Simard Marie, Arcuino Gregory, Takano Takahiro, Liu Qing Song, Nedergaard Maiken
Department of Neurosurgery, New York Medical College, Valhalla, New York 10590, USA.
J Neurosci. 2003 Oct 8;23(27):9254-62. doi: 10.1523/JNEUROSCI.23-27-09254.2003.
Advances in fluorescent calcium indicating dyes over the past decade have identified calcium signaling as the tool by which astrocytes communicate among themselves and with neighboring neurons. Studies of astrocyte-neuron interactions have shown that calcium signaling is a potent modulator of the strength of both excitatory and inhibitory synapses. The concept that astrocytes possess a mechanism for rapid cell communication has not been incorporated, however, into the supportive functions of astrocytes. Because many of the classical tasks of astrocytes are linked to the blood-brain barrier, we have here examined the expression of proteins required for calcium signaling in their vascular end-foot processes. The gap junction protein, Cx43, was expressed intensively around the vessels interconnecting astrocytic end-foot processes. These gap junctions permitted diffusion of Lucifer yellow, specifically along the path of glial end feet apposed to the vessel wall. The purinergic receptors, P2Y(2) and P2Y(4), were also strongly expressed at the gliovascular interface and colocalized with GFAP around larger vessels in cortex. Multiphoton imaging of freshly prepared brain slices loaded with Fluo-4/AM revealed that ATP mobilized cytosolic calcium in astrocytic end feet, whereas electrical stimulation triggered calcium waves propagating along the vessel wall. Brain endothelial cells and pericytes were physically separated from astrocytes by the basal lamina and responded only weakly to ATP. These observations identify astrocytic end-foot processes plastered at the vessel wall as a center for purinergic signaling. It is speculated that calcium signaling may play a role in astrocytic functions related to the blood-brain barrier, including blood flow regulation, metabolic trafficking, and water homeostasis.
在过去十年中,荧光钙指示染料的进展已将钙信号识别为星形胶质细胞之间以及与相邻神经元进行通信的工具。对星形胶质细胞 - 神经元相互作用的研究表明,钙信号是兴奋性和抑制性突触强度的有效调节因子。然而,星形胶质细胞具有快速细胞通信机制的概念尚未纳入星形胶质细胞的支持功能中。由于星形胶质细胞的许多经典任务都与血脑屏障相关,我们在此研究了其血管终足过程中钙信号所需蛋白质的表达。缝隙连接蛋白Cx43在连接星形胶质细胞终足过程的血管周围大量表达。这些缝隙连接允许荧光黄扩散,特别是沿着与血管壁相邻的胶质终足路径扩散。嘌呤能受体P2Y(2)和P2Y(4)在胶质血管界面也强烈表达,并与皮质中较大血管周围的GFAP共定位。对加载有Fluo-4/AM的新鲜制备脑切片进行多光子成像显示,ATP可动员星形胶质细胞终足中的胞质钙,而电刺激则触发沿血管壁传播的钙波。脑内皮细胞和周细胞通过基膜与星形胶质细胞物理分离,并且对ATP的反应较弱。这些观察结果表明,贴附在血管壁上的星形胶质细胞终足过程是嘌呤能信号传导的中心。据推测,钙信号可能在与血脑屏障相关的星形胶质细胞功能中发挥作用,包括血流调节、代谢运输和水平衡。