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Role of PI3K/Akt signaling in hydrogen sulfide-induced alteration in expression of collagen I and III in hepatic stellate cells / 中华肝脏病杂志
Chinese Journal of Hepatology ; (12): 430-433, 2014.
Artigo em Chinês | WPRIM | ID: wpr-314023
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the role of the PI3K/Akt signaling pathway in hydrogen sulfide-induced alterations in expression of collagen I and collagen III in hepatic stellate cells.</p><p><b>METHODS</b>In vitro cultured rat hepatic stellate cells (HSC-T6) were treated with hydrogen sulfide, or left untreated for use as controls, and divided into groups for treatment with different inhibitors for the various factors involved in the PI3K/Akt signaling pathway. Reverse transcription-PCR was used to measure Collagen I and collagen III mRNA expression. Western blotting was used to detect the protein expression of PI3K and p-Akt, which are upstream proteins of the PI3K/Akt pathway.</p><p><b>RESULTS</b>Compared with the untreated control cells, the hydrogen sulfide treated cells showed elevated expression of collagen I mRNA (F =14.635, P less than 0.05), collagen III mRNA (F =14.620, P less than 0.05), PI3K protein (F =26.672, P less than 0.05), and p-Akt (F =23.522, P less than 0.05). Compared to the cells treated with hydrogen sulfide alone, the cells treated with the various inhibitors showed lower expression of collagen I mRNA (F =14.635, P less than 0.05), collagen III mRNA (F=14.620, P less than 0.05), PI3K protein (F =26.672, P less than 0.05), and p-Akt protein (F =23.522, P less than 0.05).</p><p><b>CONCLUSION</b>Hydrogen sulfide can activate the PI3K/Akt pathway and elevate the expression of collagen I and collagen III in rat hepatic stellate cells.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Farmacologia / RNA Mensageiro / Transdução de Sinais / Células Cultivadas / Fosfatidilinositol 3-Quinases / Colágeno Tipo I / Colágeno Tipo III / Proteínas Proto-Oncogênicas c-akt / Células Estreladas do Fígado / Genética Limite: Animais Idioma: Chinês Revista: Chinese Journal of Hepatology Ano de publicação: 2014 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Farmacologia / RNA Mensageiro / Transdução de Sinais / Células Cultivadas / Fosfatidilinositol 3-Quinases / Colágeno Tipo I / Colágeno Tipo III / Proteínas Proto-Oncogênicas c-akt / Células Estreladas do Fígado / Genética Limite: Animais Idioma: Chinês Revista: Chinese Journal of Hepatology Ano de publicação: 2014 Tipo de documento: Artigo