期刊文献+

牵张应变诱导人牙周膜细胞凋亡信号通路初探

Study on stretching force-induced apoptosis mechanism of human periodontal ligament cells
下载PDF
导出
摘要 目的通过研究Caspase酶在牵张应变作用下的变化,来初步探讨其引起人牙周膜细胞(HPDLCs)凋亡的可能机制。方法体外培养HPDLCs,利用动态机械应变细胞加载装置对HPDLCs加载1%、10%和20%的动态牵张应变6、12、24、48 h,利用酶标仪检测Caspase-3活性以及添加Caspase-8和Caspase-9阻断剂后Caspase-3活性。结果 Caspase-3活性具有一定的时间和应变值依赖性,各应变组细胞的Caspase-3活性在加载24 h时达到峰值,Caspase-9阻断剂可以显著降低Caspase-3的活性,而Caspase-8却并没有明显作用同时发现。结论 Caspase-9激活Caspase-3介导的凋亡通路参与了牵张应变诱导HPDLCs的凋亡。 Objective To explore the apoptosis mechanism of human periodontal ligament cells ( HPDLCs) induced by Caspase un-der stretching force. Methods HPDLCs were cultured in vitro, and cells were stretched by dynamic mechanical strain 1%, 10% and 20% for 6 h, 12 h, 24 h and 48 h. The Caspase?3 activity was measured after stretching in PDL cells that were treated with a specific inhibitor of either Caspase?8 or Caspase?9 prior to the application of stretching force. Results The activity of Caspase?3 increased sub-stantially in a time and force dependent manner after the application of a cyclic stretching force. It reached a peak at 24 h. The Caspase?9 inhibitor abolished the stretching force-induced activation of Caspase?3, whereas the Caspase?8 inhibitor demonstrated no effect. Con-clusion Cyclic stretching force can induce apoptosis in HPDLCs through the activation of Caspase?3 via the Caspase?9 signaling cas-cade.
出处 《口腔医学》 CAS 2016年第7期599-602,共4页 Stomatology
关键词 牵张应变 凋亡 Caspase酶 人牙周膜细胞 stretching force apoptosis Caspase HPDLCs
  • 相关文献

参考文献2

二级参考文献98

  • 1胡司淦,蔡鑫.Fas系统在冠心病和慢性心力衰竭中的变化及意义[J].蚌埠医学院学报,2006,31(4):439-440. 被引量:6
  • 2刘娜,刘俊田.失巢凋亡在As斑块破裂中的作用及机制[J].中国药理学通报,2007,23(3):298-301. 被引量:9
  • 3杨绍杰,孟金萍,屈祎,刘云波.细胞凋亡信号传导通路的研究进展[J].中国比较医学杂志,2007,17(5):297-301. 被引量:72
  • 4Jackson TC, Rani A, Kumar A, Foster TC. Regional hippocampal differences in AKT survival signaling across the lifespan: implica- tions for CA1 vulnerability with aging. Cell Death Differ 2009, 16: 439-448.
  • 5Nie K, Yu JC, Fu Y, Cheng HY, Chen FY, Qu Y, et al. Age-related decrease in constructive activation of Akt/PKB in SAMP10 hip- pocampus. Biochem Biophys Res Commun 2009, 378:103-107.
  • 6Andjelkovic M, Alessi DR, Meier R, Fernandez A, Lamb NJ, Frech M, et al. Role oftranslocation in the activation and function of pro- tein kinase B. J Biol Chem 1997, 272: 31515-31524.
  • 7Bellacosa A, Chan TO, Ahmed NN, Datta K, Malstrom S, Stokoe D, et al. Akt activation by growth factors is a multiple-step process: the role of the PH domain. Oncogene 1998, 17: 313-325.
  • 8Song G, Ouyang G, Bao S. The activation of Akt/PKB signaling pathway and cell survival. J Cell Mol Med 2005, 9: 59-71.
  • 9Pastor MD, Garcia-Yebenes I, Fradejas N, P6rez-Ortiz JM, Mora- Lee S, Tranque P, et al. mTOR/S6 kinase pathway contributes to astrocyte survival during ischemia. J Biol Chem 2009, 284(33): 22067-22078.
  • 10Condorelli F, Salomoni P, Cotteret S, Cesi V, Srinivasula SM, AI- nemri ES, et al. Caspase cleavage enhances the apoptosis-inducing effects of BAD. Mol Cell Biol 2001, 21: 3025-3036.

共引文献183

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部