首页> 美国卫生研究院文献>Acta Histochemica et Cytochemica >Immunohistochemical Localization of Barx2 in the Developing Fetal Mouse Submandibular Glands
【2h】

Immunohistochemical Localization of Barx2 in the Developing Fetal Mouse Submandibular Glands

机译:Barx2在发育中的胎儿小鼠下颌下腺中的免疫组织化学定位

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

The development of mouse submandibular gland (SMG) begins at embryonic day 11.5–12 (E11.5–12), during which successive rounds of epithelial clefting and branching create complex epithelial tree-like structures. Homeobox genes regulate place-dependent morphogenesis, including epithelial-mesenchymal interactions, and control the expression patterns of signaling molecules. The Barx2 containing Homeobox exerts several key roles in development. Some studies have shown that the Barx2 plays important roles in the epithelial-mesenchymal interactions of organogenesis. However, the mechanisms of Barx2 associated with the development of SMG are obscure. In this study, we demonstrated for the first time the exact spatial and temporal Barx2 expression pattern in SMG epithelial tissue during development using immunohistochemical staining and Real-Time quantitative PCR. Barx2 was expressed in the nucleus of the epithelial cells located in the proliferative and differentiative regions of the developing SMG during the early development stages (E11.5–E13.5). After the E14.5-time period, the expression gradually decreased, and at E16.5, expression mostly disappeared despite the fact that evidence of cytodifferentiation, such as the appearance of proacinar cells, distinct lumen formation, and secretory products, was beginning to be observed. Results of Real-Time PCR demonstrated that the amount of Barx2 mRNA expression in SMG was maximal on E14.5, and gradually decreased by E18.5. These results indicate that Barx2 is associated with early stage epithelial tissue development, and can be a useful epithelial marker of the SMG during early developmental stages.
机译:小鼠下颌下腺(SMG)的发育始于胚胎的第11.5–12天(E11.5–12),其间连续的上皮裂隙和分支回合形成了复杂的上皮树状结构。同源盒基因调节位置依赖性形态发生,包括上皮-间质相互作用,并控制信号分子的表达模式。包含Homeobox的Barx2在开发中扮演着多个关键角色。一些研究表明,Barx2在器官发生的上皮-间质相互作用中起重要作用。但是,与SMG发生有关的Barx2机制尚不清楚。在这项研究中,我们首次使用免疫组织化学染色和实时定量PCR证明了SMG上皮组织在发育过程中Barx2确切的时空表达模式。在早期发育阶段(E11.5-E13.5),Barx2在位于发育中的SMG增殖和分化区域的上皮细胞核中表达。在E14.5时间段后,表达逐渐降低,在E16.5时,表达消失了很多,尽管事实是细胞分化的迹象(例如前突肌细胞的出现,明显的管腔形成和分泌产物)开始出现。被观察。实时荧光定量PCR结果表明,SMG中Barx2 mRNA的表达在E14.5上最大,而在E18.5上逐渐降低。这些结果表明Barx2与早期上皮组织发育有关,并且可以在早期发育阶段作为SMG的有用上皮标记。

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