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The Transcription Factor RORα Preserves ILC3 Lineage Identity and Function during Chronic Intestinal Infection.

Authors :
Lo, Bernard C.
Canals Hernaez, Diana
Scott, R. Wilder
Hughes, Michael R.
Shin, Samuel B.
Underhill, T. Michael
Fumio Takei
McNagny, Kelly M.
Source :
Journal of Immunology. 12/15/2019, Vol. 203 Issue 12, p3209-3215. 7p.
Publication Year :
2019

Abstract

Innate lymphoid cells (ILCs) are critical for host defense and tissue repair but can also contribute to chronic inflammatory diseases. The transcription factor RORα is required for ILC2 development but is also highly expressed by other ILC subsets where its function remains poorly defined. We previously reported that Rorasg/sg bone marrow chimeric mice (C57BL/6J) were protected from Salmonella-induced intestinal fibrosis due to defective ILC3 responses. In this study, single-cell RNA analysis of ILCs isolated from inflamed tissues indicates that RORα perturbation led to a reduction in ILC3 lineages. Furthermore, residual Rorasg/sg ILC3s have decreased expression of key signature genes, including Rorc and activating cytokine receptors. Collectively, our data suggest that RORα plays a key role in preserving functional ILC3s by modulating their ability to integrate environmental cues to efficiently produce cytokines. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221767
Volume :
203
Issue :
12
Database :
Academic Search Index
Journal :
Journal of Immunology
Publication Type :
Academic Journal
Accession number :
140385605
Full Text :
https://doi.org/10.4049/jimmunol.1900781