An inducible circular RNA circKcnt2 inhibits ILC3 activation to facilitate colitis resolution. Academic Article uri icon

Overview

abstract

  • Group 3 innate lymphoid cells (ILC3) are an important regulator for immunity, inflammation and tissue homeostasis in the intestine, but how ILC3 activation is regulated remains elusive. Here we identify a new circular RNA (circRNA) circKcnt2 that is induced in ILC3s during intestinal inflammation. Deletion of circKcnt2 causes gut ILC3 activation and severe colitis in mice. Mechanistically, circKcnt2, as a nuclear circRNA, recruits the nucleosome remodeling deacetylase (NuRD) complex onto Batf promoter to inhibit Batf expression; this in turn suppresses Il17 expression and thereby ILC3 inactivation to promote innate colitis resolution. Furthermore, Mbd3-/-Rag1-/- and circKcnt2-/-Rag1-/- mice develop severe innate colitis following dextran sodium sulfate (DSS) treatments, while simultaneous deletion of Batf promotes colitis resolution. In summary, our data support a function of the circRNA circKcnt2 in regulating ILC3 inactivation and resolution of innate colitis.

publication date

  • August 14, 2020

Research

keywords

  • Colitis
  • Lymphocytes
  • Potassium Channels, Sodium-Activated
  • RNA, Circular

Identity

PubMed Central ID

  • PMC7427797

Scopus Document Identifier

  • 85089361078

Digital Object Identifier (DOI)

  • 10.1038/s41467-020-17944-5

PubMed ID

  • 32796851

Additional Document Info

volume

  • 11

issue

  • 1