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Cell Rep. 2019 Mar 5;26(10):2681-2691.e5. doi: 10.1016/j.celrep.2019.02.024.

Fcμ receptor as a Costimulatory Molecule for T Cells.

Author information

1
Department of Immunology, Institute for Biomedical Aging Research, University of Innsbruck, 6020 Innsbruck, Austria. Electronic address: andreas.meryk@uibk.ac.at.
2
Department of Immunology, Institute for Biomedical Aging Research, University of Innsbruck, 6020 Innsbruck, Austria.
3
Division of Translational Cell Genetics, Medical University of Innsbruck, 6020 Innsbruck, Austria.
4
Department of Medical Epidemiology and Biostatistics, Karolinska Institute, 17177 Stockholm, Sweden.
5
Faculty of Medicine and Life Sciences, University of Tampere, Tampere 33014, Finland.
6
Department of Orthopedic Surgery, Hospital Wels-Grieskirchen, 4600 Wels, Austria.

Abstract

Fc receptor for IgM (FcμR)-deficient mice display dysregulated function of neutrophils, dendritic cells, and B cells. The relevance of FcμR to human T cells is still unknown. We show that FcμR is mostly stored inside the cell and that surface expression is tightly regulated. Decreased surface expression on T cells from elderly individuals is associated with alterations in the methylation pattern of the FCMR gene. Binding and internalization of IgM stimulate transport of FcμR to the cell surface to ensure sustained IgM uptake. Concurrently, IgM accumulates within the cell, and the surface expression of other receptors increases, among them the T cell receptor (TCR) and costimulatory molecules. This leads to enhanced TCR signaling, proliferation, and cytokine release, in response to low, but not high, doses of antigen. Our findings indicate that FcμR is an important regulator of T cell function and reveal an additional mode of interaction between B and T cells.

KEYWORDS:

FcμR; IgM; T cells; TCR activation

PMID:
30840890
DOI:
10.1016/j.celrep.2019.02.024
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