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  1. H180 生物機能開発利用研究センター
  2. H180a 雑誌掲載論文
  3. 学術雑誌

Analysis of plasmodesmata permeability using cultured tobacco BY-2 cells entrapped in microfluidic chips

http://hdl.handle.net/2237/0002004228
http://hdl.handle.net/2237/0002004228
8ae8f15b-57a3-4a9f-86c7-33b6cf57e2e0
名前 / ファイル ライセンス アクション
openaccess_Kurotani_et_al.pdf openaccess_Kurotani_et_al.pdf (3.9 MB)
 Download is available from 2023/8/31.
Item type itemtype_ver1(1)
公開日 2022-11-29
タイトル
タイトル Analysis of plasmodesmata permeability using cultured tobacco BY-2 cells entrapped in microfluidic chips
言語 en
著者 Kurotani, Ken-ichi

× Kurotani, Ken-ichi

en Kurotani, Ken-ichi

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Kawakatsu, Yaichi

× Kawakatsu, Yaichi

en Kawakatsu, Yaichi

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Kikkawa, Masahiro

× Kikkawa, Masahiro

en Kikkawa, Masahiro

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Tabata, Ryo

× Tabata, Ryo

en Tabata, Ryo

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Kurihara, Daisuke

× Kurihara, Daisuke

en Kurihara, Daisuke

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Honda, Hiroyuki

× Honda, Hiroyuki

en Honda, Hiroyuki

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Shimizu, Kazunori

× Shimizu, Kazunori

en Shimizu, Kazunori

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Notaguchi, Michitaka

× Notaguchi, Michitaka

en Notaguchi, Michitaka

Search repository
アクセス権
アクセス権 embargoed access
アクセス権URI http://purl.org/coar/access_right/c_f1cf
権利
言語 en
権利情報 This version of the article has been accepted for publication, after peer review (when applicable) and is subject to Springer Nature’s AM terms of use, but is not the Version of Record and does not reflect post-acceptance improvements, or any corrections. The Version of Record is available online at: http://dx.doi.org/10.1007/s10265-022-01406-8
内容記述
内容記述 Plasmodesmata are unique channel structures in plants that link the fluid cytoplasm between adjacent cells. Plants have evolved these microchannels to allow trafficking of nutritious substances as well as regulatory factors for intercellular communication. However, tracking the behavior of plasmodesmata in real time is difficult because they are located inside tissues. Hence, a system was constructed to monitor the movement of substances by plasmodesmata using tobacco BY-2 cells, which are linearly organized cells, and a microfluidic device that traps them in place and facilitates observation. After targeting one cell for photobleaching, recovery of the lost H2B-GFP protein was detected within 200 min. No recovery was detected in that time frame by photobleaching the entire cell filaments. This suggested that the recovery of H2B-GFP protein was not due to de novo protein synthesis, but rather to translocation from neighboring cells. The transport of H2B-GFP protein was not observed when sodium chloride, a compound known to cause plasmodesmata closure, was present in the microfluid channel. Thus, using the microfluidic device and BY-2 cells, it was confirmed that the behavior of plasmodesmata could be observed in real time under controllable conditions.
言語 en
内容記述タイプ Abstract
出版者
言語 en
出版者 Springer Nature
言語
言語 eng
資源タイプ
資源タイプresource http://purl.org/coar/resource_type/c_6501
タイプ journal article
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
関連情報
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1007/s10265-022-01406-8
収録物識別子
収録物識別子タイプ PISSN
収録物識別子 0918-9440
書誌情報 en : Journal of Plant Research

巻 135, 号 5, p. 693-701, 発行日 2022-09
ファイル公開日
日付 2023-09-01
日付タイプ Available
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