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Journal of Southern Medical University ; (12): 1190-1193, 2006.
Artigo em Chinês | WPRIM | ID: wpr-334960

RESUMO

<p><b>OBJECTIVE</b>To observe the effects of temporary acid exposure on cell proliferation and extracellular signal-regulated protein kinase (ERK) activity in normal human esophageal epithelial cells in vitro.</p><p><b>METHODS</b>Normal human esophageal epithelial cells cultured in vitro were exposed to acidic media (pH 4.0-6.5) for 3 to 60 min, and the control cells were cultured at pH 7.3. MTT assay and flow cytometry were employed for cell proliferation assessment. The expression of phosphorylated ERK1/2 protein was determined by immunoblotting.</p><p><b>RESULTS</b>Esophageal epithelial cells with acid exposure for 3 min exhibited a significant increase in cell proliferation, increased number of cells in S phase and enhanced expression of phosphorylated ERK1/2 protein. Acid exposure of the esophageal epithelial cells exceeding 6 min resulted in depressed proliferation and decreased S-phase cells, and cell proliferation induced by acid exposure was abolished by pretreatment with U0126.</p><p><b>CONCLUSION</b>Temporary acid stimulus increases cell proliferation of normal human esophageal epithelial cells in vitro by activating the ERK pathway.</p>


Assuntos
Humanos , Ácidos , Farmacologia , Western Blotting , Butadienos , Farmacologia , Proliferação de Células , Células Cultivadas , Meios de Cultura , Farmacologia , Inibidores Enzimáticos , Farmacologia , Células Epiteliais , Biologia Celular , Metabolismo , Esôfago , Biologia Celular , MAP Quinases Reguladas por Sinal Extracelular , Metabolismo , Concentração de Íons de Hidrogênio , Imuno-Histoquímica , Queratina-14 , Nitrilas , Farmacologia , Transdução de Sinais , Fatores de Tempo
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