The Rac2 guanosine triphosphatase regulates B lymphocyte antigen receptor responses and chemotaxis and is required for establishment of B-1a and marginal zone B lymphocytes

Ben A. Croker, David M. Tarlinton, Leonie A. Cluse, Alana J. Tuxen, Amanda Light, Feng Chun Yang, David A. Williams, Andrew W. Roberts

Research output: Contribution to journalArticle

91 Scopus citations

Abstract

We have defined roles for the hemopoietic-specific Rho guanosine triphosphatase, Rac2, in B lymphocyte development and function through examination of rac2-/- mice. Rac2-deficient mice displayed peripheral blood B lymphocytosis and marked reductions in peritoneal cavity B-1a lymphocytes, marginal zone B lymphocytes, and IgM-secreting plasma cells as well as reduced concentrations of serum IgM and IgA. The rac2-/- B lymphocytes exhibited reduced calcium flux following coligation of B cell AgR and CD19 and reduced chemotaxis in chemokine gradients. T cell-independent responses to DNP-dextran were of reduced magnitude, but normal kinetics, in rac2-/- mice, while T-dependent responses to nitrophenyl-keyhole limpet hemocyanin were subtly abnormal. Rac2 is therefore an essential element in regulating B lymphocyte functions and maintaining B lymphocyte populations in vivo.

Original languageEnglish (US)
Pages (from-to)3376-3386
Number of pages11
JournalJournal of Immunology
Volume168
Issue number7
DOIs
StatePublished - Apr 1 2002
Externally publishedYes

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ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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