Control of B-1a cell development by instructive BCR signaling

Curr Opin Immunol. 2018 Apr:51:24-31. doi: 10.1016/j.coi.2018.01.001. Epub 2018 Feb 3.

Abstract

B-1a cells remain one of the most enigmatic lymphocyte subsets. In this review, we discuss recent advances in our understanding of the development of these cells and their regulation by the transcription factors Bhlhe41 and Arid3a as well as by the RNA-binding protein Lin28b. A large body of literature supports an instructive role of BCR signaling in B-1a cell development and lineage commitment, which is initiated only after signaling from an autoreactive BCR. While both fetal and adult hematopoiesis can generate B-1a cells, the contribution of adult hematopoiesis to the B-1a cell compartment is low under physiological conditions. We discuss several models that can reconcile the instructive role of BCR signaling with this fetal bias in B-1a cell development.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • B-Lymphocyte Subsets / cytology*
  • B-Lymphocyte Subsets / immunology
  • B-Lymphocyte Subsets / metabolism*
  • Cell Differentiation* / genetics
  • Cell Differentiation* / immunology
  • Cell Lineage
  • Clonal Selection, Antigen-Mediated
  • Evolution, Molecular
  • Gene Expression Regulation, Developmental
  • Gene Rearrangement, B-Lymphocyte / genetics
  • Gene Rearrangement, B-Lymphocyte / immunology
  • Humans
  • Immunoglobulins / genetics
  • Receptors, Antigen, B-Cell / metabolism*
  • Signal Transduction*

Substances

  • IgK
  • Immunoglobulins
  • Receptors, Antigen, B-Cell