首页> 美国卫生研究院文献>Journal of Dental Research >Excess NF-κB Induces Ectopic Odontogenesis in Embryonic IncisorEpithelium
【2h】

Excess NF-κB Induces Ectopic Odontogenesis in Embryonic IncisorEpithelium

机译:过量的NF-κB诱导胚胎切牙异位成牙上皮

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Nuclear factor kappa B (NF-κB) signaling plays critical roles in many physiological and pathological processes, including regulating organogenesis. Down-regulation of NF-κB signaling during development results in hypohidrotic ectodermal dysplasia. The roles of NF-κB signaling in tooth development, however, are not fully understood. We examined mice overexpressing IKKβ, an essential component of the NF-κB pathway, under keratin 5 promoter (K5-Ikkβ). K5-Ikkβ mice showed supernumerary incisors whose formation was accompanied by up-regulation of canonical Wnt signaling. Apoptosis that is normally observed in wild-type incisor epithelium was reduced in K5-Ikkβ mice. The supernumerary incisors in K5-Ikkβ mice were found to phenocopy extra incisors in mice with mutations of Wnt inhibitor, Wise. Excess NF-κB activity thus induces an ectopic odontogenesis program that is usually suppressed under physiological conditions.
机译:核因子κB(NF-κB)信号传导在许多生理和病理过程中起着关键作用,包括调节器官发生。发育过程中NF-κB信号的下调导致多汗症外胚层发育不良。但是,尚未完全了解NF-κB信号在牙齿发育中的作用。我们检查了在角蛋白5启动子(K5-Ikkβ)下过表达IKKβ(NF-κB通路的重要组成部分)的小鼠。 K5-Ikkβ小鼠显示出多余的门牙,其形成伴随经典Wnt信号的上调。在K5-Ikkβ小鼠中,通常在野生型门牙上皮中观察到的凋亡减少。发现K5-Ikkβ小鼠的多余门牙表型复制了Wnt抑制剂Wise突变的小鼠的额外门牙。因此,过量的NF-κB活性会诱发异位牙生成程序,该程序通常在生理条件下被抑制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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