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Titolo:
Down-regulation of the c-Jun N-terminal kinase (JNK) phosphatase M3/6 and activation of JNK by hydrogen peroxide and pyrrolidine dithiocarbamate
Autore:
Chen, YR; Shrivastava, A; Tan, TH;
Indirizzi:
Baylor Coll Med, Dept Immunol, Houston, TX 77030 USA Baylor Coll Med Houston TX USA 77030 Dept Immunol, Houston, TX 77030 USA
Titolo Testata:
ONCOGENE
fascicolo: 3, volume: 20, anno: 2001,
pagine: 367 - 374
SICI:
0950-9232(20010118)20:3<367:DOTCNK>2.0.ZU;2-N
Fonte:
ISI
Lingua:
ENG
Soggetto:
TUMOR-NECROSIS-FACTOR; KAPPA-B ACTIVATION; PROTEIN-KINASES; SIGNAL-TRANSDUCTION; INTRACELLULAR LEVEL; GAMMA-RADIATION; CELL-DEATH; METAL-IONS; APOPTOSIS; PATHWAY;
Keywords:
JNK; phosphatase; oxidation; metal ions;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Citazioni:
42
Recensione:
Indirizzi per estratti:
Indirizzo: Tan, TH Baylor Coll Med, Dept Immunol, M929,1 Baylor Plaza, Houston, TX 77030 USA Baylor Coll Med M929,1 Baylor Plaza Houston TX USA 77030 77030 USA
Citazione:
Y.R. Chen et al., "Down-regulation of the c-Jun N-terminal kinase (JNK) phosphatase M3/6 and activation of JNK by hydrogen peroxide and pyrrolidine dithiocarbamate", ONCOGENE, 20(3), 2001, pp. 367-374

Abstract

Oxidative stress activates the c-Jun N-terminal kinase (JNK) pathway. However, the exact mechanisms by which reactive oxygen species (ROS) activate JNK are unclear. We found that the ability of hydrogen peroxide (H2O2) to induce JNK activation varied in different cell types. Pyrrolidine dithiocarbamate (PDTC), a presumed antioxidant, induced JNK activation on its own and enhanced JNK activation by H2O2 in many cell types, including Jurkat, HEK293, and LNCaP and Tsu-Prl prostate cancer cells. The activation of JNK by PDTC, in the presence or absence of exogenous H2O2, was dependent on its chelating ability to metal ions, most likely copper ions, Despite the strong JNK-activating ability, H2O2 plus PDTC did not induce significant activation of the upstream kinases, SEK1/MKK4 and MKK7. However, the JNK inactivation rate was slower in cells treated with H2O2 pins PDTC compared with the ratein cells treated with ultraviolet C CUV-C), Treatment of H2O2 pins PDTC significantly decreased the expression levels of a JNK phosphatase, M3/6 (also named hVH-5), but not the levels of other phosphatases (PP2A and PP4), Incontrast, UV-C irradiation did not cause the down-regulation of M3/6, These results suggest that JNK activation by H2O2 plus PDTC resulted from the down-regulation of JNK phosphatases. Our data also reveal a necessity to carefully evaluate the pharmacological and biochemical properties of PDTC.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 04/07/20 alle ore 14:53:42