miR-155 promotes T reg cell development by safeguarding medullary thymic epithelial cell maturation

Author:

Dong Jiayi1ORCID,Warner Lindsey M.1ORCID,Lin Ling-Li1ORCID,Chen Mei-Chi1ORCID,O'Connell Ryan M.2ORCID,Lu Li-Fan134ORCID

Affiliation:

1. Division of Biological Sciences, University of California, San Diego, La Jolla, CA

2. Huntsman Cancer Institute and the Division of Microbiology and Immunology, Department of Pathology, University of Utah, Salt Lake City, UT

3. Moores Cancer Center, University of California, San Diego, La Jolla, CA

4. Center for Microbiome Innovation, University of California, San Diego, La Jolla, CA

Abstract

During thymocyte development, medullary thymic epithelial cells (mTECs) provide appropriate instructive cues in the thymic microenvironment for not only negative selection but also the generation of regulatory T (T reg) cells. Here, we identify that miR-155, a microRNA whose expression in T reg cells has previously been shown to be crucial for their development and homeostasis, also contributes to thymic T reg (tT reg) cell differentiation by promoting mTEC maturation. Mechanistically, we show that RANKL stimulation induces expression of miR-155 to safeguard the thymic medulla through targeting multiple known and previously uncharacterized molecules within the TGFβ signaling pathway, which is recognized for its role in restricting the maturation and expansion of mTECs. Our work uncovers a miR-155–TGFβ axis in the thymic medulla to determine mTEC maturity and, consequently, the quantity of tT reg cells and suggests that miR-155 ensures proper tT reg cell development in both cell-intrinsic and -extrinsic manners.

Funder

National Institutes of Health

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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