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Y-27632 reduces the MMP2 and MMP9 expression in endothelial cell via inhibition of ROCK signal pathway / 中南大学学报(医学版)
Article em Zh | WPRIM | ID: wpr-814997
Biblioteca responsável: WPRO
ABSTRACT
OBJECTIVE@#To explore the effect of ROCK inhibitor Y-27632 on the matrix metalloproteinase 2 and 9 (MMP2 and MMP9) gene expression and activity in tumor necrosis factor α (TNF-α)-treated human umbilical vein endothelial cell (HUVEC).
@*METHODS@#HHUVEC was divided into 3 groups, a control group, a TNF-α group, and a TNF-α plus Y-27632 group. The expressions of vascular cell adhesion molecule-1 (VCAM-1), intercellular adhesion molecule-1 (ICAM-1), MMP2 and MMP9 were examined by real-time PCR. The MMP2/9 activity was measured by gelatin zymography.
@*RESULTS@#Compared to the control group, the mRNA expressions of ICAM-1, VCAM-1, MMP2 and MMP9 were increased TNF-α-treated cells, which were suppressed by ROCK inhibitor (P<0.01). The MMP2/9 activity was elevated in TNF-α-treated cells, which was reversed by ROCK inhibitor (P<0.05).
@*CONCLUSION@#ROCK inhibitor can suppress TNF-α-induced inflammation in endothelial cells through down-regulation of MMP2/9.
Assuntos
Texto completo: 1 Índice: WPRIM Assunto principal: Piridinas / Veias Umbilicais / Transdução de Sinais / Regulação para Baixo / Células Cultivadas / Fator de Necrose Tumoral alfa / Molécula 1 de Adesão Intercelular / Molécula 1 de Adesão de Célula Vascular / Metaloproteinase 2 da Matriz / Metaloproteinase 9 da Matriz Limite: Humans Idioma: Zh Revista: Journal of Central South University(Medical Sciences) Ano de publicação: 2016 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Piridinas / Veias Umbilicais / Transdução de Sinais / Regulação para Baixo / Células Cultivadas / Fator de Necrose Tumoral alfa / Molécula 1 de Adesão Intercelular / Molécula 1 de Adesão de Célula Vascular / Metaloproteinase 2 da Matriz / Metaloproteinase 9 da Matriz Limite: Humans Idioma: Zh Revista: Journal of Central South University(Medical Sciences) Ano de publicação: 2016 Tipo de documento: Article