔接蛋白的SLAM相关蛋白(SAP)家族介导。该信号传导导致T细胞中细胞因子迁移抑制因子表达上调,其在B细胞对应物上的受体CD74表达增加,从而提高B细胞存活率。此外,在X连锁淋巴增生性疾病患者中,SAP缺乏会降低CD74表达,导致幼稚阶段B细胞维持受到干扰。因此,幼稚T细胞以SLAMF6和SAP依赖的方式调节B细胞存活。