Neuronal pannexin-1 channels are not molecular routes of water influx during spreading depolarization-induced dendritic beading

被引:18
作者
Sword, Jeremy [1 ]
Croom, Deborah [1 ]
Wang, Phil L. [1 ]
Thompson, Roger J. [2 ]
Kirov, Sergei A. [1 ,3 ]
机构
[1] Med Coll Georgia, Brain & Behav Discovery Inst, Augusta, GA 30912 USA
[2] Univ Calgary, Hotchkiss Brain Inst, Dept Cell Biol & Anat, Calgary, AB, Canada
[3] Med Coll Georgia, Dept Neurosurg, Augusta, GA 30912 USA
基金
美国国家卫生研究院;
关键词
Conditional pannexin-1 knock-out; mefloquine; neuronal swelling; two-photon imaging; viral vectors; IN-VIVO; CELLULAR-LOCALIZATION; NERVOUS-SYSTEM; LASER SPECKLE; MOUSE CORTEX; HEMICHANNELS; DEPRESSION; CALCIUM; ACTIVATION; ISCHEMIA;
D O I
10.1177/0271678X16639328
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Spreading depolarization-induced focal dendritic swelling (beading) is an early hallmark of neuronal cytotoxic edema. Pyramidal neurons lack membrane-bound aquaporins posing a question of how water enters neurons during spreading depolarization. Recently, we have identified chloride-coupled transport mechanisms that can, at least in part, participate in dendritic beading. Yet transporter-mediated ion and water fluxes could be paralleled by water entry through additional pathways such as large-pore pannexin-1 channels opened by spreading depolarization. Using real-time in vivo two-photon imaging in mice with pharmacological inhibition or conditional genetic deletion of pannexin-1, we showed that pannexin-1 channels are not required for spreading depolarization-induced focal dendritic swelling.
引用
收藏
页码:1626 / 1633
页数:8
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