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PMID: 6229582 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

B cell activation. IV. Induction of cell membrane depolarization and hyper-I-A expression by phorbol diesters suggests a role for protein kinase C in murine B lymphocyte activation.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 132 ·No. 3 ·1984-03-00 ·Pages 1472-8

Monroe JG, Niedel JE, Cambier JC

Abstract

Analysis of the effects of phorbol diesters on mouse B lymphocyte kinase C activity, membrane potential, mI-A expression, and cell cycle state are reported. Results indicate that the phorbol diesters PMA and 4 beta-PDD, which are potent tumor promoters, activate partially purified B cell protein kinase C and stimulate B cell membrane depolarization and increased mI-A expression. The analog 4 alpha-PDD has none of these effects. Similarly, none of the phorbol diesters tested promoted G0 to G1 transition of B lymphocytes. Results are consistent with the possibility that the transmembrane signal transduction mediated by cell membrane immunoglobulin, which results in membrane depolarization and increased I-A antigen expression, operates via activation of protein kinase C.

MeSH Terms
Animals B-Lymphocytes/cytology,enzymology,immunology Cell Cycle/drug effects Enzyme Activation/drug effects Histocompatibility Antigens Class II/analysis Lymphocyte Activation/drug effects Membrane Potentials/drug effects Mice Mice, Inbred BALB C Phorbol Esters/pharmacology Phorbols/pharmacology Protein Kinase C Protein Kinases/metabolism Tetradecanoylphorbol Acetate/pharmacology
Chemicals
Histocompatibility Antigens Class II Phorbol Esters Phorbols phorbol-12,13-didecanoate Protein Kinases Protein Kinase C Tetradecanoylphorbol Acetate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Monroe J G
Niedel J E
Cambier J C
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1984-03-00
Pages
1472-8
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NIAID NIH HHS · AI 16128 · United States
NIAID NIH HHS · AI 18308 · United States
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