Optical communication with brain cells by means of an implanted duplex micro-device with optogenetics and Ca2+ fluoroimaging
To better understand the brain function based on neural activity, a minimally invasive analysis technology in a freely moving animal is necessary. Such technology would provide new knowledge in neuroscience and contribute to regenerative medical techniques and prosthetics care. An application that c...
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Veröffentlicht in: | Scientific reports 2016-02, Vol.6 (1), p.21247, Article 21247 |
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creator | Kobayashi, Takuma Haruta, Makito Sasagawa, Kiyotaka Matsumata, Miho Eizumi, Kawori Kitsumoto, Chikara Motoyama, Mayumi Maezawa, Yasuyo Ohta, Yasumi Noda, Toshihiko Tokuda, Takashi Ishikawa, Yasuyuki Ohta, Jun |
description | To better understand the brain function based on neural activity, a minimally invasive analysis technology in a freely moving animal is necessary. Such technology would provide new knowledge in neuroscience and contribute to regenerative medical techniques and prosthetics care. An application that combines optogenetics for voluntarily stimulating nerves, imaging to visualize neural activity and a wearable micro-instrument for implantation into the brain could meet the abovementioned demand. To this end, a micro-device that can be applied to the brain less invasively and a system for controlling the device has been newly developed in this study. Since the novel implantable device has dual LEDs and a CMOS image sensor, photostimulation and fluorescence imaging can be performed simultaneously. The device enables bidirectional communication with the brain by means of light. In the present study, the device was evaluated in an
in vitro
experiment using a new on-chip 3D neuroculture with an extracellular matrix gel and an
in vivo
experiment involving regenerative medical transplantation and gene delivery to the brain by using both photosensitive channel and fluorescent Ca
2+
indicator. The device succeeded in activating cells locally by selective photostimulation and the physiological Ca
2+
dynamics of neural cells were visualized simultaneously by fluorescence imaging. |
doi_str_mv | 10.1038/srep21247 |
format | Article |
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in vitro
experiment using a new on-chip 3D neuroculture with an extracellular matrix gel and an
in vivo
experiment involving regenerative medical transplantation and gene delivery to the brain by using both photosensitive channel and fluorescent Ca
2+
indicator. The device succeeded in activating cells locally by selective photostimulation and the physiological Ca
2+
dynamics of neural cells were visualized simultaneously by fluorescence imaging.</description><identifier>ISSN: 2045-2322</identifier><identifier>EISSN: 2045-2322</identifier><identifier>DOI: 10.1038/srep21247</identifier><identifier>PMID: 26878910</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>13 ; 13/106 ; 13/109 ; 14/63 ; 631/1647/2253 ; 639/166/985 ; 64/60 ; Brain ; Calcium imaging ; Calcium signalling ; Extracellular matrix ; Gene transfer ; Genetics ; Humanities and Social Sciences ; Information processing ; multidisciplinary ; Nerves ; Nervous system ; Neuroimaging ; Optics ; Prosthetics ; Science ; Transplantation</subject><ispartof>Scientific reports, 2016-02, Vol.6 (1), p.21247, Article 21247</ispartof><rights>The Author(s) 2016</rights><rights>Copyright Nature Publishing Group Feb 2016</rights><rights>Copyright © 2016, Macmillan Publishers Limited 2016 Macmillan Publishers Limited</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c312t-53e8c6410398ce69d54adf92e46f4c858b69f2654fec37db1cfd9c999aa769e3</citedby><cites>FETCH-LOGICAL-c312t-53e8c6410398ce69d54adf92e46f4c858b69f2654fec37db1cfd9c999aa769e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754641/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754641/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,27924,27925,41120,42189,51576,53791,53793</link.rule.ids></links><search><creatorcontrib>Kobayashi, Takuma</creatorcontrib><creatorcontrib>Haruta, Makito</creatorcontrib><creatorcontrib>Sasagawa, Kiyotaka</creatorcontrib><creatorcontrib>Matsumata, Miho</creatorcontrib><creatorcontrib>Eizumi, Kawori</creatorcontrib><creatorcontrib>Kitsumoto, Chikara</creatorcontrib><creatorcontrib>Motoyama, Mayumi</creatorcontrib><creatorcontrib>Maezawa, Yasuyo</creatorcontrib><creatorcontrib>Ohta, Yasumi</creatorcontrib><creatorcontrib>Noda, Toshihiko</creatorcontrib><creatorcontrib>Tokuda, Takashi</creatorcontrib><creatorcontrib>Ishikawa, Yasuyuki</creatorcontrib><creatorcontrib>Ohta, Jun</creatorcontrib><title>Optical communication with brain cells by means of an implanted duplex micro-device with optogenetics and Ca2+ fluoroimaging</title><title>Scientific reports</title><addtitle>Sci Rep</addtitle><description>To better understand the brain function based on neural activity, a minimally invasive analysis technology in a freely moving animal is necessary. Such technology would provide new knowledge in neuroscience and contribute to regenerative medical techniques and prosthetics care. An application that combines optogenetics for voluntarily stimulating nerves, imaging to visualize neural activity and a wearable micro-instrument for implantation into the brain could meet the abovementioned demand. To this end, a micro-device that can be applied to the brain less invasively and a system for controlling the device has been newly developed in this study. Since the novel implantable device has dual LEDs and a CMOS image sensor, photostimulation and fluorescence imaging can be performed simultaneously. The device enables bidirectional communication with the brain by means of light. In the present study, the device was evaluated in an
