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[血管紧张素原基因的结构与表达调控]

[Structure and regulation of the expression of the angiotensinogen gene].

作者信息

Ibarra-Rubio M E, Pedraza-Chaverrí J

机构信息

Depto. de Nefrología y Metabolismo Mineral, Instituto Nacional de la Nutrición Salvador Zubirán, México, D.F.

出版信息

Rev Invest Clin. 1993 Jul-Aug;45(4):387-98.

PMID:8235138
Abstract

Angiotensinogen is a glycoprotein synthesized mainly in hepatocytes and secreted into the circulation. Angiotensinogen is cleaved by the enzyme renin to produce angiotensin I, which is further converted into a vasoconstricting peptide, angiotensin II, the biologically active peptide of the renin angiotensin system. The concentration of angiotensinogen is rate-limiting in the production of angiotensin I and therefore plays an important role in the regulation of angiotensin II production. The development of recombinant DNA technology has introduced new directions for the study of the angiotensinogen molecule. The human, rat and mouse angiotensinogen gene contains five exons interrupted by four intervening sequences and spans 12 kb approximately. In its 5' flanking region multiple regulating elements, as well as the major control elements, are present. The cloning and sequencing of the angiotensinogen cDNA demonstrates the similarity of angiotensinogen to various serine protease inhibitors produced by the liver and was the beginning of studies looking for new physiological roles of angiotensinogen, in addition to the substrate for renin. The circulating levels of angiotensinogen are altered in many different physiological and pathological states. High levels of this protein are seen in hypercorticism, inflammation, pregnancy, and contraceptive therapy, and low levels are associated with adrenal insufficiency and converting enzyme inhibition. These variations are mostly due to modifications of the hepatic biosynthesis under the control of hormonal factors such as glucocorticoid, estrogen, thyroid hormone, insulin and angiotensin II. In addition, it has been found that these changes in the hepatic biosynthesis are due mainly to changes in the angiotensinogen gene expression.

摘要

血管紧张素原是一种主要在肝细胞中合成并分泌入血液循环的糖蛋白。血管紧张素原被肾素酶切割产生血管紧张素I,血管紧张素I再进一步转化为一种血管收缩肽——血管紧张素II,它是肾素血管紧张素系统的生物活性肽。血管紧张素原的浓度在血管紧张素I的产生过程中起限速作用,因此在血管紧张素II产生的调节中起重要作用。重组DNA技术的发展为血管紧张素原分子的研究引入了新方向。人、大鼠和小鼠的血管紧张素原基因包含五个外显子,被四个间隔序列打断,跨度约为12kb。在其5'侧翼区域存在多个调控元件以及主要控制元件。血管紧张素原cDNA的克隆和测序表明血管紧张素原与肝脏产生的各种丝氨酸蛋白酶抑制剂相似,这也是除了作为肾素底物之外寻找血管紧张素原新生理作用研究的开端。血管紧张素原的循环水平在许多不同的生理和病理状态下会发生改变。在皮质醇增多症、炎症、妊娠和避孕治疗中可见该蛋白水平升高,而低水平与肾上腺功能不全和转化酶抑制有关。这些变化主要是由于在糖皮质激素、雌激素、甲状腺激素、胰岛素和血管紧张素II等激素因子控制下肝脏生物合成的改变。此外,已发现肝脏生物合成的这些变化主要是由于血管紧张素原基因表达的改变。

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