N6-Methyladenosine Directly Regulates CD40L Expression in CD4+ T Lymphocytes

Author:

van Vroonhoven Ellen C. N.1ORCID,Picavet Lucas W.1,Scholman Rianne C.1,van den Dungen Noortje A. M.2,Mokry Michal2,Evers Anouk3,Lebbink Robert J.3ORCID,Calis Jorg J. A.1,Vastert Sebastiaan J.14,van Loosdregt Jorg1

Affiliation:

1. Center for Translational Immunology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands

2. Department of Experimental Cardiology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands

3. Department of Medical Microbiology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands

4. Department of Pediatric Rheumatology and Immunology, University Medical Center Utrecht, 3584 CX Utrecht, The Netherlands

Abstract

T cell activation is a highly regulated process, modulated via the expression of various immune regulatory proteins including cytokines, surface receptors and co-stimulatory proteins. N6-methyladenosine (m6A) is an RNA modification that can directly regulate RNA expression levels and it is associated with various biological processes. However, the function of m6A in T cell activation remains incompletely understood. We identify m6A as a novel regulator of the expression of the CD40 ligand (CD40L) in human CD4+ lymphocytes. Manipulation of the m6A ‘eraser’ fat mass and obesity-associated protein (FTO) and m6A ‘writer’ protein methyltransferase-like 3 (METTL3) directly affects the expression of CD40L. The m6A ‘reader’ protein YT521-B homology domain family-2 (YTHDF2) is hypothesized to be able to recognize and bind m6A specific sequences on the CD40L mRNA and promotes its degradation. This study demonstrates that CD40L expression in human primary CD4+ T lymphocytes is regulated via m6A modifications, elucidating a new regulatory mechanism in CD4+ T cell activation that could possibly be leveraged in the future to modulate T cell responses in patients with immune-related diseases.

Funder

Dutch Arthritis Foundation

Publisher

MDPI AG

Subject

General Agricultural and Biological Sciences,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology

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