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PMID: 2466693 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Pertussis toxin activates protein kinase C and a tyrosine protein kinase in the human T cell line Jurkat.

FEBS letters ·Vol. 244 ·No. 1 ·1989-02-13 ·Pages 181-4

Thom RE, Casnellie JE

Abstract

Pertussis toxin activates T lymphocytes by a mechanism that is independent of its ADP-ribosylation activity. The toxin stimulates increases in diacylglycerol and intracellular calcium apparently by interacting with a cell surface receptor. Consistent with the production of these second messengers we have found that pertussis toxin activates protein kinase C in the Jurkat cell line. The toxin was also found to activate a tyrosine protein kinase in these cells in a manner similar to that observed with phytohemagglutinin. These results provide evidence that the mechanism of activation of T cells by pertussis toxin involves stimulating the activity of protein kinase C and a tyrosine protein kinase.

MeSH Terms
Calcium/metabolism Cell Line Diglycerides/metabolism Enzyme Activation Humans Immunoblotting Molecular Weight Pertussis Toxin Phosphorylation Phosphotyrosine Phytohemagglutinins/pharmacology Protein Kinase C/metabolism Protein-Tyrosine Kinases/metabolism T-Lymphocytes/enzymology Tetradecanoylphorbol Acetate/pharmacology Tyrosine/analogs & derivatives,metabolism Virulence Factors, Bordetella/pharmacology
Chemicals
Diglycerides Phytohemagglutinins Virulence Factors, Bordetella Phosphotyrosine Tyrosine Pertussis Toxin Protein-Tyrosine Kinases Protein Kinase C Tetradecanoylphorbol Acetate Calcium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Thom R E
Department of Pharmacology, University of Rochester, School of Medicine and Dentistry, NY 14642.
Casnellie J E
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1989-02-13
Pages
181-4
Language
English
Region
England
NLM ID
0155157
Subset
IM
Grants
NCI NIH HHS · CA 38821 · United States
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