The Cellular Mechanisms of Neuronal Swelling Underlying Cytotoxic Edema

被引:197
作者
Rungta, Ravi L. [1 ]
Choi, Hyun B. [1 ]
Tyson, John R. [1 ,2 ]
Malik, Aqsa [1 ]
Dissing-Olesen, Lasse [1 ]
Lin, Paulo J. C. [3 ]
Cain, Stuart M. [1 ,2 ]
Cullis, Pieter R. [3 ]
Snutch, Terrance P. [1 ,2 ]
MacVicar, Brian A. [1 ]
机构
[1] Univ British Columbia, Djavad Mowafaghian Ctr Brain Hlth, Vancouver, BC V6T 2B5, Canada
[2] Univ British Columbia, Michael Smith Labs, Vancouver, BC V6T 1Z4, Canada
[3] Univ British Columbia, Dept Biochem & Mol Biol, Vancouver, BC V6T 1Z3, Canada
基金
加拿大健康研究院;
关键词
SPREADING DEPRESSION; CHLORIDE TRANSPORTER; ANION-EXCHANGERS; BRAIN; EXPRESSION; SLC26A11; RELEASE; CALCIUM; SODIUM; NMDA;
D O I
10.1016/j.cell.2015.03.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cytotoxic brain edema triggered by neuronal swelling is the chief cause of mortality following brain trauma and cerebral infarct. Using fluorescence lifetime imaging to analyze contributions of intracellular ionic changes in brain slices, we find that intense Na+ entry triggers a secondary increase in intracellular Cl- that is required for neuronal swelling and death. Pharmacological and siRNA-mediated knockdown screening identified the ion exchanger SLC26A11 unexpectedly acting as a voltage-gated Cl- channel that is activated upon neuronal depolarization to membrane potentials lower than -20 mV. Blockade of SLC26A11 activity attenuates both neuronal swelling and cell death. Therefore cytotoxic neuronal edema occurs when sufficient Na+ influx and depolarization is followed by Cl- entry via SLC26A11. The resultant NaCl accumulation causes subsequent neuronal swelling leading to neuronal death. These findings shed light on unique elements of volume control in excitable cells and lay the ground for the development of specific treatments for brain edema.
引用
收藏
页码:610 / 621
页数:12
相关论文
共 49 条
[1]   Sequential release of GABA by exocytosis and reversed uptake leads to neuronal swelling in simulated ischemia of hippocampal slices [J].
Allen, NJ ;
Rossi, DJ ;
Attwell, D .
JOURNAL OF NEUROSCIENCE, 2004, 24 (15) :3837-3849
[2]   The SLC26 gene family of anion transporters and channels [J].
Alper, Seth L. ;
Sharma, Alok K. .
MOLECULAR ASPECTS OF MEDICINE, 2013, 34 (2-3) :494-515
[3]  
AlvarezLeefmans FJ, 2009, PHYSIOLOGY AND PATHOLOGY OF CHLORIDE TRANSPORTERS AND CHANNELS IN THE NERVOUS SYSTEM: FROM MOLECULES TO DISEASES, P1
[4]   A population-based study of seizures after traumatic brain injuries [J].
Annegers, JF ;
Hauser, WA ;
Coan, SP ;
Rocca, WA .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 338 (01) :20-24
[5]  
[Anonymous], 2012, JASPERS BASIC MECH E
[6]   Presynaptic calcium measurements at physiological temperatures using a new class of dextran-conjugated indicators [J].
Beierlein, M ;
Gee, KR ;
Martin, VV ;
Regehr, WG .
JOURNAL OF NEUROPHYSIOLOGY, 2004, 92 (01) :591-599
[7]   Fluorescence Lifetime Measurements and Biological Imaging [J].
Berezin, Mikhail Y. ;
Achilefu, Samuel .
CHEMICAL REVIEWS, 2010, 110 (05) :2641-2684
[8]   Cation-Chloride Cotransporters and Neuronal Function [J].
Blaesse, Peter ;
Airaksinen, Matti S. ;
Rivera, Claudio ;
Kaila, Kai .
NEURON, 2009, 61 (06) :820-838
[9]   Modular structure of sodium-coupled bicarbonate transporters [J].
Boron, Walter F. ;
Chen, Liming ;
Parker, Mark D. .
JOURNAL OF EXPERIMENTAL BIOLOGY, 2009, 212 (11) :1697-1706
[10]  
CHOI DW, 1987, J NEUROSCI, V7, P369