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首页> 外文期刊>Journal of cell biology >Retrovirus-mediated expression of preprosomatostatin: posttranslational processing, intracellular storage, and secretion in GH3 pituitary cells.
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Retrovirus-mediated expression of preprosomatostatin: posttranslational processing, intracellular storage, and secretion in GH3 pituitary cells.

机译:逆转录病毒介导的前前列腺抑素表达:翻译后加工,细胞内储存和GH3垂体细胞分泌。

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摘要

Somatostatin (SRIF) is a 14-amino acid peptide hormone that is synthesized as part of a larger precursor, preproSRIF, consisting of a signal peptide and a proregion of 80-90 amino acids. The mature hormone, which is located at the carboxyl terminus of the precursor, is preceded by a single pair of basic amino acids. We are studying preproSRIF to investigate intracellular sorting, proteolytic processing, and storage of peptide hormone precursors in the secretory pathway. We used a retroviral expression vector to achieve the high levels of precursor synthesis which are necessary for detailed characterization of processing intermediates and mature somatostatin. Recombinant retroviruses containing RNA transcripts encoding anglerfish preproSRIF I were used to infect rat pituitary GH3 cells which secrete growth hormone and prolactin, neither of which are substrates for endoproteolytic cleavage. In these cells preproSRIF was accurately processed to the mature hormone with an efficiency of approximately 75%. Of the newly synthesized mature SRIF, 55% was sorted into the regulated secretory pathway and released in response to the secretagogue 8-Br-cAMP. The remaining 45% of mature SRIF and residual unprocessed precursor was rapidly secreted. In contrast to SRIF, only 5% of newly synthesized endogenous growth hormone was stored intracellularly, whereas 95% was sorted to the constitutive pathway and secreted rapidly with kinetics identical to proSRIF. Our results show that proSRIF processing is not necessarily dependent on a specific protease found only in SRIF-producing cells and suggest that proteolytic cleavage is not restricted to cells that process endogenous hormones. Moreover, these results demonstrate that GH3 cells have the capacity to discriminate between endogenous and foreign hormones and target the foreign molecule significantly more efficiently to the regulated secretory pathway.
机译:生长抑素(SRIF)是一种14个氨基酸的肽激素,作为较大的前体preproSRIF的一部分合成,由信号肽和80-90个氨基酸的前区组成。位于前体羧基末端的成熟激素之前是一对碱性氨基酸。我们正在研究preproSRIF,以研究细胞内分选,蛋白水解过程和分泌途径中肽激素前体的存储。我们使用逆转录病毒表达载体来实现高水平的前体合成,这对于加工中间体和成熟生长抑素的详细表征是必需的。含有编码angle鱼preproSRIF I的RNA转录本的重组逆转录病毒被用于感染大鼠垂体GH3细胞,后者分泌生长激素和催乳激素,两者都不是内切蛋白水解的底物。在这些细胞中,preproSRIF被精确加工成成熟激素,效率约为75%。在新合成的成熟SRIF中,有55%被归类为受调节的分泌途径并响应促分泌素8-Br-cAMP而释放。剩余的45%成熟的SRIF和残留的未加工前体被迅速分泌。与SRIF相比,新合成的内源性生长激素中只有5%储存在细胞内,而95%被分类到组成型途径并以与proSRIF相同的动力学迅速分泌。我们的结果表明proSRIF加工不一定依赖于仅在产生SRIF的细胞中发现的特定蛋白酶,并且表明蛋白水解切割不限于加工内源激素的细胞。而且,这些结果表明GH3细胞具有区分内源激素和外源激素并将外源分子显着更有效地靶向调节的分泌途径的能力。

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