Regulatory B cells (Breg) have immune suppressive functions in various autoimmune/inflammation models and diseases and are found to be enriched in diverse B cell subsets. The lack of a unique marker or set of markers efficiently identifying Breg cells impedes detailed investigation into their origin, development, and immunological roles. Here, we perform transcriptome analysis of IL-10-expressing B cells to identify key regulators for Breg biogenesis and function and identify CD9, a tetraspanin-family transmembrane protein, as a key surface marker for most mouse IL-10(+) B cells and their progenitors. CD9 plays a role in the suppressive function of IL-10(+) B cells in ex vivo T cell proliferation assays through a mechanism that is dependent upon B/T cell interactions. CD9(+) B cells also demonstrate inhibition of Th1-mediated contact hypersensitivity in an in vivo model system. Taken together, our findings implicate CD9 in the immunosuppressive activity of regulatory B cells.
Transcriptomics Identify CD9 as a Marker of Murine IL-10-Competent Regulatory B Cells.
Jianbo Sun,Jiguang Wang,Evangelos Pefanis,Jaime L. Chao,Gerson Rothschild,I. Tachibana,Jun Kui Chen,I. Ivanov,R. Rabadán,Y. Takeda,Uttiya Basu
Published 2015 in Cell Reports
ABSTRACT
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- Publication year
2015
- Venue
Cell Reports
- Publication date
2015-11-10
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
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