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  1. 原著論文

Real-Time In Vivo Imaging of Mouse Left Ventricle Reveals Fluctuating Movements of the Intercalated Discs

https://repo.qst.go.jp/records/79477
https://repo.qst.go.jp/records/79477
15380d92-26fe-4da1-8a92-7956ddb909ea
Item type 学術雑誌論文 / Journal Article(1)
公開日 2020-02-03
タイトル
タイトル Real-Time In Vivo Imaging of Mouse Left Ventricle Reveals Fluctuating Movements of the Intercalated Discs
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Fuyu, Kobirumaki-Shimozawa

× Fuyu, Kobirumaki-Shimozawa

WEKO 999954

Fuyu, Kobirumaki-Shimozawa

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Nakanishi, Tomohiro

× Nakanishi, Tomohiro

WEKO 999955

Nakanishi, Tomohiro

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Shimozawa, Togo

× Shimozawa, Togo

WEKO 999956

Shimozawa, Togo

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Terui, Takako

× Terui, Takako

WEKO 999957

Terui, Takako

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Oyama, Kotaro

× Oyama, Kotaro

WEKO 999958

Oyama, Kotaro

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Li, Jia

× Li, Jia

WEKO 999959

Li, Jia

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E. Louch, William

× E. Louch, William

WEKO 999960

E. Louch, William

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Shin’ichi, Ishiwata

× Shin’ichi, Ishiwata

WEKO 999961

Shin’ichi, Ishiwata

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Fukuda, Norio

× Fukuda, Norio

WEKO 999962

Fukuda, Norio

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Kotaro, Oyama

× Kotaro, Oyama

WEKO 999963

en Kotaro, Oyama

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内容記述タイプ Abstract
内容記述 Myocardial contraction is initiated by action potential propagation through the conduction system of the heart. It has been thought that connexin 43 in the gap junctions (GJ) within the intercalated disc (ID) provides direct electric connectivity between cardiomyocytes (electronic conduction). However, recent studies challenge this view by providing evidence that the mechanosensitive cardiac sodium channels Nav1.5 localized in perinexii at the GJ edge play an important role in spreading action potentials between neighboring cells (ephaptic conduction). In the present study, we performed real-time confocal imaging of the CellMask-stained ID in the living mouse heart in vivo. We found that the ID structure was not rigid. Instead, we observed marked flexing of the ID during propagation of contraction from cell to cell. The variation in ID length was between ~30 and ~42 μm (i.e., magnitude of change, ~30%). In contrast, tracking of α-actinin-AcGFP revealed a comparatively small change in the lateral dimension of the transitional junction near the ID (i.e., magnitude of change, ~20%). The present findings suggest that, when the heart is at work, mechanostress across the perinexii may activate Nav1.5 by promoting ephaptic conduction in coordination with electronic conduction, and, thereby, efficiently transmitting excitation-contraction coupling between cardiomyocytes.
書誌情報 Nanomaterials

巻 10, 号 3, p. 532, 発行日 2020-03
出版者
出版者 MDPI
ISSN
収録物識別子タイプ ISSN
収録物識別子 2079-4991
DOI
識別子タイプ DOI
関連識別子 10.3390/nano10030532
関連サイト
識別子タイプ URI
関連識別子 https://www.mdpi.com/2079-4991/10/3/532
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