Characterization of marginal zone B cell precursors

J Exp Med. 2005 Nov 7;202(9):1225-34. doi: 10.1084/jem.20051038. Epub 2005 Oct 31.

Abstract

Selection of recently formed B cells into the follicular or marginal zone (MZ) compartments is proposed to occur by way of proliferative intermediates expressing high levels of CD21/35 and CD23. However, we show that CD21/35(high) CD23(+) splenocytes are not enriched for proliferative cells, and do not contribute substantially to the generation of follicular B cells. Instead, ontogenic relationships, steady-state labeling kinetics, and adoptive transfer experiments suggest that CD21/35(high) CD23(+) splenocytes serve primarily as precursors for MZ B cells, although their developmental potential seems to be broader and is influenced by environmental cues that are associated with lymphopenia. Furthermore, CD21/35(high) CD23(+) splenocytes share several key functional characteristics with MZ B cells, including their capacity to trap T-independent antigen and a heightened proliferative response to LPS. These observations challenge previous models of peripheral B cell maturation, and suggest that MZ B cells develop by way of CD21/35(high) CD23(+) intermediates.

Publication types

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

MeSH terms

  • Animals
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism
  • Bromodeoxyuridine / metabolism
  • Cell Differentiation / immunology*
  • Cell Proliferation
  • Cells, Cultured
  • Kinetics
  • Membrane Glycoproteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, Complement / metabolism
  • Receptors, Complement 3b / metabolism
  • Receptors, Complement 3d / metabolism
  • Receptors, IgE / metabolism
  • Spleen / cytology
  • Spleen / immunology
  • Spleen / metabolism
  • Stem Cells / metabolism
  • Stem Cells / physiology*

Substances

  • Membrane Glycoproteins
  • Receptors, Complement
  • Receptors, Complement 3b
  • Receptors, Complement 3d
  • Receptors, IgE
  • complement 1q receptor
  • Bromodeoxyuridine