Wang D, Martens J R, Posner P, Sumners C, Gelband C H
Department of Physiology, University of Florida College of Medicine, Gainesville 32610, USA.
J Neurochem. 1996 Sep;67(3):996-1004. doi: 10.1046/j.1471-4159.1996.67030996.x.
This study examines the angiotensin II (Ang II) regulation of intracellular free calcium concentration ([Ca2+]i) in astroglia cultured from the hypothalamus and brainstem of the adult rat. Bath perfusion or rapid puffer application of angiotensin II (Ang II) (1-100 nM) increased [Ca2+]i in both polygonal and stellate astroglia when measured using fura-2 imaging fluorescence microscopy. Ang II increased [Ca2+]i in 96.1 and 95.6% of the polygonal and stellate glial cells, respectively. In normal Tyrode's solution (containing 2 mM CaCl2), the Ang II-stimulated increase in [Ca2+]i characteristically showed a biphasic response, i.e., an initial rapid transient peak followed by a sustained, steady-state plateau of free Ca2+. In both cell types, the selective Ang II type 1 receptor subtype (AT1) antagonist losartan (1 microM) inhibited the Ang II-stimulated increase in [Ca2+]i. The selective AT2 antagonist PD 123319 (1 microM) did not inhibit the Ang II-stimulated increase in [Ca2+]i in either cell type. To define the sources of Ca2+ that participate in the Ang II-stimulated increase in [Ca2+]i in astroglia, experiments were performed in a nominally Ca(2+)-free Tyrode's solution. In either cell type, this resulted in only an initial transient increase of Ca2+ and no sustained plateau of Ca2+ when challenged with Ang II. Thapsigargin (5 microM), cyclopiazonic acid (10 microM), and ryanodine (10 microM), but not caffeine (1-10 mM), inhibited the initial rise in [Ca2+]i. The plateau increase of [Ca2+]i caused by Ang II (100 nM) was reversibly inhibited by both cadmium (100 microM) and nifedipine (10 microM); in contrast, gadolinium (100 microM) had no effect on the plateau increase of [Ca2+]i. These results indicate that Ang II, in physiological concentrations, can activate AT1 receptors to stimulate both Ca2+ release from intracellular stores and Ca2+ influx from the extracellular space to increase [Ca2+]i of polygonal and stellate astroglia.
本研究检测了成年大鼠下丘脑和脑干培养的星形胶质细胞中血管紧张素II(Ang II)对细胞内游离钙浓度([Ca2+]i)的调节作用。当使用fura-2成像荧光显微镜测量时,通过浴槽灌注或快速喷射应用血管紧张素II(Ang II)(1 - 100 nM)可使多角形和星形胶质细胞中的[Ca2+]i升高。Ang II分别使96.1%的多角形胶质细胞和95.6%的星形胶质细胞中的[Ca2+]i升高。在正常的台氏液(含2 mM CaCl2)中,Ang II刺激引起的[Ca2+]i升高表现出双相反应,即最初的快速瞬态峰值,随后是游离钙的持续稳态平台期。在两种细胞类型中,选择性血管紧张素II 1型受体亚型(AT1)拮抗剂氯沙坦(1 microM)可抑制Ang II刺激引起的[Ca2+]i升高。选择性AT2拮抗剂PD 123319(1 microM)在两种细胞类型中均未抑制Ang II刺激引起的[Ca2+]i升高。为了确定参与Ang II刺激星形胶质细胞中[Ca2+]i升高的钙来源,在名义上无钙的台氏液中进行了实验。在两种细胞类型中,当用Ang II刺激时,这仅导致钙的初始瞬态升高,而没有钙的持续平台期。毒胡萝卜素(5 microM)、环匹阿尼酸(10 microM)和ryanodine(10 microM)可抑制[Ca2+]i的初始升高,但咖啡因(1 - 10 mM)则无此作用。Ang II(100 nM)引起的[Ca2+]i平台期升高可被镉(100 microM)和硝苯地平(10 microM)可逆性抑制;相比之下,钆(100 microM)对[Ca2+]i的平台期升高无影响。这些结果表明,生理浓度的Ang II可激活AT1受体,刺激细胞内钙库释放钙以及细胞外钙内流,从而增加多角形和星形胶质细胞中的[Ca2+]i。