| Literature DB >> 15585835 |
Xiaocui Zhu1, Rebecca Hart, Mi Sook Chang, Jong-Woo Kim, Sun Young Lee, Yun Anna Cao, Dennis Mock, Eugene Ke, Brian Saunders, Angela Alexander, Joella Grossoehme, Keng-Mean Lin, Zhen Yan, Robert Hsueh, Jamie Lee, Richard H Scheuermann, David A Fruman, William Seaman, Shankar Subramaniam, Paul Sternweis, Melvin I Simon, Sangdun Choi.
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.Entities:
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Year: 2004 PMID: 15585835 DOI: 10.4049/jimmunol.173.12.7141
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422