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Construction of shRNA expression vectors for autophagy gene beclin 1 and their downregulation effect on caspase-9 / 生物医学工程学杂志
J. biomed. eng ; Sheng wu yi xue gong cheng xue za zhi;(6): 413-419, 2007.
Article em Zh | WPRIM | ID: wpr-357686
Biblioteca responsável: WPRO
ABSTRACT
The shRNA expression vectors were constructed and transfected via lipofectamine into HeLa cells. Real time-ploymerase chain reaction (RT-PCR) and Western blot were used for detecting the expression of mRNA and protein of Beclin1 in transfected cells. Flow cytometry was employed to observe the effect of transfection on the apoptosis and cell cycle of HeLa, and proliferation was analyzed by MTT assay. The expression of caspase-9 in transfection cells was also detected by RT-PCR and Western blot. The constructed vectors significantly inhibited the expressin of mRNA and the protein of Beclin1 in HeLa cells. The growth of transfected cells was promoted, and less apoptosis cells were identified in these cells. After transfection of the constructed vectors into HeLa cells, the expression of caspase-9 was effectively inhibited. All of these indicate that autophagy and apoptosis are two types of programmed cell death, that autophagy gene Beclin 1 plays an important role in these two types, and that defect of autophagy and apoptosis may be important in tumor genesis.
Assuntos
Texto completo: 1 Índice: WPRIM Assunto principal: Autofagia / RNA Mensageiro / Células HeLa / Transfecção / Regulação para Baixo / Apoptose / RNA Interferente Pequeno / Interferência de RNA / Proteínas Reguladoras de Apoptose / Caspase 9 Tipo de estudo: Prognostic_studies Limite: Humans Idioma: Zh Revista: J. biomed. eng / Sheng wu yi xue gong cheng xue za zhi Ano de publicação: 2007 Tipo de documento: Article
Texto completo: 1 Índice: WPRIM Assunto principal: Autofagia / RNA Mensageiro / Células HeLa / Transfecção / Regulação para Baixo / Apoptose / RNA Interferente Pequeno / Interferência de RNA / Proteínas Reguladoras de Apoptose / Caspase 9 Tipo de estudo: Prognostic_studies Limite: Humans Idioma: Zh Revista: J. biomed. eng / Sheng wu yi xue gong cheng xue za zhi Ano de publicação: 2007 Tipo de documento: Article