Please use this identifier to cite or link to this item: https://doi.org/10.3390/cells10020353
Title: Regulatory t cells inhibit t cell activity by downregulating cd137 ligand via cd137 trogocytosis
Authors: Luu, Khang
Patwardhan, Mugdha Vijay
Zeng, Qun 
Wickström, S.L.
Lundqvist, Andreas
Schwarz, Herbert 
Keywords: CD137
Regulatory T cells
Trogocytosis
Issue Date: 9-Feb-2021
Publisher: MDPI
Citation: Luu, Khang, Patwardhan, Mugdha Vijay, Zeng, Qun, Wickström, S.L., Lundqvist, Andreas, Schwarz, Herbert (2021-02-09). Regulatory t cells inhibit t cell activity by downregulating cd137 ligand via cd137 trogocytosis. Cells 10 (2) : 1-Nov. ScholarBank@NUS Repository. https://doi.org/10.3390/cells10020353
Rights: Attribution 4.0 International
Abstract: CD137 is a costimulatory molecule expressed on activated T cells. CD137 ligand (CD137L) is expressed by antigen presenting cells (APC), which use the CD137—CD137L system to enhance immune responses. It was, therefore, surprising to discover CD137 expression on regulatory T cells (Treg). The function of CD137 in Treg are controversial. While some studies report that CD137 signalling converts Treg to effector T cells (Teff), other studies find that CD137-expressing Treg display a stronger inhibitory activity than CD137- Treg. Here, we describe that CD137 on Treg binds to CD137L on APC, upon which one of the two molecules is transferred via trogocytosis to the other cell, where CD137—CD137L forms a complex that is internalized and deprives APC of the immune-stimulatory CD137L. Truncated forms of CD137 that lack the cytoplasmic domain of CD137 are also able to downregulate CD137L, demonstrating that CD137 signalling is not required. Comparable data have been obtained with human and murine cells, indicating that this mechanism is evolution-arily conserved. These data describe trogocytosis of CD137 and CD137L as a new mechanism em-ployed by Treg to control immune responses by downregulating the immunostimulatory CD137L on APC. © 2021 by the authors. Licensee MDPI, Basel, Switzerland.
Source Title: Cells
URI: https://scholarbank.nus.edu.sg/handle/10635/232143
ISSN: 2073-4409
DOI: 10.3390/cells10020353
Rights: Attribution 4.0 International
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