Kumar Rajesh, Boim Mirian A
Division of Molecular Cardiology, Department of Medicine, Texas A&M Health Science Center, College of Medicine, Temple, Texas, USA.
Curr Opin Nephrol Hypertens. 2009 Jan;18(1):33-9. doi: 10.1097/MNH.0b013e32831a9e20.
The renin-angiotensin system (RAS) has undergone continuous advancement since the initial identification of renin as a pressor agent. Traditionally considered a circulatory system, the RAS is now known to exist as a tissue system as well. Recently, the tissue RAS has been further categorized as intracellular and extracellular. Owing to the unique location, the intracellular RAS encompasses new components, such as cathepsin D and chymase, which participate in intracellular angiotensin (Ang) II synthesis. In this review, evidence of the intracellular RAS and the mechanism of Ang II synthesis in various cell types will be discussed.
A physiological role for intracellular Ang II in vascular and cardiac cells has recently been demonstrated. Evidence of intracellular Ang II generation has been shown in several cell types, particularly cardiac, renal, and vascular. Importantly, intracellular synthesis of Ang II is more prominent in hyperglycemic conditions and generally involves angiotensin-converting enzyme-dependent and angiotensin-converting enzyme-independent mechanisms.
There is significant diversity in the mechanism of intracellular synthesis of Ang II in various cell types and pathological conditions. These observations suggest that a therapeutic intervention to block the RAS should take into consideration the nature of the disorder and the cell type involved.
自肾素最初被鉴定为一种升压因子以来,肾素-血管紧张素系统(RAS)不断发展。传统上认为RAS是一个循环系统,现在已知它也以组织系统的形式存在。最近,组织RAS进一步分为细胞内和细胞外RAS。由于其独特的位置,细胞内RAS包含新的成分,如组织蛋白酶D和糜酶,它们参与细胞内血管紧张素(Ang)II的合成。在本综述中,将讨论细胞内RAS的证据以及各种细胞类型中Ang II合成的机制。
最近已证明细胞内Ang II在血管和心脏细胞中具有生理作用。在几种细胞类型中已显示出细胞内Ang II生成的证据,特别是在心脏、肾脏和血管中。重要的是,在高血糖条件下,Ang II的细胞内合成更为显著,并且通常涉及血管紧张素转换酶依赖性和血管紧张素转换酶非依赖性机制。
在各种细胞类型和病理条件下,Ang II细胞内合成机制存在显著差异。这些观察结果表明,阻断RAS的治疗干预应考虑疾病的性质和所涉及的细胞类型。