Concurrent observations of astrocytic Ca2+ activity and multisite extracellular potentials from an intact cerebral cortex

被引:7
作者
Riera, Jorge [1 ]
Ogawa, Takeshi [1 ]
Hatanaka, Rieko [1 ]
Goto, Takakuni [1 ]
Sumiyoshi, Akira [1 ]
Kadji, Herve Enjieu [1 ]
Nakauchi, Sakura [1 ]
Kawashima, Ryuta [1 ]
机构
[1] Tohoku Univ, IDAC, Aoba Ku, Sendai, Miyagi 9808575, Japan
关键词
neurovascular coupling; neuronal modulation; multiscale cellular activity; LFP/MUA; two-photon laser scanning microscopy; CALCIUM DYNAMICS; NETWORKS; RECEPTORS; MODEL;
D O I
10.1002/jbio.200910036
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In basic neuroscience, the attention has been recently focused on the role played by the protoplasmic astrocytes in modulating the activity of nearby neurons or else on assisting a long-term/sustained communication between these neurons and the surrounding microvasculature. However, to understand the physiological mechanisms underlying such a multiscale interactions in space and time, novel methodologies are required. This paper reports about an experimental setting and a procedure that was developed to obtain concurrently two-photon astrocytic Ca2+ imaging and multisite large-scale extracellular potentials as recorded by a silicon-based probe. Solutions to several technical drawbacks (e.g. removal of photoelectric artifacts, the establishment of safety ranges for microinjection) are provided which are intrinsic to the technology and procedure utilized. Through the use of SR101 to stain protoplasmic astrocytes, it was possible to combine functional information represented by the Ca2+ activity in individual astrocytes and the LFPs with geometrical descriptors of the astrocytic/vessel networks. (C) 2010 by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
引用
收藏
页码:147 / 160
页数:14
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