| Literature DB >> 26527007 |
Jianbo Sun1, Jiguang Wang2, Evangelos Pefanis1, Jaime Chao1, Gerson Rothschild1, Isao Tachibana3, Jun Kui Chen1, Ivaylo I Ivanov1, Raul Rabadan2, Yoshito Takeda3, Uttiya Basu4.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26527007 PMCID: PMC4644501 DOI: 10.1016/j.celrep.2015.09.070
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423