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星形胶质细胞通过 Ca²+-依赖性摄取细胞外 K+来调节神经网络活动。

Astrocytes modulate neural network activity by Ca²+-dependent uptake of extracellular K+.

机构信息

Division of Glia Disease and Therapeutics, Center for Translational Neuromedicine, Department of Neurosurgery, University of Rochester Medical School, Rochester, NY 14640, USA.

出版信息

Sci Signal. 2012 Apr 3;5(218):ra26. doi: 10.1126/scisignal.2002334.

Abstract

Astrocytes are electrically nonexcitable cells that display increases in cytosolic calcium ion (Ca²+) in response to various neurotransmitters and neuromodulators. However, the physiological role of astrocytic Ca²+ signaling remains controversial. We show here that astrocytic Ca²+ signaling ex vivo and in vivo stimulated the Na+,K+-ATPase (Na+- and K+-dependent adenosine triphosphatase), leading to a transient decrease in the extracellular potassium ion (K+) concentration. This in turn led to neuronal hyperpolarization and suppressed baseline excitatory synaptic activity, detected as a reduced frequency of excitatory postsynaptic currents. Synaptic failures decreased in parallel, leading to an increase in synaptic fidelity. The net result was that astrocytes, through active uptake of K+, improved the signal-to-noise ratio of synaptic transmission. Active control of the extracellular K+ concentration thus provides astrocytes with a simple yet powerful mechanism to rapidly modulate network activity.

摘要

星形胶质细胞是电非兴奋细胞,它们会对各种神经递质和神经调质做出细胞浆钙离子(Ca²+)增加的反应。然而,星形胶质细胞 Ca²+信号转导的生理作用仍存在争议。我们在这里展示了星形胶质细胞 Ca²+信号转导在体外和体内刺激了 Na+,K+-ATP 酶(Na+和 K+依赖的三磷酸腺苷酶),导致细胞外钾离子(K+)浓度的短暂下降。这反过来又导致神经元超极化,并抑制了基础兴奋性突触活动,表现为兴奋性突触后电流频率的降低。突触失败率平行下降,导致突触保真度增加。最终结果是,星形胶质细胞通过主动摄取 K+,提高了突触传递的信噪比。因此,对细胞外 K+浓度的主动控制为星形胶质细胞提供了一种简单而强大的机制,可以快速调节网络活动。

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