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Tyrosine kinases are required for interferon-gamma-stimulated proliferation of Trypanosoma brucei brucei.

作者信息

Mustafa E, Bakhiet M, Jaster R, Bittorf T, Mix E, Olsson T

机构信息

Division of Neurology, Huddinge University Hospital, Stockholm, Sweden.

出版信息

J Infect Dis. 1997 Mar;175(3):669-73. doi: 10.1093/infdis/175.3.669.

DOI:10.1093/infdis/175.3.669
PMID:9041340
Abstract

The tyrosine kinase activity of Trypanosoma brucei brucei upon stimulation with interferon-gamma (IFN-gamma) was investigated. IFN-gamma induced a rapid and strong increase of tyrosine phosphorylation of several cellular proteins that reached maximum after 5 min and was followed by a decrease to control levels after 120 min. The tyrosine kinase-specific inhibitor tyrphostin A47 at a concentration of 10(-6) M reduced IFN-gamma-induced protein phosphorylation. In vitro application of 10(-6) M tyrphostin A47 to the trypanosome cultures caused a significant reduction of [3H]thymidine uptake by IFN-gamma-stimulated trypanosomes. In animals, 2 x 0.5 mg of tyrphostin A47 (injected intraperitoneally) caused a significant reduction of parasite growth compared with the vehicle dimethyl sulfoxide or the inactive compound tyrphostin A1. In conclusion, tyrosine kinases are strongly up-regulated in IFN-gamma-stimulated T. b. brucei, and specific tyrosine kinase inhibitors can prevent trypanosome growth in vitro and in vivo.

摘要

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