Receptor-mediated glutamate release from volume sensitive channels in astrocytes

被引:165
作者
Takano, T
Kang, J
Jaiswal, JK
Simon, SM
Lin, JHC
Yu, YF
Li, YX
Yang, J
Dienel, G
Zielke, HR
Nedergaard, M
机构
[1] Univ Rochester, Med Ctr, Ctr Aging & Dev Biol, Rochester, NY 14642 USA
[2] New York Med Coll, Dept Cell Biol, Valhalla, NY 10595 USA
[3] New York Med Coll, Dept Pathol, Valhalla, NY 10595 USA
[4] Rockefeller Univ, Lab Cellular Biophys, New York, NY 10021 USA
[5] Columbia Univ, Coll Phys & Surg, Dept Anesthesiol, New York, NY 10032 USA
[6] Univ Arkansas Med Sci, Dept Neurol, Little Rock, AR 72205 USA
[7] Univ Maryland, Dept Pediat, Baltimore, MD 21201 USA
关键词
electrophysiology; exocytosis; neurotransmitters; osmolarity; synapses;
D O I
10.1073/pnas.0506382102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Several lines of work have shown that astrocytes release glutamate in response to receptor activation, which results in a modulation of local synaptic activity. Astrocytic glutamate release is Ca2+-dependent and occurs in conjunction with exocytosis of glutamate containing vesicles. However, astrocytes contain a millimolar concentration of cytosolic glutamate and express channels permeable to small anions, such as glutamate. Here, we tested the idea that astrocytes respond to receptor stimulation by dynamic changes in cell volume, resulting in volume-sensitive channel activation, and efflux of cytosolic glutamate. Confocal imaging and whole-cell recordings demonstrated that astrocytes exhibited a transient Ca2+-dependent cell volume increase, which activated glutamate permeable channels. HPLC analysis revealed that glutamate was released in conjunction with other amino acid os-molytes. Our observations indicate that volume-sensitive channel may constitute a previously uncharacterized target for modulation of astrocyte-neuronal interactions.
引用
收藏
页码:16466 / 16471
页数:6
相关论文
共 30 条
[1]   Astrocytes contain a vesicular compartment that is competent for regulated exocytosis of glutamate [J].
Bezzi, P ;
Gundersen, V ;
Galbete, JL ;
Seifert, G ;
Steinhäuser, C ;
Pilati, E ;
Volterra, A .
NATURE NEUROSCIENCE, 2004, 7 (06) :613-620
[2]   Prostaglandins stimulate calcium-dependent glutamate release in astrocytes [J].
Bezzi, P ;
Carmignoto, G ;
Pasti, L ;
Vesce, S ;
Rossi, D ;
Rizzini, BL ;
Pozzan, T ;
Volterra, A .
NATURE, 1998, 391 (6664) :281-285
[3]   Connexins regulate calcium signaling by controlling ATP release [J].
Cotrina, ML ;
Lin, JHC ;
Alves-Rodrigues, A ;
Liu, S ;
Li, J ;
Azmi-Ghadimi, H ;
Kang, J ;
Naus, CCG ;
Nedergaard, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15735-15740
[4]   P2X7 receptor-mediated release of excitatory amino acids from astrocytes [J].
Duan, SM ;
Anderson, CM ;
Keung, EC ;
Chen, YM ;
Chen, YR ;
Swanson, RA .
JOURNAL OF NEUROSCIENCE, 2003, 23 (04) :1320-1328
[5]   Monte Carlo simulation of vesicular release, spatiotemporal distribution of glutamate in synaptic cleft and generation of postsynaptic currents [J].
Glavinovic, MI .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1999, 437 (03) :462-470
[6]  
HANSSON E, 1994, J BIOL CHEM, V269, P21955
[7]   Glia: Listening and talking to the synapse [J].
Haydon, PG .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (03) :185-193
[8]   Molecular structure and physiological function of chloride channels [J].
Jentsch, TJ ;
Stein, V ;
Weinreich, F ;
Zdebik, AA .
PHYSIOLOGICAL REVIEWS, 2002, 82 (02) :503-568
[9]   Astrocyte-mediated potentiation of inhibitory synaptic transmission [J].
Kang, J ;
Jiang, L ;
Goldman, SA ;
Nedergaard, M .
NATURE NEUROSCIENCE, 1998, 1 (08) :683-692
[10]  
KANG J, 1999, IMAGING ASTROCYTES A