SrasV1, Main, Merge, bibRecord, 000D33

Imaging membrane potential changes from dendritic spines using computer-generated holography

Identifieur interne : 000D33 ( Main/Merge ); précédent : 000D32; suivant : 000D34

Imaging membrane potential changes from dendritic spines using computer-generated holography

Auteurs : Dimitrii Tanese [France] ; Ju-Yun Weng [France] ; Valeria Zampini [France] ; Vincent De Sars [France] ; Marco Canepari [France] ; Balazs Rozsa ; Valentina Emiliani [France] ; Dejan Zecevic [États-Unis]

Source :

Neurophotonics [ 2329-423X ] ; 2017-07-01.

RBID : Hal:hal-01872740
Url:

DOI: 10.1117/1.NPh.4.3.031211

Links toward previous steps (curation, corpus...)

to stream Hal, to step Corpus: 000084
to stream Hal, to step Curation: 000084
to stream Hal, to step Checkpoint: 000052
to stream Hal, to step Corpus: 000085
to stream Hal, to step Curation: 000085
to stream Hal, to step Checkpoint: 000051

Links to Exploration step

Hal:hal-01872740

Le document en format XML

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<author><name sortKey="Canepari, Marco" sort="Canepari, Marco" uniqKey="Canepari M" first="Marco" last="Canepari">Marco Canepari</name>
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          <orgName>Centre National de la Recherche Scientifique</orgName>
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<tutelle active="#struct-445543" type="direct"><org type="institution" xml:id="struct-445543" status="VALID">          <idno type="IdRef">188399275</idno>
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          <date type="end">2015-12-31</date>
          <desc>            <address>              <addrLine>BP 53 - 38041 Grenoble Cedex 9</addrLine>
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<country>France</country>
<placeName><settlement type="city">Grenoble</settlement>
<region type="region" nuts="2">Auvergne-Rhône-Alpes</region>
<region type="old region" nuts="2">Rhône-Alpes</region>
</placeName>
<orgName type="university">Université Grenoble-Alpes</orgName>
<placeName><settlement type="city">Grenoble</settlement>
<region type="region" nuts="2">Auvergne-Rhône-Alpes</region>
<region type="old region" nuts="2">Rhône-Alpes</region>
</placeName>
<orgName type="university">Université Joseph Fourier</orgName>
<orgName type="institution" wicri:auto="newGroup">Université de Grenoble</orgName>
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<author><name sortKey="Rozsa, Balazs" sort="Rozsa, Balazs" uniqKey="Rozsa B" first="Balazs" last="Rozsa">Balazs Rozsa</name>
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<country>Hongrie</country>
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<author><name sortKey="Emiliani, Valentina" sort="Emiliani, Valentina" uniqKey="Emiliani V" first="Valentina" last="Emiliani">Valentina Emiliani</name>
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          <orgName>Laboratoire de Neurophotonique</orgName>
          <orgName type="acronym">UMR 8250</orgName>
          <date type="start">2014-01-01</date>
          <date type="end">2018-12-31</date>
          <desc>            <address>              <addrLine>Faculté des Sciences Fondamentales et Biomédicales45, rue des Saints Pères 75270 Paris Cedex 06</addrLine>
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          <orgName>Centre National de la Recherche Scientifique</orgName>
          <orgName type="acronym">CNRS</orgName>
          <date type="start">1939-10-19</date>
          <desc>            <address>              <country key="FR"></country>
            </address>
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          </desc>
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</tutelles>
</hal:affiliation>
<country>France</country>
</affiliation>
</author>
<author><name sortKey="Zecevic, Dejan" sort="Zecevic, Dejan" uniqKey="Zecevic D" first="Dejan" last="Zecevic">Dejan Zecevic</name>
<affiliation wicri:level="1"><hal:affiliation type="laboratory" xml:id="struct-208247" status="INCOMING">          <orgName>Department of Cellular and Molecular Physiology</orgName>
          <desc>            <address>              <addrLine>New Haven - Connecticut 06520</addrLine>
              <country key="US"></country>
            </address>
          </desc>
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          </listRelation>
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          <desc>            <address>              <addrLine>Yale University School of Medicine, New Haven, Connecticut</addrLine>
              <country key="US"></country>
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          </desc>
        </org>
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</hal:affiliation>
<country>États-Unis</country>
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</author>
</analytic>
<idno type="DOI">10.1117/1.NPh.4.3.031211</idno>
<series><title level="j">Neurophotonics</title>
<idno type="ISSN">2329-423X</idno>
<imprint><date type="datePub">2017-07-01</date>
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<front><div type="abstract" xml:lang="en">              <p>Electrical properties of neuronal processes are extraordinarily complex, dynamic, and, in the general case, impossible to predict in the absence of detailed measurements. To obtain such a measurement one would, ideally, like to be able to monitor electrical subthreshold events as they travel from synapses on distal dendrites and summate at particular locations to initiate action potentials. It is now possible to carry out these measurements at the scale of individual dendritic spines using voltage imaging. In these measurements, the voltage-sensitive probes can be thought of as transmembrane voltmeters with a linear scale, which directly monitor electrical signals. Amiram Grinvald and his colleagues were important early contributors to the methodology of voltage imaging, and they pioneered some of its significant results. In this study, we combined voltage imaging and glutamate uncaging using computer-generated holography (CGH). The results demonstrated that patterned illumination, by reducing the surface area of illuminated membrane, reduces photodynamic damage. Additionally, region-specific illumination practically eliminated the contamination of optical signals from individual spines by the scattered light from the parent dendrite. Finally, patterned illumination allowed one-photon uncaging of glutamate on multiple spines to be carried out in parallel with voltage imaging from the parent dendrite and neighboring spines.</p>
            </div>
</front>
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Imaging membrane potential changes from dendritic spines using computer-generated holography

Imaging membrane potential changes from dendritic spines using computer-generated holography

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