Glial calcium: Homeostasis and signaling function

被引:561
作者
Verkhratsky, A [1 ]
Orkand, RK
Kettenmann, H
机构
[1] Max Delbruck Ctr Mol Med, Dept Cellular Neurosci, Berlin, Germany
[2] Univ Puerto Rico, Inst Neurobiol, San Juan, PR 00901 USA
关键词
D O I
10.1152/physrev.1998.78.1.99
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Glial cells respond to various electrical, mechanical, and chemical stimuli, including neurotransmitters, neuromodulators, and hormones, with an increase in intracellular Ca2+ concentration ([Ca2+](i)). The increases exhibit a variety of temporal and spatial patterns. These [Ca2+](i) responses result from the coordinated activity of a number of molecular cascades responsible for Ca2+ movement into or out of the cytoplasm either by way of the extracellular space or intracellular stores. Transplasmalemmal Ca2+ movements may be controlled by several types of voltage-and ligand-gated Ca2+-permeable channels as well as Ca2+ pumps and a Na+/Ca2+ exchanger. In addition, glial cells express various metabotropic receptors coupled to intracellular Ca2+ stores through the intracellular messenger inositol 1,4,5-trisphosphate. The interplay of different molecular cascades enables the development of agonist-specific patterns of Ca2+ responses. Such agonist specificity may provide a means for intracellular and intercellular information coding. Calcium signals can traverse gal, junctions between glial cells without decrement. These waves can serve as a substrate for integration of glial activity. By controlling gap junction conductance, Ca2+ waves may define the limits of functional glial networks. Neuronal activity can trigger [Ca2+](i) signals in apposed glial cells, and moreover, there is some evidence that glial [Ca2+](i) waves can affect neurons. Glial Ca2+ signaling can be regarded as a form of glial excitability.
引用
收藏
页码:99 / 141
页数:43
相关论文
共 465 条
[1]   GLUTAMATE STIMULATES RELEASE OF CA-2+ FROM INTERNAL STORES IN ASTROGLIA [J].
AHMED, Z ;
LEWIS, CA ;
FABER, DS .
BRAIN RESEARCH, 1990, 516 (01) :165-169
[2]  
Akopian G, 1996, GLIA, V17, P181
[3]   EVIDENCE FOR AN INTERACTION BETWEEN GABA-B AND GLUTAMATE RECEPTORS IN ASTROCYTES AS REVEALED BY CHANGES IN CA-2+ FLUX [J].
ALBRECHT, J ;
PEARCE, B ;
MURPHY, S .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1986, 125 (03) :463-464
[4]   ATP ACTIVATES CATIONIC AND ANIONIC CONDUCTANCES IN SCHWANN-CELLS CULTURED FROM DORSAL-ROOT GANGLIA OF THE MOUSE [J].
AMEDEE, T ;
DESPEYROUX, S .
PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1995, 259 (1356) :277-284
[5]   VOLTAGE-DEPENDENT CALCIUM AND POTASSIUM CHANNELS IN SCHWANN-CELLS CULTURED FROM DORSAL-ROOT GANGLIA OF THE MOUSE [J].
AMEDEE, T ;
ELLIE, E ;
DUPOUY, B ;
VINCENT, JD .
JOURNAL OF PHYSIOLOGY-LONDON, 1991, 441 :35-56
[6]  
Amundson J, 1993, Curr Opin Neurobiol, V3, P375, DOI 10.1016/0959-4388(93)90131-H
[7]   STIMULATION OF PHOSPHOINOSITIDE HYDROLYSIS BY SEROTONIN IN C6 GLIOMA-CELLS [J].
ANANTH, US ;
LELI, U ;
HAUSER, G .
JOURNAL OF NEUROCHEMISTRY, 1987, 48 (01) :253-261
[8]   MUSCARINIC RECEPTOR PROFILES OF MOUSE-BRAIN ASTROCYTES IN CULTURE VARY WITH THEIR TISSUE OF ORIGIN BUT DIFFER FROM THOSE OF NEURONS [J].
ANDRE, C ;
DOSSANTOS, G ;
KOULAKOFF, A .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1994, 6 (11) :1702-1709
[9]   Extracellular ATP increases intracellular calcium in cultured adult Schwann cells [J].
Ansselin, AD ;
Davey, DF ;
Allen, DG .
NEUROSCIENCE, 1997, 76 (03) :947-955
[10]   HISTAMINE H-1-RECEPTORS MEDIATE PHOSPHOINOSITIDE HYDROLYSIS IN ASTROCYTE-ENRICHED PRIMARY CULTURES [J].
ARBONES, L ;
PICATOSTE, F ;
GARCIA, A .
BRAIN RESEARCH, 1988, 450 (1-2) :144-152