Burns Kevin D
Kidney Research Centre, Division of Nephrology, The Ottawa Hospital, Ottawa Health Research Institute, University of Ottawa, Ottawa, Ontario, Canada.
Curr Opin Nephrol Hypertens. 2007 Mar;16(2):116-21. doi: 10.1097/MNH.0b013e3280123c0e.
The intrarenal renin-angiotensin system contributes to the progression of chronic kidney disease. Angiotensin-converting enzyme-2 is a recently identified protein that is highly expressed in the kidney and results in formation of angiotensin-(1-7). This manuscript highlights current information on the localization and function of angiotensin-converting enzyme-2 in the kidney, along with recent studies on the role of the enzyme in hypertension, glomerulosclerosis, and diabetic nephropathy.
Angiotensin-converting enzyme-2 is expressed in relative abundance in the proximal tubule and metabolizes angiotensin II to angiotensin-(1-7). Angiotensin-converting enzyme-2 also catalyzes conversion of angiotensin I to angiotensin-(1-9), which is cleaved to angiotensin-(1-7) by angiotensin-converting enzyme. In mice, gene deletion of angiotensin-converting enzyme-2 elevates blood pressure responses to angiotensin II, and increases renal angiotensin II levels. Male angiotensin-converting enzyme-2-deficient mice exhibit accelerated glomerulosclerosis. In early diabetic nephropathy, proximal tubular angiotensin-converting enzyme-2 expression and activity are increased, suggesting that the enzyme may counterregulate the effects of local angiotensin II.
Angiotensin-converting enzyme-2 appears to be critical in determining the balance between the intrarenal effects of angiotensin II and angiotensin-(1-7). Angiotensin-converting enzyme-2 could thereby represent a target for novel therapeutic approaches in a variety of kidney disorders.
肾内肾素 - 血管紧张素系统参与慢性肾脏病的进展。血管紧张素转换酶2是最近发现的一种在肾脏中高表达的蛋白质,可生成血管紧张素 -(1 - 7)。本文着重介绍了血管紧张素转换酶2在肾脏中的定位和功能的当前信息,以及该酶在高血压、肾小球硬化和糖尿病肾病中作用的最新研究。
血管紧张素转换酶2在近端小管中相对大量表达,并将血管紧张素II代谢为血管紧张素 -(1 - 7)。血管紧张素转换酶2还催化血管紧张素I转化为血管紧张素 -(1 - 9),后者被血管紧张素转换酶裂解为血管紧张素 -(1 - 7)。在小鼠中,血管紧张素转换酶2基因缺失会增强对血管紧张素II的血压反应,并增加肾脏血管紧张素II水平。雄性血管紧张素转换酶2缺陷小鼠表现出加速的肾小球硬化。在早期糖尿病肾病中,近端小管血管紧张素转换酶2的表达和活性增加,提示该酶可能对局部血管紧张素II的作用起反向调节作用。
血管紧张素转换酶2似乎在决定血管紧张素II和血管紧张素 -(1 - 7)的肾内效应之间的平衡中起关键作用。因此,血管紧张素转换酶2可能成为多种肾脏疾病新型治疗方法的靶点。