Rossier M F, Capponi A M
Department of Internal Medicine, University Hospital, Geneva, Switzerland.
Vitam Horm. 2000;60:229-84. doi: 10.1016/s0083-6729(00)60021-3.
Sixty years after its initial discovery, the octapeptide hormone angiotensin II (AngII) has proved to play numerous physiological roles that reach far beyond its initial description as a hypertensive factor. In spite of the host of target tissues that have been identified, only two major receptor subtypes, AT1 and AT2, are currently fully identified. The specificity of the effects of AngII relies upon numerous and complex intracellular signaling pathways that often mobilize calcium ions from intracellular stores or from the extracellular medium. Various types of calcium channels (store- or voltage-operated channels) endowed with distinct functional properties play a crucial role in these processes. The activity of these channels can be modulated by AngII in a positive and/or negative fashion, depending on the cell type under observation. This chapter reviews the main characteristics of AngII receptor subtypes and of the various calcium channels as well as the involvement of the multiple signal transduction mechanisms triggered by the hormone in the cell-specific modulation of the activity of these channels.
八肽激素血管紧张素II(AngII)首次被发现60年后,已证明它发挥着众多生理作用,其作用范围远远超出了最初作为一种高血压因子的描述。尽管已确定了许多靶组织,但目前仅完全鉴定出两种主要受体亚型,即AT1和AT2。AngII作用的特异性依赖于众多复杂的细胞内信号通路,这些信号通路常常从细胞内储存库或细胞外介质中动员钙离子。具有不同功能特性的各种类型的钙通道(储存或电压门控通道)在这些过程中起着至关重要的作用。根据所观察的细胞类型,AngII可以以正向和/或负向方式调节这些通道的活性。本章综述了AngII受体亚型和各种钙通道的主要特征,以及该激素触发的多种信号转导机制在这些通道活性的细胞特异性调节中的作用。