Glial Nax channels control lactate signaling to neurons for brain [Na+] sensing

被引:161
作者
Shimizu, Hidetada
Watanabe, Eiji
Hiyama, Takeshi Y.
Nagakura, Ayano
Fujikawa, Akihiro
Okado, Haruo
Yanagawa, Yuchio
Obata, Kunihiko
Noda, Masaharu [1 ]
机构
[1] Natl Inst Basic Biol, Div Mol Neurobiol, Okazaki, Aichi 4448787, Japan
[2] Natl Inst Basic Biol, Lab Neurophysiol, Okazaki, Aichi 4448787, Japan
[3] Grad Univ Adv Studies, Sch Life Sci, Okazaki, Aichi 4448787, Japan
[4] Tokyo Metropolitan Inst Neurosci, Dept Mol Physiol, Fuchu, Tokyo 1838526, Japan
[5] Gunma Univ, Dept Genet & Behav Neurosci, Grad Sch Med, Maebashi, Gunma 3718511, Japan
[6] RIKEN, Neuronal Circuit Mechanisms Res Grp, Brain Sci Inst, Wako, Saitama 3510198, Japan
关键词
D O I
10.1016/j.neuron.2007.03.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sodium (Na) homeostasis is crucial for life, and Na levels in body fluids are constantly monitored in the brain. The subfornical organ (SFO) is the center of the sensing responsible for the control of salt-intake behavior, where Na-x channels are expressed in specific glial cells as the Na-level sensor. Here, we show direct interaction between Na-x channels and alpha subunits of Na+/K+-ATPase, which brings about Na-dependent activation of the metabolic state of the glial cells. The metabolic enhancement leading to extensive lactate production was observed in the SFO of wild-type mice, but not of the Na-x-knockout mice. Furthermore, lactate, as well as Na, stimulated the activity of GABAergic neurons in the SFO. These results suggest that the information on a physiological increase of the Na level in body fluids sensed by Na-x in glial cells is transmitted to neurons by lactate as a mediator to regulate neural activities of the SFO.
引用
收藏
页码:59 / 72
页数:14
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