To characterize gene expression in activated mast cells more comprehensively than heretofore, we surveyed the changes in genetic transcripts by the method of serial analysis of gene expression in the RBL-2H3 line of rat mast cells before and after they were stimulated through their receptors with high affinity for immunoglobulin E (FcεRI). A total of 40,759 transcripts derived from 11,300 genes were analyzed. Among the diverse genes that had not been previously associated with mast cells and that were constitutively expressed were those for the cytokine macrophage migration inhibitory factor neurohormone receptors such as growth hormone- releasing factor and melatonin and components of the exocytotic machinery. In addition, several dozen transcripts were differentially expressed in response to antigen-induced clustering of the FcεRI. Included among these were the genes for preprorelaxin, mitogen-activated protein kinase kinase 3, and the dual specificity protein phosphatase, rVH6. Significantly, the majority of genes differentially expressed in this well-studied model of mast cell activation have not been identified before this analysis.
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2 November 1998
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November 02 1998
Characterization of Gene Expression in Resting and Activated Mast Cells
Huaxian Chen,
Huaxian Chen
From the *Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases and the ‡National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20892
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Michael Centola,
Michael Centola
From the *Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases and the ‡National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20892
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Stephen F. Altschul,
Stephen F. Altschul
From the *Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases and the ‡National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20892
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Henry Metzger
Henry Metzger
From the *Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases and the ‡National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20892
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Huaxian Chen
From the *Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases and the ‡National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20892
Michael Centola
From the *Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases and the ‡National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20892
Stephen F. Altschul
From the *Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases and the ‡National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20892
Henry Metzger
From the *Arthritis and Rheumatism Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases and the ‡National Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, Maryland 20892
Address correspondence to Huaxian Chen, Arthritis and Rheumatism Branch, 10 Center Drive MSC 1820, Bethesda, MD 20892-1820. Phone: 301-496-1565; Fax: 301-402-0012; E-mail: [email protected]
Received:
July 28 1998
Revision Received:
August 27 1998
Online ISSN: 1540-9538
Print ISSN: 0022-1007
1998
J Exp Med (1998) 188 (9): 1657–1668.
Article history
Received:
July 28 1998
Revision Received:
August 27 1998
Citation
Huaxian Chen, Michael Centola, Stephen F. Altschul, Henry Metzger; Characterization of Gene Expression in Resting and Activated Mast Cells . J Exp Med 2 November 1998; 188 (9): 1657–1668. doi: https://doi.org/10.1084/jem.188.9.1657
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