Induction of switch recombination to the gamma 1 and epsilon immunoglobulin (Ig) heavy chain loci was examined in B cells preactivated with anti-Ig (B lymphoblasts). In B lymphoblasts cultured with interleukin 4 (IL-4), IL-5 induced the accumulation of S micro-S gamma 1 rearrangements, but not epsilon recombination. Thus, IL-5 facilitates switch recombination directed to the gamma 1 heavy chain locus by IL-4, but additional signals are required to drive rearrangements to epsilon. Lipopolysaccharide (LPS), in the presence of IL-4, induced the accumulation of both S micro-S gamma 1 and S micro-S epsilon rearrangements, and cells treated with LPS exhibited 40-50-fold more S micro-S gamma 1 rearrangements than cells cultured with IL-5. Induction of switch recombination was not always associated with secretion of the respective Ig isotype, since concentrations of IL-4 that were sufficient to direct switch recombination to gamma 1 and epsilon in blasts treated with LPS failed to elicit secretion of IgG1 and IgE. These results demonstrate differential requirements for switch recombination to the gamma 1 and epsilon loci, as well as independent regulation of Ig gene rearrangement and secretion of each isotype.
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1 June 1994
Article|
June 01 1994
Independent regulation of DNA recombination and immunoglobulin (Ig) secretion during isotype switching to IgG1 and IgE.
J M Purkerson,
J M Purkerson
Searle Research and Development, Monsanto Company, St. Louis, Missouri 63198.
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P C Isakson
P C Isakson
Searle Research and Development, Monsanto Company, St. Louis, Missouri 63198.
Search for other works by this author on:
J M Purkerson
Searle Research and Development, Monsanto Company, St. Louis, Missouri 63198.
P C Isakson
Searle Research and Development, Monsanto Company, St. Louis, Missouri 63198.
Online ISSN: 1540-9538
Print ISSN: 0022-1007
J Exp Med (1994) 179 (6): 1877–1883.
Citation
J M Purkerson, P C Isakson; Independent regulation of DNA recombination and immunoglobulin (Ig) secretion during isotype switching to IgG1 and IgE.. J Exp Med 1 June 1994; 179 (6): 1877–1883. doi: https://doi.org/10.1084/jem.179.6.1877
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