Department of Biological Chemistry, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
Trends Cardiovasc Med. 1994 May-Jun;4(3):110-6. doi: 10.1016/1050-1738(94)90062-0.
The renin-angiotensin system in mammals represents a complex cascade of tightly regulated proteolytic enzymes and peptide products. One important product, angiotensin II (Ang-II), is a circulating hormone that displays a wide range of physiologic effects in many tissues, including those of the cardiovascular system. It is well known that Ang-II increases the contractile state of vascular smooth muscle and cardiac myocytes by triggering multiple intracellular responses following its binding to specific receptor sites. Some of the signal transduction mechanisms that underlie these responses are understood, while others are not defined at present. Further, there has been much recent interest in Ang-II-evoked signaling, since the renin-angiotensin system has been associated with the development of cardiovascular disease. Thus, the identification of Ang-II-stimulated signal transduction mechanisms will illuminate the underlying principles of normal hormone-regulated cardiovascular homeostasis as well as those involved in pathologic processes such as human hypertension, cardiac arrhythmias, and the cellular remodeling that follows vascular injury or sustained pressure overload. This review examines the current status and direction of our knowledge regarding Ang-II-stimulated signal transduction mechanisms in vascular smooth muscle and cardiac myocytes.
哺乳动物的肾素-血管紧张素系统是一个复杂的、受严格调控的蛋白水解酶和肽产物级联反应系统。其中一个重要的产物血管紧张素 II(Ang-II)是一种循环激素,在许多组织中具有广泛的生理作用,包括心血管系统。众所周知,血管紧张素 II 通过与其特异性受体结合触发多种细胞内反应,增加血管平滑肌和心肌细胞的收缩状态。目前已经了解了这些反应所涉及的一些信号转导机制,而其他机制目前尚未明确。此外,由于肾素-血管紧张素系统与心血管疾病的发生有关,因此最近人们对血管紧张素 II 诱导的信号转导产生了浓厚的兴趣。因此,确定血管紧张素 II 刺激的信号转导机制将阐明正常激素调节心血管稳态的基本原理,以及涉及人类高血压、心律失常和血管损伤或持续压力超负荷后细胞重构等病理过程的基本原理。这篇综述考察了我们目前对血管平滑肌和心肌细胞中血管紧张素 II 刺激的信号转导机制的认识现状和发展方向。