Immunofluorescence analysis of B-1 cell ontogeny in the mouse

Int Immunol. 1994 Mar;6(3):355-61. doi: 10.1093/intimm/6.3.355.

Abstract

In order to further understand the developmental aspects of B-1 cells, we characterized the ontogeny of this B cell population in the spleen and peritoneal cavity of BALB/c mice. Although there are B-1 cells in the spleen within the first 1-3 weeks after birth, they do not at any stage represent the majority of splenic B cells. Splenic B-1 cells reach peak levels at approximately 9 days after birth. The mesenteric lining that covers the small intestine of 7-day-old mice contains a population of IgM+ B cells, while at the same age, there are few lymphoid cells in the peritoneal cavity. Between 7 and 8 days after birth there is an influx of B cells into the peritoneal cavity. At 8 days, the first detectable peritoneal B cells appear to be of the B-1 type based on expression of IL-5 receptor and CD5. However, these peritoneal B-1 cells do not express Mac-1. This antigen is not expressed by the majority of peritoneal B-1 cells until 3 weeks. This study indicates that the majority of early splenic B cells are not B-1 cells and it suggests that the mesenteric tissues surrounding the gut contain B lymphocytes which traffic into the peritoneal cavity where they then reside.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Aging / immunology
  • Animals
  • Animals, Newborn / immunology
  • Antibodies, Monoclonal
  • Antigens, CD / biosynthesis
  • B-Lymphocyte Subsets / immunology*
  • CD5 Antigens
  • Fluorescent Antibody Technique
  • Immunoglobulin M / analysis
  • Macrophage-1 Antigen / biosynthesis
  • Mesentery / cytology*
  • Mesentery / growth & development
  • Mice
  • Mice, Inbred BALB C
  • Peritoneal Cavity / cytology*
  • Peritoneal Cavity / growth & development
  • Peritoneal Lavage
  • Receptors, Interleukin / biosynthesis
  • Receptors, Interleukin-5
  • Spleen / cytology*
  • Spleen / growth & development

Substances

  • Antibodies, Monoclonal
  • Antigens, CD
  • CD5 Antigens
  • Immunoglobulin M
  • Macrophage-1 Antigen
  • Receptors, Interleukin
  • Receptors, Interleukin-5