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Restricted expression of somatostatin receptor 3 to primary cilia in the pancreatic islets and adenohypophysis of mice

机译:生长抑素受体3在小鼠胰岛和垂体腺垂体中向纤毛的表达受到限制

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摘要

The primary cilium is now considered to function as a fundamental, not rudimentary, structure for mechanical and chemical sensing by individual cells. Primary cilia in neurons express type III adenylyl cyclase (ACIII) and GPCRs for somatostatin (somatostatin receptor 3, SSTR3), serotonin, and melanin-concentrating hormone. The present immunohistochemical and electron microscopic study revealed an abundant occurrence of SSTR3-expressing solitary cilia in insulin- and growth hormone-secreting cells of the mouse. The SSTR3 immunoreactivity was restricted to the plasma membrane of cilia in both cell types, differing from previously reported immunohistochemical localization of SSTRs to cell bodies. The primary cilia in the islet cells were longer than those in the pituitary cells and extended for a long distance in the intercellular canalicules endowed with microvilli. No other endocrine organs were provided with the SSTR3-expressing primary cilia, while the primary cilia in these organs were frequently immunolabeled with ACIII antibody. Since the somatostatin inhibition of both insulin and GH release is regulated mainly by SSTR1 and SSTR5, the primary cilia expressing SSTR3 may be involved in a signaling which differs from that via other SSTR subtypes expressing in cell bodies.
机译:现在,初级纤毛被认为是单个细胞进行机械和化学传感的基本结构,而不是基本结构。神经元的初级纤毛表达III型腺苷酸环化酶(ACIII)和生长抑素(生长抑素受体3,SSTR3),5-羟色胺和黑色素浓缩激素的GPCR。目前的免疫组织化学和电子显微镜研究表明,在小鼠的胰岛素和生长激素分泌细胞中大量存在表达SSTR3的孤立纤毛。在两种细胞类型中,SSTR3的免疫反应性都限于纤毛的质膜,这与先前报道的SSTR在细胞体中的免疫组织化学定位不同。胰岛细胞中的原纤毛比垂体细胞中的纤毛长,并且在具有微绒毛的细胞间小管中长距离延伸。没有向其他内分泌器官提供表达SSTR3的原发纤毛,而这些器官中的原发纤毛经常被ACIII抗体免疫标记。由于生长抑素对胰岛素和GH释放的抑制作用主要受SSTR1和SSTR5调节,因此表达纤毛的原发纤毛可能参与的信号转导不同于通过细胞体中表达的其他SSTR亚型的信号转导。

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