Endogenous MHC-related protein 1 is transiently expressed on the plasma membrane in a conformation that activates mucosal-associated invariant T cells

The development of mucosal-associated invariant T (MAIT) cells is dependent upon the class Ib molecule MHC-related protein 1 (MR1), commensal bacteria, and a thymus. Furthermore, recent studies have implicated MR1 presentation to MAIT cells in bacteria recognition, although the mechanism remains und...

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Veröffentlicht in:The Journal of immunology (1950) 2011-04, Vol.186 (8), p.4744-4750
Hauptverfasser: Chua, Wei-Jen, Kim, Sojung, Myers, Nancy, Huang, Shouxiong, Yu, Lawrence, Fremont, Daved H, Diamond, Michael S, Hansen, Ted H
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container_end_page 4750
container_issue 8
container_start_page 4744
container_title The Journal of immunology (1950)
container_volume 186
creator Chua, Wei-Jen
Kim, Sojung
Myers, Nancy
Huang, Shouxiong
Yu, Lawrence
Fremont, Daved H
Diamond, Michael S
Hansen, Ted H
description The development of mucosal-associated invariant T (MAIT) cells is dependent upon the class Ib molecule MHC-related protein 1 (MR1), commensal bacteria, and a thymus. Furthermore, recent studies have implicated MR1 presentation to MAIT cells in bacteria recognition, although the mechanism remains undefined. Surprisingly, however, surface expression of MR1 has been difficult to detect serologically, despite ubiquitous detection of MR1 transcripts and intracellular protein. In this article, we define a unique mAb capable of stabilizing endogenous mouse MR1 at the cell surface, resulting in enhanced mouse MAIT cell activation. Our results demonstrated that under basal conditions, endogenous MR1 transiently visits the cell surface, thus reconciling the aforementioned serologic and functional studies. Furthermore, using this approach, double-positive thymocytes, macrophages, and dendritic cells were identified as potential APCs for MAIT cell development and activation. Based on this pattern of MR1 expression, it is intriguing to speculate that constitutive expression of MR1 may be detrimental for maintenance of immune homeostasis in the gut and/or detection of pathogenic bacteria in mucosal tissues.
doi_str_mv 10.4049/jimmunol.1003254
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subjects Animals
Antibodies, Monoclonal - immunology
Antibodies, Monoclonal - metabolism
B-Lymphocytes - immunology
B-Lymphocytes - metabolism
Cattle
Cell Membrane - immunology
Cell Membrane - metabolism
Cross Reactions - immunology
Dendritic Cells - immunology
Dendritic Cells - metabolism
Epitopes - immunology
Epitopes - metabolism
Flow Cytometry
Histocompatibility Antigens Class I - genetics
Histocompatibility Antigens Class I - immunology
Histocompatibility Antigens Class I - metabolism
Humans
Hybridomas - immunology
Lymphocyte Activation - immunology
Macrophages - immunology
Macrophages - metabolism
Mice
Mice, Inbred C57BL
Mice, Knockout
Minor Histocompatibility Antigens
Mucous Membrane - cytology
Mucous Membrane - immunology
Mucous Membrane - metabolism
Protein Binding
Rats
T-Lymphocytes - immunology
T-Lymphocytes - metabolism
Thymus Gland - cytology
Thymus Gland - immunology
Thymus Gland - metabolism
title Endogenous MHC-related protein 1 is transiently expressed on the plasma membrane in a conformation that activates mucosal-associated invariant T cells
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