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PMID: 3496881 Published · ppublish English Journal Article

Inhibitors of protein kinase C block activation of B lymphocytes by bacterial lipopolysaccharide.

Biochemical and biophysical research communications ·Vol. 145 ·No. 3 ·1987-06-30 ·Pages 1315-20

Rush JS, Waechter CJ

Abstract

Activation of murine splenic B lymphocytes (B cells) by bacterial lipopolysaccharide (LPS) was found to be markedly inhibited by 1-(5-isoquinolinylsulfonyl)-2-methylpiperazine (H-7) and N-[2-(methylamino)ethyl]-5-isoquinolinesulfonamide (H-8), two potent inhibitors of protein kinases. The higher sensitivity of DNA synthesis, RNA synthesis and protein N-glycosylation activity to H-7, relative to H-8, strongly supports the proposal that protein kinase C plays a critical role in the activation of B cells. A kinetic study on the time of addition of H-7 indicated that protein kinase C promoted the activation process continuously after the addition of LPS.

MeSH Terms
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine Animals B-Lymphocytes/drug effects,immunology,metabolism Cells, Cultured DNA Replication/drug effects Female Isoquinolines/pharmacology Kinetics Lipopolysaccharides/pharmacology Lymphocyte Activation/drug effects Mice Mice, Inbred DBA Piperazines/pharmacology Protein Kinase C/antagonists & inhibitors Transcription, Genetic/drug effects
Chemicals
Isoquinolines Lipopolysaccharides Piperazines 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine N-(2-(methylamino)ethyl)-5-isoquinolinesulfonamide Protein Kinase C
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Rush J S
Waechter C J
Article Info
Journal
Biochemical and biophysical research communications
Abbr.
Biochem Biophys Res Commun
ISSN
0006-291X
Published
1987-06-30
Pages
1315-20
Language
English
Region
United States
NLM ID
0372516
Subset
IM
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