The Transcription Factor RORα Preserves ILC3 Lineage Identity and Function during Chronic Intestinal Infection
Author(s) -
Bernard C. Lo,
Diana Canals Hernaez,
R. Wilder Scott,
Michael R. Hughes,
Samuel B. Shin,
T. Michael Underhill,
Fumio Takei,
Kelly M. McNagny
Publication year - 2019
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1900781
Subject(s) - rar related orphan receptor gamma , innate lymphoid cell , transcription factor , orphan receptor , biology , immunology , sox9 , microbiology and biotechnology , cancer research , immunity , immune system , gene , genetics
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 tha Rora sg/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 Rora sg/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.
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