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Ca2+ wave as a regulatory message tool for cellular communication

https://repo.qst.go.jp/records/77899
https://repo.qst.go.jp/records/77899
dc088ace-d4a0-4edb-8ed0-ba8f28548b91
Item type 会議発表用資料 / Presentation(1)
公開日 2019-11-25
タイトル
タイトル Ca2+ wave as a regulatory message tool for cellular communication
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_c94f
資源タイプ conference object
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 Suzuki, Ami

× Suzuki, Ami

WEKO 860322

Suzuki, Ami

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Yokoya, Akinari

× Yokoya, Akinari

WEKO 860323

Yokoya, Akinari

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Suzuki, Ami

× Suzuki, Ami

WEKO 860324

en Suzuki, Ami

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Yokoya, Akinari

× Yokoya, Akinari

WEKO 860325

en Yokoya, Akinari

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抄録
内容記述タイプ Abstract
内容記述 Waves of concentration change of specific signal molecules play an important role in signal exchanges between cells. To response to stimulus from outside of the cellular system they might communicate each other using waves. In this study, we focus on Ca2+ functioning as second messenger within cells. Normally, Ca2+ are stored in endoplasmic reticulum (ER). In response to the environmental stimulus, the Ca2+ channels on the ER membrane could be gated and induce a repetition of temporary ups and downs of the Ca2+ concentration in a cell. This “wave”, so-called Ca2+ concentration oscillation, has been predicted to regulate various physiological functions in cells. We investigate whether this temporal oscillation arises when cells are exposed to ionizing radiation. In this study, first, we tried to establish a measurement technique to visualize the Ca2+ concentration in mammalian cells. Normal human fibroblast cells were treated with a Ca2+ specific chemical fluorescent probe, Fluo 4. Then live-cell observations were performed with a fluorescent microscope to obtain time-lapse movies. Fluorescent intensities of the cells at each time point were converted to relative values to that at the beginning time of observation. Slight changes of the fluorescence in the most cells were recognized. Furthermore, some cells transiently showed intensive ups and downs of their fluorescence, indicating the occurrence of the Ca2+ waves. Using this method, for the next step, we challenge to detect local Ca2+ concentration oscillation in cell nucleus or organelle after exposure of ionizing radiation.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 第3回QST国際シンポジウム「Quantum Life Science」
発表年月日
日付 2019-12-04
日付タイプ Issued
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