Analysis of the Major Patterns of B Cell Gene Expression Changes in Response to Short-Term Stimulation with 33 Single Ligands

Xiaocui Zhu(California Institute of Technology), Rebecca Hart(California Institute of Technology), Mi Sook Chang(California Institute of Technology), Jongwoo Kim(California Institute of Technology), Sun Young Lee(California Institute of Technology), Yun Anna Cao(California Institute of Technology), Dennis Mock(San Diego Supercomputer Center), Eugene Ke(San Diego Supercomputer Center), Brian Saunders(San Diego Supercomputer Center), Angela Alexander(Toxicologie, Pharmacologie et Signalisation Cellulaire), Joella Grossoehme(Toxicologie, Pharmacologie et Signalisation Cellulaire), Keng-Mean Lin(Toxicologie, Pharmacologie et Signalisation Cellulaire), Zhen Yan(Toxicologie, Pharmacologie et Signalisation Cellulaire), Robert C. Hsueh(Toxicologie, Pharmacologie et Signalisation Cellulaire), Jamie Lee(The University of Texas Southwestern Medical Center), Richard H. Scheuermann(Toxicologie, Pharmacologie et Signalisation Cellulaire), David A Fruman(University of California, Irvine), William E. Seaman(University of California, San Francisco), Shankar Subramaniam(San Diego Supercomputer Center), Paul C. Sternweis(Toxicologie, Pharmacologie et Signalisation Cellulaire), Melvin I. Simon(California Institute of Technology), Sangdun Choi(California Institute of Technology)
The Journal of Immunology
December 1, 2004
Cited by 59

Abstract

We examined the major patterns of changes in gene expression in mouse splenic B cells in response to stimulation with 33 single ligands for 0.5, 1, 2, and 4 h. We found that ligands known to directly induce or costimulate proliferation, namely, anti-IgM (anti-Ig), anti-CD40 (CD40L), LPS, and, to a lesser extent, IL-4 and CpG-oligodeoxynucleotide (CpG), induced significant expression changes in a large number of genes. The remaining 28 single ligands produced changes in relatively few genes, even though they elicited measurable elevations in intracellular Ca(2+) and cAMP concentration and/or protein phosphorylation, including cytokines, chemokines, and other ligands that interact with G protein-coupled receptors. A detailed comparison of gene expression responses to anti-Ig, CD40L, LPS, IL-4, and CpG indicates that while many genes had similar temporal patterns of change in expression in response to these ligands, subsets of genes showed unique expression patterns in response to IL-4, anti-Ig, and CD40L.


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