TY - JOUR
T1 - T Cells Regulate Peripheral Naive Mature B Cell Survival by Cell-Cell Contact Mediated through SLAMF6 and SAP
AU - Radomir, Lihi
AU - Cohen, Sivan
AU - Kramer, Matthias P.
AU - Bakos, Eszter
AU - Lewinsky, Hadas
AU - Barak, Avital
AU - Porat, Ziv
AU - Bucala, Richard
AU - Stepensky, Polina
AU - Becker-Herman, Shirly
AU - Shachar, Idit
N1 - Publisher Copyright: Copyright © 2017 by The American Association of Immunologists, Inc.
PY - 2017/10/15
Y1 - 2017/10/15
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85031508156&partnerID=8YFLogxK
U2 - 10.4049/jimmunol.1700557
DO - 10.4049/jimmunol.1700557
M3 - مقالة
SN - 0022-1767
VL - 199
SP - 2745
EP - 2757
JO - Journal of Immunology
JF - Journal of Immunology
IS - 8
ER -