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Subcellular characteristics of functional intracellular renin-angiotensin systems

机译:功能性细胞内肾素-血管紧张素系统的亚细胞特征

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The renin-angiotensin system (RAS) is now regarded as an integral component in not only the development of hypertension, but also in physiologic and pathophysiologic mechanisms in multiple tissues and chronic disease states. While many of the endocrine (circulating), paracrine (cell-to-different cell) and autacrine (cell-to-same cell) effects of the RAS are believed to be mediated through the canonical extracellular RAS, a complete, independent and differentially regulated intracellular RAS (iRAS) has also been proposed. Angiotensinogen, the enzymes renin and angiotensin-converting enzyme (ACE) and the angiotensin peptides can all be synthesized and retained intracellularly. Angiotensin receptors (types I and 2) are also abundant intracellularly mainly at the nuclear and mitochondrial levels. The aim of this review is to focus on the most recent information concerning the subcellular localization, distribution and functions of the iRAS and to discuss the potential consequences of activation of the subcellular RAS on different organ systems.
机译:如今,肾素-血管紧张素系统(RAS)不仅是高血压的发展,而且在多种组织和慢性疾病状态下的生理和病理生理机制中也被视为不可或缺的组成部分。虽然RAS的许多内分泌(循环),旁分泌(细胞至不同细胞)和自分泌(细胞至相同细胞)作用被认为是通过规范的细胞外RAS介导的,但它是完整,独立且差异调节的还提出了细胞内RAS(iRAS)。血管紧张素原,肾素和血管紧张素转化酶(ACE)以及血管紧张素肽都可以合成并保留在细胞内。血管紧张素受体(I型和2型)在细胞内也很丰富,主要在核和线粒体水平上。这篇综述的目的是集中于有关iRAS的亚细胞定位,分布和功能的最新信息,并讨论亚细胞RAS活化在不同器官系统上的潜在后果。

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