| Literature DB >> 8670418 |
G Tokiwa1, I Dikic, S Lev, J Schlessinger.
Abstract
The c-Jun amino-terminal kinase (JNK) is activated by various heterotrimeric guanine nucleotide-binding protein (G protein)-coupled receptors, inflammatory cytokines, and stress signals. Yet, upstream mediators that link extracellular signals with the JNK signaling pathway are currently unknown. The tyrosine kinase Pyk2 was activated by tumor necrosis factor alpha, by ultraviolet irradiation, and by changes in osmolarity. Overexpression of Pyk2 led to activation of JNK, and a dominant-negative mutant of Pyk2 interfered with ultraviolet light- or osmotic shock-induced activation of JNK. Pyk2 represents a cell type-specific, stress-sensitive mediator of the JNK signaling pathway.Entities:
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Year: 1996 PMID: 8670418 DOI: 10.1126/science.273.5276.792
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728