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.

Original languageEnglish
Article number1004
Number of pages11
JournalBiology
Volume12
Issue number7
DOIs
Publication statusPublished - Jul 2023

Keywords

  • adaptive immunity
  • autoimmunity
  • CD40 ligand
  • epitranscriptomics
  • RNA methylation
  • T cell activation

Fingerprint

Dive into the research topics of 'N6-Methyladenosine Directly Regulates CD40L Expression in CD4+ T Lymphocytes'. Together they form a unique fingerprint.

Cite this