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Cyclins/CDKs在Fas介导细胞凋亡过程中的变化及其机制 被引量:3

Changes of Cyclins/CDKs in Fas-mediated apoptosis and the mechansim
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摘要 目的 探讨Cyclins/CDKs在Fas介导的细胞凋亡过程中的作用机制.方法 以白血病细胞株(Molt-4和Jurkat细胞株)和健康人的外周血淋巴细胞为载体,用人重组Fas配体诱导稳定而又典型的细胞周期特异性凋亡模型 用Cyclin/DNA双参数流式细胞术检测Cyclins的表达 用Western blot法检测CDK1和CDK2的磷酸化位点以及进一步确认Cyclins的表达.结果 研究rhFasL诱导Jurkat、Molt-4细胞和进入细胞周期的PBL凋亡时,G1期的Cyclin D3在发生凋亡效应前明显升高、发生凋亡效应后明显下降,而Cyclin E则先明显下降后升高,Cyclin A和B1无明显变化 CDK2 Thr-160位点的磷酸化水平在发生凋亡效应前后均明显下降,CDK1 Thr-161、Tyr-15位点的磷酸化水平在发生凋亡效应后稍有下降 G0期淋巴细胞则不能被诱导出明显的细胞凋亡.结论 Fas介导的细胞凋亡的发生与细胞是否通过限制点进入细胞周期有关,细胞凋亡发生于晚G1期时G1期Cyclin E的表达下降以至不能磷酸化或者磷酸化CDK2不全,在检测点的监督下DNA受损的细胞不能通过G1/S交界进入S期而发生细胞凋亡.在凋亡发生后期Cyclins/CDK的变化与细胞被阻滞在G1期有关. Objective To study the changes of Cyclins/CDKs expression in Fas-mediated apoptosis, and the action mechanism in leukaemia cell lines and peripheral blood lymphocytes (PBL) in vitro.Methods The target cells--leukaemia cell lines and activated PBL stimulated by phytohemagglutinin were incubated with recombinant human Fas ligand for 6 to 36 h, and the changes of Cyclins expression that related to the duration of inducing apoptosis was detected by Cyclin/DNA bi-parameter flow cytometry. Rb protein and the phosphorylation site of CDK1 and CDK2 were checked by Western blotting. Results Cyclin D3 expression was increased and Cyclin E expression decreased evidently, and the expression of Cyclins A and B1 had no significant change before the induction of Fas-mediated apoptosis in Jurkat, Molt-4 cell lines and PBL which entering cell cycle progression, till the late stage of inducing apoptosis in these cells the expression of Cyclin D3 was decreased, while Cyclin E increased. Meanwhile, apoptosis couldn' t be induced by rhFas ligand in G0-phase PBL. The level of CDK2 Thr-160 phosphorylation was decreased through the induction of Fas-mediated apoptosis evidently. The phosphorylation of CDK1 had no significant changes. Conclusion Fas-mediated apoptosis was located at late G1-phase and determined by whether the target cells had passed through the restriction point to cell division cycle or not. And the cell cycle specificity of Fas-mediated apoptosis was the result of the cells with DNA damage being blocked at late G1-phase,due to the decrease of Cyclin E expression and hypophosphorylation of CDK2 and under the surveillance of G1-phase check point. The changes of Cyclins expression at the late stage of Fas-mediated apoptosis is the result of cell arrest at G1-stage.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2010年第11期1660-1662,共3页 Chinese Journal of Experimental Surgery
关键词 脱噬作用 流式细胞术 Apoptosis Flow cytometry
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  • 1张波,陈剑英,陈道达,王国斌.Cyelin E影响DNA损伤药物对乳腺癌细胞的治疗敏感性[J].中华实验外科杂志,2007,24(1):9-11. 被引量:5
  • 2Vedinden L,Vanden Bempt I,Eelen G,et al. The E2F regulated gene Chkl is highly expressed in triple-negative estrogen receptor/proges- terone receptor/HER-2 breast carcinomas [ J ]. Cancer Res, 2007,67 (14) :6574-6581.
  • 3Lundgren K, Holm K, Nordenskjold B, et al. Gene products of chromo- some 1 l q and their association with CCND1 gene amplification and tamoxifen resistance in premenopausal breast cancer[ J]. Breast Canc- er Res,2008,10(5) :81.
  • 4Lain MH, Liu Q, Elledge SJ, et al. Chkl is haploinansufficient for mul- tiple functions critical to tumor suppression [ J ]. Cancer Cell, 2004,6 ( 1 ) :45-59.
  • 5Yaffe MB, Reinhardt HC. Kinases that control the cell cycle in re- sponse to DNA damage: Chkl, Chk2, and MK2. [ J ]. Curt Opin Cell Bio1,2009,21 ( 2 ) :245-255.
  • 6Zaehos G,Rainey MD,Gillespie DA. Chkl-dependent S-M checkpoint delay in vertebrate cells is linked to maintenance of viable replieation structure [ J ]. Mol Cell Biol, 2005,25 ( 2 ) : 563-574.
  • 7Ng CP, Lee HC, Ho CW, et al. Differential mode of regulation of the checkpoint kinases CHKI and CHK2 by their regulatory domains[J]. J Biol Chem,2004,279 (10) : 8808-8819.
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