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  Robustness of sensory-evoked excitation is increased by inhibitory inputs to distal apical tuft dendrites

Egger, R., Schmitt, A. C., Wallace, D. J., Sakmann, B., Oberlaender, M., & Kerr, J. N. D. (2015). Robustness of sensory-evoked excitation is increased by inhibitory inputs to distal apical tuft dendrites. Proceedings of the National Academy of Sciences, 112(45), 14072-14077.

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資料種別: 学術論文

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http://www.pnas.org/content/112/45/14072 (全文テキスト(全般))
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 作成者:
Egger, Robert1, 著者
Schmitt, Arno C.1, 著者
Wallace, Damian J.2, 著者
Sakmann, Bert3, 著者
Oberlaender, Marcel3, 著者
Kerr, Jason N. D.2, 著者
所属:
1Max Planck Institute for Biological Cybernetics, Max Planck Society, Spemannstrasse 38, 72076 Tübingen, DE, ou_1497794              
2Center of Advanced European Studies and Research (caesar), Max Planck Society, Ludwig-Erhard-Allee 2, 53175 Bonn, DE, ou_2173675              
3Max Planck Florida Institute for Neuroscience, Max Planck Society, One Max Planck Way, Jupiter FL 33458, USA, ou_1950288              

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キーワード: Barrel cortex cortical column layer 1 NMDAR shunting
 要旨: Cortical inhibitory interneurons (INs) are subdivided into a variety of morphologically and functionally specialized cell types. How the respective specific properties translate into mechanisms that regulate sensory-evoked responses of pyramidal neurons (PNs) remains unknown. Here, we investigated how INs located in cortical layer 1 (L1) of rat barrel cortex affect whisker-evoked responses of L2 PNs. To do so we combined in vivo electrophysiology and morphological reconstructions with computational modeling. We show that whisker-evoked membrane depolarization in L2 PNs arises from highly specialized spatiotemporal synaptic input patterns. Temporally L1 INs and L2–5 PNs provide near synchronous synaptic input. Spatially synaptic contacts from L1 INs target distal apical tuft dendrites, whereas PNs primarily innervate basal and proximal apical dendrites. Simulations of such constrained synaptic input patterns predicted that inactivation of L1 INs increases trial-to-trial variability of whisker-evoked responses in L2 PNs. The in silico predictions were confirmed in vivo by L1-specific pharmacological manipulations. We present a mechanism—consistent with the theory of distal dendritic shunting—that can regulate the robustness of sensory-evoked responses in PNs without affecting response amplitude or latency.

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 日付: 2015-11-10
 出版の状態: 出版
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出版物名: Proceedings of the National Academy of Sciences
種別: 学術雑誌
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出版社, 出版地: -
ページ: - 巻号: 112 (45) 通巻号: - 開始・終了ページ: 14072 - 14077 識別子(ISBN, ISSN, DOIなど): -