首页> 外文期刊>International immunopharmacology >Saikosaponin a inhibits the proliferation and activation of T cells through cell cycle arrest and induction of apoptosis.
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Saikosaponin a inhibits the proliferation and activation of T cells through cell cycle arrest and induction of apoptosis.

机译:皂甙a通过细胞周期停滞和凋亡诱导抑制T细胞的增殖和活化。

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摘要

In the present study, we aimed at examining the immunosuppressive activity of saikosaponin a, a triterpene saponin derived from Bupleurum falcatum L. (Umbelliferae), and the underlying mechanisms. Saikosaponin a significantly inhibited the proliferation and activation of T cells activated by concanavalin A (Con A) in a concentration-dependent manner. Additionally, it potently suppressed Con A-stimulated IL-2, IFN-gamma and TNF-alpha production in mouse T cells. Saikosaponin a also caused G0/G1 arrest of activated T cells through down-regulating the protein levels of CDK6 and Cyclin D3 and up-regulating the protein level of p27(kip). Furthermore, the compound dose-dependently induced apoptosis of Con A-activated T cells rather than those non-activated, as determined by Annexin V/PI staining. Besides, it induced a remarkable collapse of mitochondrial membrane potential and caused significant release of cytochrome c from mitochondria to cytosol. In summary, these results suggest that the G0/G1 arrest as well as the induction of apoptosis via mitochondrial pathway are involved in the immunosuppressive activity of saikosaponin a against activated T cells. This may herald a novel approach for further studies of saikosaponin a as a candidate for the treatment of inflammatory and autoimmune diseases.
机译:在本研究中,我们旨在检查柴胡皂苷a(一种来自柴胡(伞形科)的三萜皂苷)的免疫抑制活性及其潜在机制。皂苷皂苷a以浓度依赖性方式显着抑制被伴刀豆球蛋白A(Con A)激活的T细胞的增殖和活化。此外,它有效抑制Con A刺激的小鼠T细胞中IL-2,IFN-γ和TNF-α的产生。 Saikosaponin a还通过下调CDK6和Cyclin D3的蛋白水平并上调p27(kip)的蛋白水平而导致活化T细胞的G0 / G1阻滞。此外,如膜联蛋白V / PI染色所确定的,该化合物剂量依赖性地诱导了Con A激活的T细胞的凋亡,而不是未激活的那些。此外,它引起线粒体膜电位的显着崩溃,并导致细胞色素c从线粒体大量释放到细胞质中。总之,这些结果表明,G0 / G1的阻滞以及通过线粒体途径诱导的细胞凋亡均参与了皂甙A对活化T细胞的免疫抑制活性。这可能预示着一种新的方法,可以进一步研究皂苷a作为治疗炎症和自身免疫性疾病的候选药物。

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