Peritoneal CD5+ B-1 cells have signaling properties similar to tolerant B cells

J Biol Chem. 2002 Aug 23;277(34):30707-15. doi: 10.1074/jbc.M202460200. Epub 2002 Jun 17.

Abstract

CD5(+) B (or B-1) cells are the normal precursors of B cell chronic lymphocytic leukemia. They differ from conventional B (B-2) cells with respect to their phenotype and mitogenic responses and are often secretors of the natural polyreactive antibodies in the serum. The origin of B-1 cells remains controversial, and the relationship between B-1 cells and autoreactive B cells is unclear. Here, we compare the signaling pathways that are activated by the engagement of the B cell antigen receptor (BCR) in B-1 and B-2 cells. Stimulation of the BCR leads to the induced activation of the three major classes of mitogen-activated protein kinases (MAPKs), ERK, JNK, and p38 MAPK, as well as the Akt kinase and the transcription factors nuclear factor of activated T cells (NF-AT) and NF-kappaB in B-2 cells. In contrast, B-1 cells have constitutive activation of ERK and NF-AT but exhibit delayed JNK and lack p38 MAPK and NF-kappaB induction upon BCR cross-linking. The lack of NF-kappaB activation in B-1 cells may be due to a lack of Akt activation in these cells. Furthermore, our study using specific inhibitors reveals that the extended survival of B-1 cells in culture is not due to the constitutive activation of ERK; nor is it due to Akt signaling or Bcl-x(L) up-regulation, since these are not induced in B-1 cells. The current findings of altered MAPK and NF-AT activation and lack of NF-kappaB induction in B-1 cells indicate that these cells have signaling properties similar to tolerant B cells that are chronically exposed to self-antigens. Indeed, BCR stimulation of B-1 cells does not lead to their full activation as indicated by their lack of maximal up-regulation of specific markers such as CD25, CD69, and CD86.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / physiology*
  • CD5 Antigens / analysis*
  • DNA-Binding Proteins / metabolism
  • Enzyme Activation
  • Hematopoietic Stem Cells / physiology*
  • Immune Tolerance*
  • Immunoglobulin M / physiology
  • Immunoglobulin Variable Region / analysis
  • Isoenzymes / metabolism
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred BALB C
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • NFATC Transcription Factors
  • Nuclear Proteins*
  • Phospholipase C gamma
  • Protein Serine-Threonine Kinases*
  • Proto-Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins c-akt
  • Receptors, Antigen, B-Cell / physiology*
  • Transcription Factors / metabolism
  • Type C Phospholipases / metabolism

Substances

  • CD5 Antigens
  • DNA-Binding Proteins
  • Immunoglobulin M
  • Immunoglobulin Variable Region
  • Isoenzymes
  • NF-kappa B
  • NFATC Transcription Factors
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • Receptors, Antigen, B-Cell
  • Transcription Factors
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • Mitogen-Activated Protein Kinases
  • Type C Phospholipases
  • Phospholipase C gamma