炎症中的ACE和ACE2:两种酶的故事。

Ravinder Reddy Gaddam, Stephen Chambers, Madhav Bhatia
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引用次数: 133

摘要

肾素-血管紧张素系统(RAS)被认为是一个协调的激素级联系统,在控制许多器官的多种功能中起着重要作用,并且比以前认为的要复杂得多。RAS继续扩大,确定了新的组成部分、功能和子系统。血管紧张素转换酶(ACE)及其新型同源物血管紧张素转换酶2 (ACE2)是参与RAS生物活性成分合成的两个关键酶。RAS的主要活性肽包括血管紧张素II (Ang II)、Ang III、Ang IV和血管紧张素-(1-7)[Ang-(1-7)],其中Ang II和Ang-(1-7)在健康和疾病中更为重要。ACE2形成的轴代表了RAS内部的内源性反调控通路,其作用与ACE轴相反。传统上认为RAS在心血管系统、代谢、细胞生长和体内平衡中起重要作用。近年来,ACE和ACE2及其肽在心脏肥大、肺动脉高压、肾小球肾炎、肺损伤、败血症和急性胰腺炎等炎症过程中发挥着关键作用。研究正在进行中,以更好地了解RAS在炎症中的作用。全面了解炎症中的RAS成分可以为治疗炎症性疾病提供新的可能性。在这篇综述中,我们根据最近的研究结果,讨论了我们目前对ACE和ACE2在炎症中的作用的理解。
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ACE and ACE2 in inflammation: a tale of two enzymes.

The renin-angiotensin system (RAS) conceived as a coordinated hormonal cascade plays an important role in controlling multiple functions in many organs and is much more complex than previously thought. The RAS has continued to expand, with the identification of new components, functions and subsystems. Angiotensin-converting enzyme (ACE) and its novel homolog angiotensin converting enzyme 2 (ACE2) are two key enzymes involved in the synthesis of bioactive components of the RAS. The main active peptides of the RAS include angiotensin II (Ang II), Ang III, Ang IV, and angiotensin-(1-7) [Ang-(1-7)] among which Ang II and Ang-(1-7) are much more important in health and disease. The axis formed by ACE2 represents an endogenous counter-regulatory pathway within the RAS, and its actions are opposite to those of the ACE axis. Conventionally the RAS has been considered to be important in the cardiovascular system, metabolism, cell growth and homeostasis. In recent years, a key role of ACE and ACE2 and their peptides has been recognized in the inflammatory process in conditions such as cardiac hypertrophy, pulmonary hypertension, glomerulonephritis, lung injury, sepsis, and acute pancreatitis. Investigations are ongoing to better understand the role of the RAS in inflammation. A comprehensive understanding of the RAS components in inflammation can provide new possibilities for therapeutic approaches against inflammatory diseases. In this review, we discuss our current understanding of the subject, based on recent findings, on the role of ACE and ACE2 in inflammation.

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