Effects of lipid rafts on signal transmembrane transduction mediated by c-Met / 中华肝脏病杂志
Zhonghua ganzangbing zazhi
; Zhonghua ganzangbing zazhi;(12): 449-452, 2008.
Article
de Zh
| WPRIM
| ID: wpr-332207
Bibliothèque responsable:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To study the effects of lipid rafts on cell signal transmembrane transduction mediated by c-Met.</p><p><b>METHODS</b>After HepG2Cells were treated with MbCD to disrupt the lipid rafts and were treated with artificial recombination hepatocyte growth factor to activate c-Met, the activities of PLCr1/PKC, PI3K/Akt and MAPK signaling pathways in HepG2 cells were analyzed using Western blot.</p><p><b>RESULTS</b>(1) After disruption of lipid rafts with MbCD, phosphorylation of PLCr1 decreased by 35% (P = 0.022); the content of PLCr in the cytoplasm increased by 1.75 fold (P = 0.017); PLCr1 conjugated with membrane decreased by 30% (P = 0.037). (2) The content of PKB in the cytosol decreased by 38% (P = 0.028), and the phosphorylation level of PKB conjugated with membrane decreased by 14% (P = 0.041). At the same time, PDK translocation from cytosol to the plasma membrane and its activation were inhibited by treatment with MbCD. (3) Treatment with MbCD had no significant effect on ErK/MAPK, p38/MAPK and JNK/MAPK signaling pathways.</p><p><b>CONCLUSION</b>Disruption of lipid rafts with MbCD inhibits the activation of PLCr1/PKC and PI3K/PKB signaling pathways by HGF/cMet, but has no effect on MAPK signaling pathway.</p>
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Phosphorylation
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Transduction du signal
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Phosphatidylinositol 3-kinases
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Protéines proto-oncogènes c-met
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Mitogen-Activated Protein Kinases
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Microdomaines membranaires
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Phospholipase C gamma
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Protéines proto-oncogènes c-akt
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Cellules HepG2
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Métabolisme
Limites du sujet:
Humans
langue:
Zh
Texte intégral:
Zhonghua ganzangbing zazhi
Année:
2008
Type:
Article