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Titolo:
Activation of the Jak-Stat- and MAPK-pathways by oncostatin M is not sufficient to cause growth inhibition of human glioma cells
Autore:
Halfter, H; Postert, C; Friedrich, M; Ringelstein, EB; Stogbauer, F;
Indirizzi:
Univ Munster, Neurol Clin, D-48129 Munster, Germany Univ Munster MunsterGermany D-48129 urol Clin, D-48129 Munster, Germany
Titolo Testata:
MOLECULAR BRAIN RESEARCH
fascicolo: 2, volume: 80, anno: 2000,
pagine: 198 - 206
SICI:
0169-328X(20000915)80:2<198:AOTJAM>2.0.ZU;2-H
Fonte:
ISI
Lingua:
ENG
Soggetto:
SIGNALING PATHWAY; CYCLE ARREST; M OSM; DIFFERENTIATION; INTERLEUKIN-6; RECEPTORS; LINES; ASTROCYTES; CYTOKINES; PHENOTYPE;
Keywords:
glioma; cytokines; oncostatin M; signal transduction; jak-stat; growth inhibition;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Citazioni:
26
Recensione:
Indirizzi per estratti:
Indirizzo: Halfter, H Univ Munster, Neurol Clin, Albert Schweitzer Str 33, D-48129 Munster, Germany Univ Munster Albert Schweitzer Str 33 Munster Germany D-48129
Citazione:
H. Halfter et al., "Activation of the Jak-Stat- and MAPK-pathways by oncostatin M is not sufficient to cause growth inhibition of human glioma cells", MOL BRAIN R, 80(2), 2000, pp. 198-206

Abstract

We have recently described that oncostatin M (OSM), a member of the IL-6 family of cytokines, induces the differentiation of human glioma cells in culture. Ln order to extend this studies, we analyzed the effect of OSM on other human glioma cell lines including A172, U343-MG and T98G. All of these cell Lines express the receptor components of OSM and leukemia inhibitory factor (LIF) gp130, LIFR and the OSM specific OSMR beta. Therefore, we expected these cell lines to respond to OSM and LIF. Using specific antibodies recognizing proteins of the janus kinase (Jak-)/signal transducers and activator of transcription (Stat-) signaling cascade that has been shown to transduce the signals of the IL-6 cytokines to the nucleus, we could show that Jak1, Jak2 and Tyk2, as well as the Star proteins Stat1, Stat3 and Stat5b were phosphorylated in all three cell lines by OSM and, at least in part, byLIF. Activation of the Stat proteins was also detected by EMSA which revealed complex formation on the Stat3 DNA-binding element and on a Stat5 binding site. Consistent with our recent findings, OSM treatment also induced the activation of the MAPK erk2 and the tyrosine phosphatase SHP-2 in cells of the A172, T98G and U343-MG cell lines. Although this activation pattern was very close to what we had observed in the GOS3 glioma cells, only T98G showed a growth inhibition in response to OSM while the A172 and the U343-MGcell lines did not respond to OSM treatment in terms of growth inhibition. (C) 2000 Elsevier Science B.V. All rights reserved.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 28/01/21 alle ore 10:04:35