首页> 外文会议>Academic Committee conference of Shanghai key lab of stomatology >Apoptotic gene expression by human periodontal ligament cells following cyclic stretch
【24h】

Apoptotic gene expression by human periodontal ligament cells following cyclic stretch

机译:循环拉伸后人牙周膜细胞凋亡基因的表达

获取原文

摘要

Background and Objective: Periodontal ligament cells play an important role in maintaining homeostasis of periodontal tissue upon mechanical force loading caused by mastication or orthodontic force. Previous studies revealed force-driven periodontal ligament cell death via apoptosis, but the force-sensing genes assigned to the apoptotic pathway have not been fully characterized. The present study aimed to identify force-sensing genes implicated in the apoptotic pathway in periodontal ligament cells. Material and Methods: Human periodontal ligament cells were exposed to 20% stretch strain for 6 or 24 h, and the differential expression of 84 genes implicated in the apoptotic pathway were quantified by real-time PCR array technology. Results: Ten and 11 genes showed upregulated expression after 6 and 24 h stretches, respectively, and there were two downregulated genes in response to both 6 and 24 h stretches. These genes included those encoding the tumor necrosis factor ligand family (TNFSF8), tumor necrosis factor receptor family (FAS, TNFRSF10B, TNFRSF11B, TNFRSF25 and CD27), the Bcl-2 family (BAG3, BAK1, BCL2L11 and BCLAF1), the caspase family (CASP5 and CASP7), the inhibitor of apoptosis proteins family (BTRC3, BIRC6 and NAIP), the caspase recruitment domain family (RIPK2 and PYCARD) and the death domain family (DAPK1), as well as an oncogene (BRAF). Conclusion: This study identified several forcesensing genes implicated in the apoptotic pathway in periodontal ligament cells and should facilitate future studies on force-driven apoptosis by providing putative target genes.
机译:背景与目的:牙周膜细胞在咀嚼或正畸力引起的机械力负荷下,对维持牙周组织的稳态起着重要的作用。先前的研究表明,力驱动的牙周膜细胞通过凋亡而死亡,但是分配给细胞凋亡途径的力感应基因尚未完全表征。本研究旨在鉴定与牙周膜细胞凋亡途径有关的力敏感基因。材料与方法:将人牙周膜细胞暴露于20%拉伸应变下6或24 h,并通过实时PCR阵列技术定量检测涉及凋亡途径的84个基因的差异表达。结果:10和11个基因分别在6和24 h延伸后表达上调,而两个基因在6和24 h延伸响应中下调。这些基因包括编码肿瘤坏死因子配体家族(TNFSF8),肿瘤坏死因子受体家族(FAS,TNFRSF10B,TNFRSF11B,TNFRSF25和CD27),Bcl-2家族(BAG3,BAK1,BCL2L11和BCLAF1),胱天蛋白酶家族的基因(CASP5和CASP7),凋亡蛋白家族的抑制剂(BTRC3,BIRC6和NAIP),胱天蛋白酶募集结构域家族(RIPK2和PYCARD)和死亡结构域家族(DAPK1)以及癌基因(BRAF)。结论:本研究鉴定了与牙周膜细胞凋亡途径有关的几种增强基因,并应通过提供推定的靶基因来促进对力驱动凋亡的进一步研究。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号