4.6 Review Book Chapter

Regulation and functions of blimp-1 in T and B lymphocytes

Journal

ANNUAL REVIEW OF IMMUNOLOGY
Volume 26, Issue -, Pages 133-169

Publisher

ANNUAL REVIEWS
DOI: 10.1146/annurev.immunol.26.021607.090241

Keywords

transcription; repressor; terminal differentiation; cytokines

Categories

Funding

  1. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI043576] Funding Source: NIH RePORTER
  2. NIAID NIH HHS [R01AI43576, R01AI 50569] Funding Source: Medline

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B lymphocyte-induced maturation protein-1 (Blimp-1), discovered 16 years ago as a transcriptional repressor of the IFN beta promoter, plays fundamentally important roles in many cell lineages and in early development. This review focuses on Blimp-1 in lymphocytes. In the B cell lineage, Blimp-l is required for development of immunoglobulin-secreting cells and for maintenance of long-lived plasma cells (LLPCs). Direct targets of Blimp-1 and the transcriptional cascades Blimp-1 initiates to trigger plasmacytic differentiation are described. Blimp-1 also affects the homeostasis and function of CD4+, CD8+, and regulatory CD4+ T cells, and Blimp-1 levels are highest in antigen-experienced T cells. Blimp-1 attenuates T cell proliferation and survival and modulates differentiation. Roles for Blimp-1 in Th1/Th2 specification, regulatory T cell function, and CD8 differentiation and function ire under investigation. Signals that induce Blimp-1 in B cells include Toll-like receptor ligands and cytokines; in T cells, T cell receptors and cytokines induce Blimp-1. In spite of some commonalities, different targets and regulators of Blimp-1 in B and T cells suggest intriguing evolutionary divergence of this regulatory machinery.

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