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首页> 外文期刊>Cell and Tissue Research >Notch signaling-mediated cell-to-cell interaction is dependent on E-cadherin adhesion in adult rat anterior pituitary
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Notch signaling-mediated cell-to-cell interaction is dependent on E-cadherin adhesion in adult rat anterior pituitary

机译:Notch信号介导的细胞 - 细胞相互作用取决于成年大鼠前脑前脑前垂体中的E-钙粘蛋白粘附

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摘要

The rat anterior pituitary is composed of hormone-producing cells, non-hormone-producing cells (referred to as folliculostellate cells) and marginal layer cells. In the adult rat, progenitor cells of hormone-producing cells have recently been reported to be maintained within this non-hormone-producing cell population. In tissue, non-hormone-producing cells construct homophilic cell aggregates by the differential expression of the cell adhesion molecule E-cadherin. We have previously shown that Notch signaling, a known regulator of progenitor cells in a number of organs, is activated in the cell aggregates. We now investigate the relationship between Notch signaling and E-cadherin-mediated cell adhesion in the pituitary gland. Immunohistochemically, Notch signaling receptor Notch2 and the ligand Jagged1 were localized within E-cadherin-positive cells in the marginal cell layer and in the main part of the anterior lobe, whereas Notch1 was localized in E-cadherin-positive and -negative cells. Activation of Notch signaling within E-cadherin-positive cells was confirmed by immunostaining of the Notch target HES1. Notch2 and Jagged1 were always co-localized within the same cells suggesting that homologous cells have reciprocal effects in activating Notch signaling. When the E-cadherin function was inhibited by exposure to a monoclonal antibody (DECMA-1) in primary monolayer cell culture, the percentage of HES1-positive cells among Notch2-positive cells was less than half that of the control. The present results suggest that E-cadherin-mediated cell attachment is necessary for the activation of Notch signaling in the anterior pituitary gland but not for the expression of the Notch2 molecule.
机译:大鼠前脑前垂体由产生激素产生的细胞,非激素产生细胞(称为毛囊细胞)和边缘层细胞。在成年大鼠中,最近据报道了产生激素产生细胞的祖细胞在这种非激素产生的细胞群体内维持。在组织中,产生非激素的细胞通过细胞粘附分子E-钙粘蛋白的差异表达来构建同性恋细胞聚集体。我们之前已经表明,在细胞聚集体中激活了凹口信号传导,在许多器官中的祖细胞的已知调节剂。我们现在研究垂体腺体中缺口信号传导和E-Cadherin介导的细胞粘附之间的关系。免疫组织化学,Notch信号传导术Notch2和配体jagged1在边缘细胞层中的E-Cadherin阳性细胞和前叶的主要部分中定位,而Notch1局部化在E-钙粘蛋白阳性和阴茎中。通过免疫染色目标HES1的免疫染色证实了E-CDHERIN阳性细胞内的凹口信号传导的激活。 Notch2和Jagged1总是在同一细胞内共定,表明同源细胞在激活凹口信号传导中具有相互作用。当通过暴露于原发性单层细胞培养物中的单克隆抗体(DECMA-1)抑制E-CADHERIN功能时,NOTCH2阳性细胞中HES1阳性细胞的百分比小于对照的一半。本结果表明,E-Cadherin介导的细胞附着是在垂体脑前腺中的凹口信号传导但不用于Notch2分子的表达所必需的。

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