Ia-mediated signal transduction leads to proliferation of primed B lymphocytes

J Exp Med. 1989 Sep 1;170(3):877-86. doi: 10.1084/jem.170.3.877.

Abstract

One of the most controversial questions in immunology is the molecular basis by which Th lymphocytes deliver activating signals to quiescent B lymphocytes during T cell-dependent immune responses. Recent studies suggest that T cell-dependent activation of quiescent B lymphocytes may involve signaling mediated by direct T helper cell-B cell contact. Since B cell membrane-associated MHC-encoded class II molecules (Ia) must be recognized by Th lymphocytes for generation of T cell-dependent humoral immune responses, they are obvious candidates for receptors of this signal. Here we report that stimulation of quiescent murine B cells with IL-4 and antibodies against the B cell antigen receptor for 12-16 h primes cells to proliferate in response to immobilized mIa binding ligands. In the presence of additional lymphokines, these B cells differentiate to secrete Ig of IgM and IgG classes. These results suggest that Ia molecules are receptors for direct, T helper cell-B cell contact mediated signaling that results in B cell proliferation.

Publication types

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

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology
  • B-Lymphocytes / immunology*
  • Cell Cycle
  • Histocompatibility Antigens Class II / immunology
  • Histocompatibility Antigens Class II / physiology*
  • Immunoglobulin M / immunology
  • Interleukin-4
  • Interleukins / pharmacology
  • Lymphocyte Activation*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA
  • Signal Transduction*

Substances

  • Antibodies, Monoclonal
  • Histocompatibility Antigens Class II
  • Immunoglobulin M
  • Interleukins
  • Interleukin-4