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Role of galectin-1 on epithelial-to-mesenchymal transition induced by high glucose peritoneal dialysate in human peritoneal mesothelial cells / 中南大学学报(医学版)
Journal of Central South University(Medical Sciences) ; (12): 190-196, 2012.
Artigo em Chinês | WPRIM | ID: wpr-814698
ABSTRACT
OBJECTIVE@#To investigate the expression of galectin-1 with the stimulation of peritoneal dialysis solution (PDS) and its role in the epithelial-to-mesenchymal transition (EMT) in human peritoneal mesothelial cells (HPMCs).@*METHODS@#HPMCs were stimulated with PDS containing different concentrations of high glucose (1.5%, 2.5%, and 4.25%). After 24 h, mRNA and protein expressions of galectin-1,vimentin, and zo-1 were analyzed with real-time PCR and Western blot, respectively. Liposome transfected siRNA technique was used to knock down the expression of galectin-1 and the effect of galectin-1 siRNA on the EMT of HPMCs was also observed under 4.25% PDS condition.@*RESULTS@#mRNA expression of galectin-1 in HPMCs increased in PDS groups, especially in group with 4.25% PDS (P<0.05). Protein expression of galectin-1 in HPMCs significantly increased in PDS groups with a dose dependent manner (P<0.05).Expression of vimentin in HPMCs significantly increased in PDS groups, especially in groups of 2.5% PDS and 4.25% PDS (P<0.05), but zo-1 expression markedly decreased (P<0.05). The expression of galectin-1 correlated positively with vimentin (P<0.05) but negatively with zo-1 (P<0.05). Expression of vimentin in groups of 4.25% PDS was markedly inhibited (P<0.05) by galectin-1 siRNA, whereas zo-1 expression was significantly increased (P<0.05).@*CONCLUSION@#Galectin-1 can mediate high glucose PDS-induced EMT in HPMCs and may be a new target for the prevention and treatment of peritoneal fibrosis.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Peritônio / Farmacologia / RNA Mensageiro / Soluções para Diálise / Células Cultivadas / Diálise Peritoneal / Biologia Celular / Galectina 1 / Células Epiteliais / Fibrose Peritoneal Limite: Humanos Idioma: Chinês Revista: Journal of Central South University(Medical Sciences) Ano de publicação: 2012 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Peritônio / Farmacologia / RNA Mensageiro / Soluções para Diálise / Células Cultivadas / Diálise Peritoneal / Biologia Celular / Galectina 1 / Células Epiteliais / Fibrose Peritoneal Limite: Humanos Idioma: Chinês Revista: Journal of Central South University(Medical Sciences) Ano de publicação: 2012 Tipo de documento: Artigo