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  Calcium channel types with distinct presynaptic localization couple differentially to transmitter release in single calyx-type synapses

Wu, L.-G., Westenbroek, R. E., Borst, J. G. G., Catterall, W. A., & Sakmann, B. (1999). Calcium channel types with distinct presynaptic localization couple differentially to transmitter release in single calyx-type synapses. The Journal of Neuroscience, 19, 726-736. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/9880593.

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資料種別: 学術論文
その他のタイトル : Calcium channel types with distinct presynaptic localization couple differentially to transmitter release in single calyx-type synapses

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JNeurosci_19_1999_726.pdf (全文テキスト(全般)), 520KB
 
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JNeurosci_19_1999_726.pdf
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 作成者:
Wu, Ling-Gang1, 著者           
Westenbroek, Ruth E., 著者
Borst, J. Gerard G.1, 著者           
Catterall, William A., 著者
Sakmann, Bert1, 著者           
所属:
1Department of Cell Physiology, Max Planck Institute for Medical Research, Max Planck Society, ou_1497701              

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キーワード: Ca21 channels; presynaptic; calyx of Held; voltage clamp; antibody; immunocytochemistry; P-type Ca21 channels; N-type Ca21 channels; R-type Ca21 channels; synaptotagmin; fura-2; rat
 要旨: We studied how Ca2+ influx through different subtypes of Ca2+ channels couples to release at a calyx-type terminal in the rat medial nucleus of the trapezoid body by simultaneously measuring the presynaptic Ca2+ influx evoked by a single action potential and the EPSC. Application of subtype-specific toxins showed that Ca2+ channels of the P/Q-, N-, and R-type controlled glutamate release at a single terminal. The Ca2+influx through the P/Q-type channels triggered release more effectively than Ca2+ influx through N- or R-type channels. We investigated mechanisms that contributed to these differences in effectiveness. Electrophysiological experiments suggested that individual release sites were controlled by all three subtypes of Ca2+ channels. Immunocytochemical staining indicated, however, that a substantial fraction of N- and R-type channels was located distant from release sites. Although these distant channels contributed to the Ca2+ influx into the terminal, they may not contribute to release. Taken together, the results suggest that the Ca2+ influx into the calyx via N- and R-type channels triggers release less effectively than that via P/Q-type because a substantial fraction of the N- and R-type channels in the calyx is localized distant from release sites

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言語: eng - English
 日付: 1998-10-281998-08-191998-10-291999-01-15
 出版の状態: 出版
 ページ: 11
 出版情報: -
 目次: -
 査読: 査読あり
 識別子(DOI, ISBNなど): eDoc: 666520
URI: http://www.ncbi.nlm.nih.gov/pubmed/9880593
URI: http://www.jneurosci.org/content/19/2/726.full
その他: 4495
 学位: -

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出版物 1

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出版物名: The Journal of Neuroscience
  その他 : J. Neurosci.
種別: 学術雑誌
 著者・編者:
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出版社, 出版地: Baltimore, MD : The Society
ページ: - 巻号: 19 通巻号: - 開始・終了ページ: 726 - 736 識別子(ISBN, ISSN, DOIなど): ISSN: 0270-6474
CoNE: https://pure.mpg.de/cone/journals/resource/954925502187