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Regulation of Ganoderma lucidum Polysaccharides on Cytotoxic T Lymphocytes Induced by Dendritic Cells in vitro

机译:灵芝多糖对树突状细胞体外诱导的细胞毒性T淋巴细胞的调节

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This research studied the regulatory effects of Ganoderma lucidum polysaccharides (GL-PS) on cytotoxicity and mechanism of specific cytotoxic T lymphocytes (CTL) induced by dendritic cells (DC) in vitro during the stage of antigen presentation. Cultured murine bone marrow-derived DC were pulsed with P815 tumor cell lysates and co-incubated with or without various concentrations of GL-PS (0.8, 3.2, or 12.8mg·L<'-1>) at the same time. P815 specific CTL were induced by spleen lymphocytes stimulated with mature DC. Non-adherent cells and culture supernatants were harvested on d 5 for analysis of specific cytotoxicity with lactate dehydrogenase (LDH) activity assay, mRNA expression of IFN-γ, granzyme B with RT-PCR assay, and protein expression of IFN-γ, granzyme B with ELISA or western blot assay, respectively. Three concentrations of GL-PS could promote LDH activities released into culture supernatants (P <0.01). It also increased mRNA expression of IFN-γ in CTL (GL-PS 12.8mg·L<'-1> vs RPMI medium 1640, P<0.05) and granzyme B in CTL (P<0.01). Protein production of IFN-γ in culture supernatants (P<0.05) and protein expression of granzyme B in CTL (GL-PS 12.8mg·L<'-1> vs RPMI medium 1640, P<0.05) were also augmented by GL-PS. GL-PS was shown to promote the cytotoxicity of specific CTL induced by DC which pulsed with P815 tumor antigen during the stage of antigen presentation, and the mechanisms of cytotoxicity was believed to be going through IFN-γ and granzyme B pathways.
机译:本研究研究了灵芝多糖(GL-PS)在抗原呈递阶段体外对树突状细胞(DC)诱导的特异性细胞毒性T淋巴细胞(CTL)的细胞毒性和机制的调控作用。用P815肿瘤细胞裂解物对培养的鼠源于骨髓的DC进行脉冲处理,并同时在有或没有各种浓度的GL-PS(0.8、3.2或12.8mg·L'-1)的条件下共同孵育。通过成熟DC刺激的脾淋巴细胞诱导P815特异性CTL。在第5天收集非贴壁细胞和培养上清液,用乳酸脱氢酶(LDH)活性测定法分析特异性细胞毒性,用RT-PCR测定IFN-γ,粒酶B的mRNA表达,以及IFN-γ,粒酶的蛋白表达。 B分别用ELISA或western blot测定。三种浓度的GL-PS均可促进释放到培养上清液中的LDH活性(P <0.01)。它还增加了CTL中的IFN-γ的mRNA表达(GL-PS 12.8mg·L'-1 vs RPMI培养基1640,P <0.05)和颗粒酶B在CTL中的表达(P <0.01)。 GL-还增强了培养上清液中IFN-γ的蛋白产量(P <0.05)和CTL中颗粒酶B的蛋白表达(GL-PS 12.8mg·L <-1)与RPMI培养基1640,P <0.05)。 PS。研究表明,GL-PS可以促进DC诱导的特异性CTL的细胞毒性,该DC在抗原呈递阶段以P815肿瘤抗原脉冲产生,并且据认为细胞毒性的机制是通过IFN-γ和颗粒酶B途径进行的。

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