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Notch1 and Notch2 receptors regulate human and mouse gastric epithelial cell homeostasis.

机译:Notch1和Notch2受体调节人和小鼠胃上皮细胞的稳态。

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摘要

The gastric epithelium undergoes constant turnover that is maintained by a population of gastric stem cells. Gastric stem cells are under the regulation of multiple signaling pathways to promote proper epithelial homeostasis. Previous studies have shown that the Notch signaling pathway plays a crucial role in regulating epithelial differentiated cell fate, stem cell function, and epithelial cell proliferation in the stomach. My thesis work has focused on identifying the mechanisms by which Notch signaling regulates gastric epithelial cell homeostasis.;I identified Notch1 and Notch2 as the key receptors contributing to the regulation of gastric epithelial cells by Notch. Using inhibitory antibodies targeting Notch1 and Notch2, I observed a marked reduction in proliferation of both corpus and antral epithelial cells that mimicked the reduced proliferation observed with global Notch inhibition. Inhibition of Notch1 or Notch2 signaling led to an intermediate reduction in proliferation in both regions of the glandular stomach. In the antrum, inhibition of both receptors resulted in a general increase in expression of markers of differentiated cells, including enteroendocrine, surface mucous, and deep mucous cells. Inhibition of both receptors also led to increased secretory granules in antral cells and expression of secretory products from other regions of the gastrointestinal tract, including the corpus and intestine.;To investigate if Notch signaling is intrinsic to the epithelium, I refined the conditions for gastric organoid establishment from mouse and human antrum and corpus tissue. In mouse and human antral and corpus organoids, inhibition of Notch1 and Notch2 resulted in a reduction of organoid growth similar to that seen with global Notch inhibition. In corpus organoids, inhibition of either Notch1 or Notch2 resulted in an intermediate disruption of organoid growth. However, in antral organoids, inhibition of Notch1 mimicked growth similar to that seen with global inhibition, suggesting that Notch1 may play a more significant role in antral organoid growth than Notch2.;In summary, my thesis work has expanded the understanding of the role of Notch in gastric epithelial homeostasis. I have illustrated an important role for the Notch1 and Notch2 receptors in regulating gastric epithelial proliferation and differentiation in vivo and in vitro.
机译:胃上皮经历恒定的更新,这由一组胃干细胞维持。胃干细胞在多种信号传导途径的调控下,促进适当的上皮稳态。先前的研究表明,Notch信号通路在调节胃中上皮分化的细胞命运,干细胞功能和上皮细胞增殖中起着至关重要的作用。我的论文工作集中在确定Notch信号调节胃上皮细胞稳态的机制。我确定Notch1和Notch2是Notch调节胃上皮细胞的关键受体。使用针对Notch1和Notch2的抑制性抗体,我观察到了and体和肛门上皮细胞的增殖明显减少,这与用整体Notch抑制观察到的增殖减少相似。 Notch1或Notch2信号的抑制导致腺胃的两个区域中增殖的中间减少。在胃窦中,两种受体的抑制作用导致分化细胞标志物的表达普遍增加,这些标志物包括肠内分泌,表面粘液和深层粘液细胞。两种受体的抑制还导致胃窦细胞分泌颗粒的增加以及胃肠道其他区域(包括the体和肠道)分泌产物的表达。为了研究Notch信号是否是上皮细胞固有的,我改良了胃的条件从小鼠和人的胃窦和体组织建立类器官。在小鼠和人的肛门和体类器官中,Notch1和Notch2的抑制导致类器官生长的减少,类似于整体Notch抑制所见。在语料库类器官中,Notch1或Notch2的抑制导致类器官生长的中间中断。然而,在窦性类器官中,对Notch1的抑制作用类似于整体抑制作用,这表明Notch1可能比Notch2在窦性类动物生长中发挥更重要的作用。缺口在胃上皮稳态中。我已经说明了Notch1和Notch2受体在体内和体外调节胃上皮细胞增殖和分化中的重要作用。

著录项

  • 作者

    Gifford, Gail B.;

  • 作者单位

    University of Michigan.;

  • 授予单位 University of Michigan.;
  • 学科 Physiology.;Genetics.;Oncology.
  • 学位 Ph.D.
  • 年度 2016
  • 页码 204 p.
  • 总页数 204
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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