Faculty, Staff and Student Publications

Publication Date

8-1-2022

Journal

Molecular Immunology

Abstract

Plasmacytoid dendritic cells (pDCs) are specialized type I interferon (IFN-I) producing cells that promote anti-viral immune responses and contribute to autoimmunity. Development of pDCs requires the transcriptional regulator E2-2 and is opposed by inhibitor of DNA binding 2 (Id2). Prior work indicates Id2 is induced in pDCs upon maturation and may affect pDC IFN-I production via suppression of E2-2, suggesting an important yet uncharacterized role in this lineage. We found TLR7 agonists stimulate Id2 mRNA and protein expression in pDCs. We further show that transcriptional activation of Id2 is dependent on the E2 ubiquitin-conjugating enzyme Ubc13, but independent of IFN-I signaling in response to TLR7 agonist stimulation. Nonetheless, conditional Id2 depletion in pDCs indicates Id2 is dispensable for TLR7 agonist-induced maturation and inhibition of E2-2 expression. Thus, we identify new mechanisms of Id2 regulation by Ubc13, which may be relevant for understanding Id2 gene regulation in other contexts, while ruling out major roles for Id2 in pDC responses to TLR7 agonists.

Keywords

Dendritic Cells, Gene Expression Regulation, Interferon Type I, Toll-Like Receptor 7, IFNAR signaling, Id2, Soluble factors, TLR, Ubc13, pDCs

DOI

10.1016/j.molimm.2022.05.009

PMID

35640521

PMCID

PMC11390127

PubMedCentral® Posted Date

9-11-2024

PubMedCentral® Full Text Version

Author MSS

Published Open-Access

yes

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