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Cutting Edge: Endogenous IFN-ß Regulates Survival and Development of Transitional B Cells.
Hamilton, Jennie A; Wu, Qi; Yang, PingAr; Luo, Bao; Liu, Shanrun; Hong, Huixian; Li, Jun; Walter, Mark R; Fish, Eleanor N; Hsu, Hui-Chen; Mountz, John D.
Afiliación
  • Hamilton JA; Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294.
  • Wu Q; Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294.
  • Yang P; Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294.
  • Luo B; Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294.
  • Liu S; Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294.
  • Hong H; Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294.
  • Li J; Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294.
  • Walter MR; Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294.
  • Fish EN; Toronto General Research Institute, University Health Network, Toronto, Ontario M5G 2C4, Canada.
  • Hsu HC; Department of Immunology, University of Toronto, Toronto, Ontario M5G 2M1, Canada; and.
  • Mountz JD; Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294.
J Immunol ; 199(8): 2618-2623, 2017 10 15.
Article en En | MEDLINE | ID: mdl-28904124
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-ß 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-ß. 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-ß plays a key role in regulating responsiveness to external factors.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bazo / Nefritis Lúpica / Linfocitos B / Interferón beta / Células Precursoras de Linfocitos B Límite: Animals Idioma: En Revista: J Immunol Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Bazo / Nefritis Lúpica / Linfocitos B / Interferón beta / Células Precursoras de Linfocitos B Límite: Animals Idioma: En Revista: J Immunol Año: 2017 Tipo del documento: Article