Sonogenetic-Based Neuromodulation for the Amelioration of Parkinson’s Disease
Sonogenetics is a promising strategy allowing the noninvasive and selective activation of targeted neurons in deep brain regions; nevertheless, its therapeutic outcome for neurodegeneration diseases that need long-term treatment remains to be verified. We previously enhanced the ultrasound (US) sens...
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Veröffentlicht in: | Nano letters 2021-07, Vol.21 (14), p.5967-5976 |
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creator | Fan, Ching-Hsiang Wei, Kuo-Chen Chiu, Nai-Hua Liao, En-Chi Wang, Hsien-Chu Wu, Ruo-Yu Ho, Yi-Ju Chan, Hong-Lin Wang, Tsung-Shing Andrew Huang, Ying-Zu Hsieh, Tsung-Hsun Lin, Chin-Hsien Lin, Yu-Chun Yeh, Chih-Kuang |
description | Sonogenetics is a promising strategy allowing the noninvasive and selective activation of targeted neurons in deep brain regions; nevertheless, its therapeutic outcome for neurodegeneration diseases that need long-term treatment remains to be verified. We previously enhanced the ultrasound (US) sensitivity of targeted cells by genetic modification with an engineered auditory-sensing protein, mPrestin (N7T, N308S). In this study, we expressed mPrestin in the dopaminergic neurons of the substantia nigra in Parkinson’s disease (PD) mice and used 0.5 MHz US for repeated and localized brain stimulation. The mPrestin expression in dopaminergic neurons persisted for at least 56 days after a single shot of adeno-associated virus, suggesting that the period of expression was long enough for US treatment in mice. Compared to untreated mice, US stimulation ameliorated the dopaminergic neurodegeneration 10-fold and mitigated the PD symptoms of the mice 4-fold, suggesting that this sonogenetic strategy has the clinical potential to treat neurodegenerative diseases. |
doi_str_mv | 10.1021/acs.nanolett.1c00886 |
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We previously enhanced the ultrasound (US) sensitivity of targeted cells by genetic modification with an engineered auditory-sensing protein, mPrestin (N7T, N308S). In this study, we expressed mPrestin in the dopaminergic neurons of the substantia nigra in Parkinson’s disease (PD) mice and used 0.5 MHz US for repeated and localized brain stimulation. The mPrestin expression in dopaminergic neurons persisted for at least 56 days after a single shot of adeno-associated virus, suggesting that the period of expression was long enough for US treatment in mice. Compared to untreated mice, US stimulation ameliorated the dopaminergic neurodegeneration 10-fold and mitigated the PD symptoms of the mice 4-fold, suggesting that this sonogenetic strategy has the clinical potential to treat neurodegenerative diseases.</description><identifier>ISSN: 1530-6984</identifier><identifier>EISSN: 1530-6992</identifier><identifier>DOI: 10.1021/acs.nanolett.1c00886</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Nano letters, 2021-07, Vol.21 (14), p.5967-5976</ispartof><rights>2021 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a325t-22443535858f38d9dbeb1eaa0c9f7890b0f4722f8253e6706a84a52652a138793</citedby><cites>FETCH-LOGICAL-a325t-22443535858f38d9dbeb1eaa0c9f7890b0f4722f8253e6706a84a52652a138793</cites><orcidid>0000-0002-9629-7560 ; 0000-0002-2880-6327</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.nanolett.1c00886$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.nanolett.1c00886$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids></links><search><creatorcontrib>Fan, Ching-Hsiang</creatorcontrib><creatorcontrib>Wei, Kuo-Chen</creatorcontrib><creatorcontrib>Chiu, Nai-Hua</creatorcontrib><creatorcontrib>Liao, En-Chi</creatorcontrib><creatorcontrib>Wang, Hsien-Chu</creatorcontrib><creatorcontrib>Wu, Ruo-Yu</creatorcontrib><creatorcontrib>Ho, Yi-Ju</creatorcontrib><creatorcontrib>Chan, Hong-Lin</creatorcontrib><creatorcontrib>Wang, Tsung-Shing Andrew</creatorcontrib><creatorcontrib>Huang, Ying-Zu</creatorcontrib><creatorcontrib>Hsieh, Tsung-Hsun</creatorcontrib><creatorcontrib>Lin, Chin-Hsien</creatorcontrib><creatorcontrib>Lin, Yu-Chun</creatorcontrib><creatorcontrib>Yeh, Chih-Kuang</creatorcontrib><title>Sonogenetic-Based Neuromodulation for the Amelioration of Parkinson’s Disease</title><title>Nano letters</title><addtitle>Nano Lett</addtitle><description>Sonogenetics is a promising strategy allowing the noninvasive and selective activation of targeted neurons in deep brain regions; nevertheless, its therapeutic outcome for neurodegeneration diseases