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Sequential and Asynchronous Strengthening of the Influence of Temperature on the Endo- and Exocytosis of Insulin in the Isolated Vertebrata Hepatocytes: Summing up Previous Studies

机译:序贯和异步强化温度对近椎间肝细胞胰岛素的肠尿量的影响:总结以前的研究

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Insulin internalization and processing of the Insulin Receptor Complex (IRC) inside the cell are important components of the intracellular Mechanism of Insulin Action (MIA). They define the continuation of intracellular signaling of IRC and allow utilization of the parts of the complex after ligand dissociation. Traditionally, changes in the insulin regulatory system associated with the vertebrate phylogenesis have been evaluated by changes of its two elements: the hormone and its receptor. A hormone-competent cell was considered as an evolutionarily completed element of insulin regulatory system. However, previous studies of the isolated hepatocytes of four classes of vertebrates (lamprey, frog, chicken, and rat) revealed significant differences in the state of internalization of I-125-insulin and intracellular IRC processing. Radical differences were noted in the regulation of I-125-insulin internalization and the intracellular fate of the IRC. Here, cytosolic efficient insulin degradation and a complete lack of I-125-insulin exocytosis were observed in the cyclostome cells, whereas in amphibians the hormone underwent lysosomal degradation and showed low levels of exocytosis, while birds and mammals were characterized by high volumes of the excreted I-125-insulin containing proteolytic I-125-insulin fragments. Despite the established recognition of the importance of the temperature factor, a complete understanding of the molecular mechanisms underlying the temperature effects on MIA is still missing. This poorly studied problem of the MIA temperature dependence can be behind the differences in the effect of temperature on the intracellular action of insulin and IGF-I. In fact, at different phylogenetic stages, successive changes were reported for the temperature dependence of the I-125-insulin internalization and exocytosis. The following regularities were reported for the effect of temperature on the I-125-insulin internalization in isolated hepatocytes of different origin: complete lack of receptibility of the process to temperature in lampreys, receptibility of the process in a narrow range of low temperatures (0-5 degrees C) in amphibians, and flexible regulation of I-125-insulin internalization in a wide temperature range (6- 37 degrees C) in the cells from endothermic organisms. Reported data make it possible to observe three stages in the alteration of temperature regulation of I-125-insulin internalization (in cells of cyclostomes, amphibians, and endothermic organisms) and two stages of temperature regulation of I-125-insulin exocytosis in cells of amphibians, birds, and mammals. The data presented in this study reflect the specificity of the developmental reorganization of the intracellular MIA regulation and hormone utilization, and emphasize the central role of temperature in selective MIA formation during vertebrate phylogenesis.
机译:胰岛素的内化和电池内部的胰岛素受体复合物(IRC)的处理是胰岛素作用(MIA)的胞内机制的重要组成部分。他们定义IRC的细胞内信号的延续,并允许复杂的零件利用配体解离后。激素及其受体:传统上,在与脊椎动物系统发育相关的胰岛素监管制度的变化已经通过它的两个要件的变化进行评估。激素感受态细胞被认为是胰岛素调节系统的一个进化上完成元件。然而,四班脊椎动物(七鳃鳗,蛙,鸡和大鼠)的分离肝细胞的早期研究揭示了I-125-胰岛素和细胞内的IRC处理的内在状态显著差异。激进的差异在I-125-内胰岛素的调节和IRC的细胞内命运指出。在这里,胞浆高效胰岛素的降解和缺乏完整的I-125-胰岛素胞吐在cyclostome细胞中观察到,而在两栖类激素经历溶酶体降解并表现出胞外分泌水平低,而鸟类和哺乳动物被高容量的特点排泄I-125胰岛素具有蛋白水解I-125胰岛素片段。尽管温度因素的重要性的认识成立,根本上MIA温度作用的分子机制有全面的了解,至今下落不明。该研究的不良MIA温度依赖性的问题可能落后于温度对胰岛素和IGF-I的细胞内作用效果的差异。事实上,在不同的系统发育阶段,据报用于I-125胰岛素的内化和胞吐作用的温度依赖性的连续变化。以下规律报告了温度对I-125胰岛素的内化在不同来源的分离的肝细胞中的效果:完全缺乏的方法的承受力,以在七鳃鳗温度,在一个狭窄的范围内的低温度下的处理的承受力(0在两栖动物-5℃),并且在从吸热生物体细胞宽的温度范围(6- 37℃)I-125胰岛素内化的灵活调节。报告的数据使得能够在I-125胰岛素内的温度调节的改变中的细胞,观察三个阶段(在圆口,两栖动物和吸热生物体的细胞)和I-125胰岛素胞吐作用的温度调节的两个阶段两栖类,鸟类和哺乳动物。在本研究中提出的数据反映细胞内的MIA调节和激素利用的发育重组的特异性,和脊椎动物系统发育过程中强调在选择性MIA形成温度的中心作用。

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