...
首页> 外文期刊>Experimental and therapeutic medicine >Inhibition of periderm removal in all-trans retinoic acid-induced cleft palate in mice
【24h】

Inhibition of periderm removal in all-trans retinoic acid-induced cleft palate in mice

机译:在小鼠中抑制全反式视黄酸诱导的腭裂腭裂的抑制作用

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Cleft palate is a common craniofacial birth defect. The aim of the present study was to investigate the effect of excess all-trans retinoic acid (atRA) on periderm removal and the disappearance of basal medial edge epithelial (MEE) cells during palatogenesis, particularly during the stage prior to contact. atRA (200 mg/kg) was administered to C57BL/6N mice at embryonic day (E) 12.0 by gavage. Fetal palates were processed and analyzed by histology and electron microscopy. Single palate shelf peridermal cells were removed and cultured in the presence of atRA (3 mu M) only or in the presence of or the caspase inhibitor, Z-VAD (100 mu M) only, for 48 h. Once cultured, morphological changes were analyzed by histological staining and electron microscopy. A TUNEL assay was used to detect apoptotic neurons. Paired palatal shelves with periderm removal were cultured in the presence of atRA (3 mu M) only or in the presence of Z-VAD (100 mu M) only for 48 h and analyzed by hematoxylin and eosin staining. At E14.5, medial edge epithelium periderm was retained in the atRA-treated palates but had been shed prior to contact in the control groups. In addition, atRA was revealed to disrupt the cell cycle in the periderm by downregulating p21. Furthermore, atRA inhibited apoptosis in the periderm and basal MEE cells; however, atRA exhibited no effect on basement membrane degradation in single palatal organ culture. Additionally, once paired palates were cultured for 48 h, all of the groups in which the periderm had been removed exhibited confluence of the embryonic palatal mesenchyme. The present results suggest that periderm removal is inhibited in atRA-induced cleft palate in mice and that removal of the periderm contributes to EPM confluence in vitro.
机译:腭裂是一个常见的颅面出生缺陷。本研究的目的是探讨过量的全反式视黄酸(ATRA)对甘然油期间基础内侧上皮(MEE)细胞的胰腺去除和消失的影响,特别是在接触之前的阶段。 ATRA(200mg / kg)在胚胎日(e)12.0的胚胎日(e)给予C57BL / 6N小鼠。通过组织学和电子显微镜加工和分析胎儿腭。除去单一腭架壁细胞,仅在ATRA(3μm)存在下或在胱天蛋白酶抑制剂(仅在胱天蛋白酶抑制剂(100μm)存在下培养48小时。一旦培养,通过组织学染色和电子显微镜分析了形态学变化。用于检测凋亡神经元的调节。在ATRA(3μm)存在下或仅在Z-VAD(100μm)存在下仅培养具有平坦去除的成对的腭架仅为48小时,并通过苏木精和曙红染色分析。在E14.5,内侧边缘上皮细胞萼片保留在ATRA处理的腭,但在对照组中接触之前已经脱落。此外,通过下调P21,揭示了ATRA以破坏间形的细胞周期。此外,ATRA抑制了睑板和基底细胞中的细胞凋亡;然而,ATRA在单一腭器官培养中没有对地下室膜降解的影响。另外,一旦将配对的腭裂培养48小时,所有的胚芽被除去胚状腭间表单的汇合。本结果表明,在小鼠的ATRA诱导的腭裂中抑制了胰腺去除,并且去除Periderm在体外贡献EPM汇合。

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