Journal article
Growth inhibition of a B cell clone mediated by ligation of IL-4 receptors or membrane IgM
The Journal of immunology (1950), Vol.150(7), pp.2565-2574
04/01/1993
DOI: 10.4049/jimmunol.150.7.2565
PMID: 8454843
Abstract
The development of B cell tolerance is believed to involve negative signaling to the B cell derived from the binding of Ag to the B cell surface Ig (sIg). B cell clones that receive negative signals via sIg may provide useful models for studying the mechanisms of negative signaling. We have recently identified a previously undescribed mouse B cell clone, CHB3, which receives growth-inhibitory signals through the binding of IL-4 to its IL-4R or through ligation of its sIgM, but not its sIgD, molecules. Data presented here demonstrate that the negative signal delivered by sIgM, but not that delivered by IL-4R, requires protein kinase C activation and elevated intracellular Ca2+, and is associated with the tyrosine phosphorylation of a number of proteins. Thus, the IL-4R signaling pathway appears to be divergent from the sIgM-mediated pathway. However, growth inhibition mediated via both sIgM and IL-4R can be partially counteracted by a signal delivered through the MHC class II molecule.
Details
- Title: Subtitle
- Growth inhibition of a B cell clone mediated by ligation of IL-4 receptors or membrane IgM
- Creators
- Gail A Bishop - Department of Microbiology, University of Iowa, Iowa City 52242Luis M RamirezGary A Koretzky
- Resource Type
- Journal article
- Publication Details
- The Journal of immunology (1950), Vol.150(7), pp.2565-2574
- DOI
- 10.4049/jimmunol.150.7.2565
- PMID
- 8454843
- NLM abbreviation
- J Immunol
- ISSN
- 0022-1767
- eISSN
- 1550-6606
- Publisher
- United States
- Grant note
- AI28847 / NIAID NIH HHS
- Language
- English
- Date published
- 04/01/1993
- Academic Unit
- Microbiology and Immunology; President
- Record Identifier
- 9984002380302771
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