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Study on expression of cytokines mRNA induced by B7-1-transfected Raji and Jurkat cells / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 322-326, 2002.
Artigo em Chinês | WPRIM | ID: wpr-337629
ABSTRACT
To investigate the function of B7 co-stimulator in activation and differentiation of T cell, B7 gene was transfected into Raji and Jurkat cells by liposome, B7 expression in tumor cells was detected with flow cytometry, and expression of IL-2, IL-4 and IFN-gammamRNA was detected by RT-PCR. Kinetics of secretion of three cytokines was also analyzed at 4, 12, 20 and 48 hours after gene transfection. The results showed that B7(+) Raji cells could induce mRNA expression of IL-2, IL-4 and IFN-gamma on T cell surface; B7(+) Jurkat cells could induce secretion of IL-2 and IFN-gamma. However, B7(-) Raji and B7(-) Jurkat cells could not induce secretion of cytokines. Kinetics of the three cytokines secretion were different, IL-2 and IL-4 were only detectable after 4 hours of T cell activation, whereas IFN-c was detectable after 12 hours of stimulation. The peak levels of IL-2, IL-4 and IFN-gamma were found at 20 hours after activation. It was concluded that tumor cell lines transfected with B7 gene could enhance their immunocompetence, activating T cell efficiently and B7-1 play more critical role in T cell activation and differentiation.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fisiologia / RNA Mensageiro / Transfecção / Citocinas / Interleucina-4 / Interferon gama / Interleucina-2 / Antígeno B7-1 / Células Jurkat / Genética Limite: Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2002 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Fisiologia / RNA Mensageiro / Transfecção / Citocinas / Interleucina-4 / Interferon gama / Interleucina-2 / Antígeno B7-1 / Células Jurkat / Genética Limite: Humanos Idioma: Chinês Revista: Journal of Experimental Hematology Ano de publicação: 2002 Tipo de documento: Artigo