Literature DB >> 6332133

Phorbol esters inhibit murine B cell differentiation to immunoglobulin secretion but not proliferation.

P C Isakson, L Simpson.   

Abstract

Bacterial lipopolysaccharide (LPS) induces resting B cells to proliferate and to secrete IgM. We have found that addition of phorbol esters (PE) such as phorbol myristate acetate (PMA) to murine B cells specifically inhibits LPS-induced IgM secretion but not proliferation. PMA is extremely potent, with half-maximal inhibition occurring at about 10 pM. The effect on B cells appears to be due to interaction with PE receptors, because a series of PE have similar potencies for tumor promotion, binding to receptors, and inhibition of IgM secretion. PE also inhibit IgM secretion induced by T cell-derived lymphokines and LPS-induced IgG secretion. Results of these studies suggest that the protein kinase C, with which PE interact, plays an important role in the regulation of B cell differentiation and may also provide a powerful tool for dissecting molecular events involved in induction of Ig secretion.

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Year:  1984        PMID: 6332133

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  4 in total

1.  Mitogenic response of murine B lymphocytes to Salmonella typhimurium lipopolysaccharide requires protein kinase C-dependent late tyrosine phosphorylations.

Authors:  A Mey; J P Revillard
Journal:  Infect Immun       Date:  1998-06       Impact factor: 3.441

2.  Regulation of immunoglobulin transcription rates and mRNA processing in proliferating normal B lymphocytes by activators of protein kinase C.

Authors:  E Högbom; I L Mårtensson; T Leanderson
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

3.  Antiimmunoglobulin-treated B cells respond to a B cell differentiation factor for IgG1.

Authors:  P C Isakson
Journal:  J Exp Med       Date:  1986-07-01       Impact factor: 14.307

4.  Interleukin 5 and interleukin 2 cooperate with interleukin 4 to induce IgG1 secretion from anti-Ig-treated B cells.

Authors:  J M Purkerson; M Newberg; G Wise; K R Lynch; P C Isakson
Journal:  J Exp Med       Date:  1988-09-01       Impact factor: 14.307

  4 in total

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