Literature DB >> 3155861

B cells that simultaneously express surface IgM and IgE in Nippostrongylus brasiliensis-infected SJA/9 mice do not provide evidence for isotype switching without gene deletion.

I M Katona, J F Urban, F D Finkelman.   

Abstract

Recently, it has been reported that in SJA/9 mice infected with Nippostrongylus brasiliensis there are increased numbers of lymphoid cells positive for surface IgM and IgE (sIgM+ and sIgE+) even though they fail to secrete IgE, that both the sIgM and sIgE on these cells are intrinsic, and that there has been no deletion of genes for the Ig heavy chain constant region in these cells. These observations support a nondeletional model for Ig isotype switching. We have now reexamined the nature of sIgE on sIgE+ spleen and mesenteric lymph node cells of N. brasiliensis-infected SJA/9 mice, and the following observations lead us to believe that this sIgE is cytophilic rather than intrinsic: (i) Only approximately 50% of the N. brasiliensis-infected SJA/9 mice have detectable percentages of sIgE+ lymphoid cells. All mice with detectable sIgE+ lymphocytes have lymphocytes positive for intracytoplasmic IgE (cIgE+) and secrete IgE in vitro, while cIgE+ cells and IgE secretion are absent from N. brasiliensis-infected SJA/9 mice that lack sIgE+ cells. (ii) SJA/9 B lymphocytes have receptors for IgE: expression of these receptors is increased in N. brasiliensis-infected mice that have sIgE+ lymphocytes, but not in infected SJA/9 mice that lack sIgE+ lymphocytes. (iii) Treatment of sIgM+ sIgD+ sIgE+ cells for 1 min with dilute acid removes most sIgE but does not affect expression of sIgM or sIgD. (iv) The removal of mouse IgE from sIgE+ B cells facilitates the binding of exogenous rat IgE. (v) The small amount of sIgE that is reexpressed during a period of in vitro culture after acid treatment is blocked by inclusion of exogenous rat IgE in the culture medium. These observations show that most sIgM+ sIgE+ B cells in N. brasiliensis-infected SJA/9 mice do not express intrinsic sIgE; thus studies using these cells to determine mechanisms of Ig isotype switching are inconclusive.

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Year:  1985        PMID: 3155861      PMCID: PMC397069          DOI: 10.1073/pnas.82.2.511

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  23 in total

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Journal:  J Immunol       Date:  1983-01       Impact factor: 5.422

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Journal:  Nature       Date:  1982-06-24       Impact factor: 49.962

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Journal:  Nature       Date:  1980-06-12       Impact factor: 49.962

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Journal:  Nature       Date:  1982-03-25       Impact factor: 49.962

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Journal:  Ann N Y Acad Sci       Date:  1982       Impact factor: 5.691

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Journal:  J Immunol       Date:  1980-07       Impact factor: 5.422

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Journal:  J Immunol       Date:  1980-02       Impact factor: 5.422

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  12 in total

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Authors:  Oezcan Talay; Donghong Yan; Hans D Brightbill; Elizabeth E M Straney; Meijuan Zhou; Ena Ladi; Wyne P Lee; Jackson G Egen; Cary D Austin; Min Xu; Lawren C Wu
Journal:  Nat Immunol       Date:  2012-02-26       Impact factor: 25.606

2.  Coexpression of mu and gamma 1 heavy chains can occur by a discontinuous transcription mechanism from the same unrearranged chromosome.

Authors:  M Nolan-Willard; M T Berton; P Tucker
Journal:  Proc Natl Acad Sci U S A       Date:  1992-02-15       Impact factor: 11.205

Review 3.  The molecular basis of immunoglobulin class switching: switch transcription versus switch recombination.

Authors:  A Radbruch
Journal:  Immunol Res       Date:  1991       Impact factor: 2.829

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Authors:  C F Webb; M D Cooper; P D Burrows; J A Griffin
Journal:  Proc Natl Acad Sci U S A       Date:  1985-08       Impact factor: 11.205

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6.  Switch recombination in normal IgA1+ B lymphocytes.

Authors:  J Irsch; S Irlenbusch; J Radl; P D Burrows; M D Cooper; A H Radbruch
Journal:  Proc Natl Acad Sci U S A       Date:  1994-02-15       Impact factor: 11.205

7.  Unique maturation program of the IgE response in vivo.

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Journal:  Immunity       Date:  2007-02-08       Impact factor: 31.745

8.  TRAF2 Deficiency in B Cells Impairs CD40-Induced Isotype Switching That Can Be Rescued by Restoring NF-κB1 Activation.

Authors:  Rachel A Woolaver; Xiaoguang Wang; Yonatan Dollin; Ping Xie; Jing H Wang; Zhangguo Chen
Journal:  J Immunol       Date:  2018-10-19       Impact factor: 5.422

9.  Imbalanced PTEN and PI3K Signaling Impairs Class Switch Recombination.

Authors:  Zhangguo Chen; Andrew Getahun; Xiaomi Chen; Yonatan Dollin; John C Cambier; Jing H Wang
Journal:  J Immunol       Date:  2015-10-23       Impact factor: 5.422

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Authors:  A Shimizu; M C Nussenzweig; H Han; M Sanchez; T Honjo
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