Cutting Edge: Endogenous IFN-β Regulates Survival and Development of Transitional B Cells
Author(s) -
Jennie A Hamilton,
Qi Wu,
PingAr Yang,
Bao Luo,
Shanrun Liu,
Huixian Hong,
Jun Li,
Mark R. Walter,
Eleanor N. Fish,
HuiChen Hsu,
John D. Mountz
Publication year - 2017
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.1700888
Subject(s) - biology , b cell , tlr7 , downregulation and upregulation , microbiology and biotechnology , endogeny , spleen , immune system , immunology , gene , genetics , antibody , innate immune system , toll like receptor , endocrinology
The transitional stage of B cell development is a formative stage in the spleen where autoreactive specificities are censored as B cells gain immune competence, but the intrinsic and extrinsic factors regulating survival of transitional stage 1 (T1) B cells are unknown. We report that B cell expression of IFN-β is required for optimal survival and TLR7 responses of transitional B cells in the spleen and was overexpressed in T1 B cells from BXD2 lupus-prone mice. Single-cell gene expression analysis of B6 Ifnb +/+ versus B6 Ifnb -⁄- T1 B cells revealed heterogeneous expression of Ifnb in wild-type B cells and distinct gene expression patterns associated with endogenous IFN-β. Single-cell analysis of BXD2 T1 B cells revealed that Ifnb is expressed in early T1 B cell development with subsequent upregulation of Tlr7 and Ifna1 Together, these data suggest that T1 B cell expression of IFN-β plays a key role in regulating responsiveness to external factors.
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