in vitro
experiment using a new on-chip 3D neuroculture with an extracellular matrix gel and an
in vivo
experiment involving regenerative medical transplantation and gene delivery to the brain by using both photosensitive channel and fluorescent Ca
2+
indicator. The device succeeded in activating cells locally by selective photostimulation and the physiological Ca
2+
dynamics of neural cells were visualized simultaneously by fluorescence imaging.</description><subject>13</subject><subject>13/106</subject><subject>13/109</subject><subject>14/63</subject><subject>631/1647/2253</subject><subject>639/166/985</subject><subject>64/60</subject><subject>Brain</subject><subject>Calcium imaging</subject><subject>Calcium signalling</subject><subject>Extracellular matrix</subject><subject>Gene transfer</subject><subject>Genetics</subject><subject>Humanities and Social Sciences</subject><subject>Information processing</subject><subject>multidisciplinary</subject><subject>Nerves</subject><subject>Nervous system</subject><subject>Neuroimaging</subject><subject>Optics</subject><subject>Prosthetics</subject><subject>Science</subject><subject>Transplantation</subject><issn>2045-2322</issn><issn>2045-2322</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNplkU1L7TAQhoNcUVEX_oOAK5Vqk6ZtshEuB79AcOM-pMmkRtqkJq3XA_54I0dEudlkYJ555-NF6IiU56Ss-EWKMFFCWbuF9mjJ6oJWlP75Ee-iw5Sey_xqKhgRO2iXNrzlgpR76P1hmp1WA9ZhHBefw9kFj_-5-Ql3UTmPNQxDwt0aj6B8wsFi5bEbp0H5GQw2yzTAGx6djqEw8Oo0bKrDNIcePGT5lEsMXil6hu2whBjcqHrn-wO0bdWQ4PDr30eP11ePq9vi_uHmbvX3vtAVoXNRV8B1w_K2gmtohKmZMlZQYI1lmte8a4SlTc0s6Ko1HdHWCC2EUKptBFT76HIjOy3dCEaDn6Ma5BTzGHEtg3Lyd8a7J9mHV8namuW-WeD4SyCGlwXSLJ_DEn0eWRIuuGjKkrSZOtlQ-RIpu2K_O5BSflolv63K7OmGTZnxPcQfiv_BH5BRlqo</recordid><startdate>20160216</startdate><enddate>20160216</enddate><creator>Kobayashi, Takuma</creator><creator>Haruta, Makito</creator><creator>Sasagawa, Kiyotaka</creator><creator>Matsumata, Miho</creator><creator>Eizumi, Kawori</creator><creator>Kitsumoto, Chikara</creator><creator>Motoyama, Mayumi</creator><creator>Maezawa, Yasuyo</creator><creator>Ohta, Yasumi</creator><creator>Noda, Toshihiko</creator><creator>Tokuda, Takashi</creator><creator>Ishikawa, Yasuyuki</creator><creator>Ohta, Jun</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>5PM</scope></search><sort><creationdate>20160216</creationdate><title>Optical communication with brain cells by means of an implanted duplex micro-device with optogenetics and Ca2+ fluoroimaging</title><author>Kobayashi, Takuma ; 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Such technology would provide new knowledge in neuroscience and contribute to regenerative medical techniques and prosthetics care. An application that combines optogenetics for voluntarily stimulating nerves, imaging to visualize neural activity and a wearable micro-instrument for implantation into the brain could meet the abovementioned demand. To this end, a micro-device that can be applied to the brain less invasively and a system for controlling the device has been newly developed in this study. Since the novel implantable device has dual LEDs and a CMOS image sensor, photostimulation and fluorescence imaging can be performed simultaneously. The device enables bidirectional communication with the brain by means of light. In the present study, the device was evaluated in an
in vitro
experiment using a new on-chip 3D neuroculture with an extracellular matrix gel and an
in vivo
experiment involving regenerative medical transplantation and gene delivery to the brain by using both photosensitive channel and fluorescent Ca
2+
indicator. The device succeeded in activating cells locally by selective photostimulation and the physiological Ca
2+
dynamics of neural cells were visualized simultaneously by fluorescence imaging.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26878910</pmid><doi>10.1038/srep21247</doi><oa>free_for_read</oa></addata></record> |
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subjects | 13 13/106 13/109 14/63 631/1647/2253 639/166/985 64/60 Brain Calcium imaging Calcium signalling Extracellular matrix Gene transfer Genetics Humanities and Social Sciences Information processing multidisciplinary Nerves Nervous system Neuroimaging Optics Prosthetics Science Transplantation |
title | Optical communication with brain cells by means of an implanted duplex micro-device with optogenetics and Ca2+ fluoroimaging |
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