| Literature DB >> 28904129 |
Lihi Radomir1, Sivan Cohen1, Matthias P Kramer1, Eszter Bakos1, Hadas Lewinsky1, Avital Barak1, Ziv Porat2, Richard Bucala3, Polina Stepensky4, Shirly Becker-Herman1, Idit Shachar5.
Abstract
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.Entities:
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Year: 2017 PMID: 28904129 PMCID: PMC5805483 DOI: 10.4049/jimmunol.1700557
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422