that need long-term treatment remains to be verified. We previously enhanced the ultrasound (US) sensitivity of targeted cells by genetic modification with an engineered auditory-sensing protein, mPrestin (N7T, N308S). In this study, we expressed mPrestin in the dopaminergic neurons of the substantia nigra in Parkinson’s disease (PD) mice and used 0.5 MHz US for repeated and localized brain stimulation. The mPrestin expression in dopaminergic neurons persisted for at least 56 days after a single shot of adeno-associated virus, suggesting that the period of expression was long enough for US treatment in mice. Compared to untreated mice, US stimulation ameliorated the dopaminergic neurodegeneration 10-fold and mitigated the PD symptoms of the mice 4-fold, suggesting that this sonogenetic strategy has the clinical potential to treat neurodegenerative diseases.</description><issn>1530-6984</issn><issn>1530-6992</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp9kL9OwzAQhy0EEqXwBgwZWVLOdpw4Yyl_pYoiAbPlJGdISexiJwMbr8Hr8SSkSmFkutPd7zvpPkJOKcwoMHquyzCz2roGu25GSwAp0z0yoYJDnOY52__rZXJIjkJYA0DOBUzI6tFZ94IWu7qML3TAKrrH3rvWVX2ju9rZyDgfda8YzVtsaufHoTPRg_ZvtQ3Ofn9-heiyDjjgx-TA6Cbgya5OyfP11dPiNl6ubu4W82WsORNdzFiScMGFFNJwWeVVgQVFraHMTSZzKMAkGWNGMsExzSDVMtGCpYJpymWW8yk5G-9uvHvvMXSqrUOJTaMtuj4oJgQDIVIGQzQZo6V3IXg0auPrVvsPRUFt_anBn_r1p3b-BgxGbLtdu97b4Z__kR_mY3hr</recordid><startdate>20210728</startdate><enddate>20210728</enddate><creator>Fan, Ching-Hsiang</creator><creator>Wei, Kuo-Chen</creator><creator>Chiu, Nai-Hua</creator><creator>Liao, En-Chi</creator><creator>Wang, Hsien-Chu</creator><creator>Wu, Ruo-Yu</creator><creator>Ho, Yi-Ju</creator><creator>Chan, Hong-Lin</creator><creator>Wang, Tsung-Shing Andrew</creator><creator>Huang, Ying-Zu</creator><creator>Hsieh, Tsung-Hsun</creator><creator>Lin, Chin-Hsien</creator><creator>Lin, Yu-Chun</creator><creator>Yeh, Chih-Kuang</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9629-7560</orcidid><orcidid>https://orcid.org/0000-0002-2880-6327</orcidid></search><sort><creationdate>20210728</creationdate><title>Sonogenetic-Based Neuromodulation for the Amelioration of Parkinson’s Disease</title><author>Fan, Ching-Hsiang ; Wei, Kuo-Chen ; Chiu, Nai-Hua ; Liao, En-Chi ; Wang, Hsien-Chu ; Wu, Ruo-Yu ; Ho, Yi-Ju ; Chan, Hong-Lin ; Wang, Tsung-Shing Andrew ; Huang, Ying-Zu ; Hsieh, Tsung-Hsun ; Lin, Chin-Hsien ; Lin, Yu-Chun ; Yeh, Chih-Kuang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a325t-22443535858f38d9dbeb1eaa0c9f7890b0f4722f8253e6706a84a52652a138793</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fan, Ching-Hsiang</creatorcontrib><creatorcontrib>Wei, Kuo-Chen</creatorcontrib><creatorcontrib>Chiu, Nai-Hua</creatorcontrib><creatorcontrib>Liao, En-Chi</creatorcontrib><creatorcontrib>Wang, Hsien-Chu</creatorcontrib><creatorcontrib>Wu, Ruo-Yu</creatorcontrib><creatorcontrib>Ho, Yi-Ju</creatorcontrib><creatorcontrib>Chan, Hong-Lin</creatorcontrib><creatorcontrib>Wang, Tsung-Shing Andrew</creatorcontrib><creatorcontrib>Huang, Ying-Zu</creatorcontrib><creatorcontrib>Hsieh, Tsung-Hsun</creatorcontrib><creatorcontrib>Lin, Chin-Hsien</creatorcontrib><creatorcontrib>Lin, Yu-Chun</creatorcontrib><creatorcontrib>Yeh, Chih-Kuang</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Nano letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fan, Ching-Hsiang</au><au>Wei, Kuo-Chen</au><au>Chiu, Nai-Hua</au><au>Liao, En-Chi</au><au>Wang, Hsien-Chu</au><au>Wu, Ruo-Yu</au><au>Ho, Yi-Ju</au><au>Chan, Hong-Lin</au><au>Wang, Tsung-Shing Andrew</au><au>Huang, Ying-Zu</au><au>Hsieh, Tsung-Hsun</au><au>Lin, Chin-Hsien</au><au>Lin, Yu-Chun</au><au>Yeh, Chih-Kuang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sonogenetic-Based Neuromodulation for the Amelioration of Parkinson’s Disease</atitle><jtitle>Nano letters</jtitle><addtitle>Nano Lett</addtitle><date>2021-07-28</date><risdate>2021</risdate><volume>21</volume><issue>14</issue><spage>5967</spage><epage>5976</epage><pages>5967-5976</pages><issn>1530-6984</issn><eissn>1530-6992</eissn><abstract>Sonogenetics is a promising strategy allowing the noninvasive and selective activation of targeted neurons in deep brain regions; nevertheless, its therapeutic outcome for neurodegeneration diseases that need long-term treatment remains to be verified. We previously enhanced the ultrasound (US) sensitivity of targeted cells by genetic modification with an engineered auditory-sensing protein, mPrestin (N7T, N308S). In this study, we expressed mPrestin in the dopaminergic neurons of the substantia nigra in Parkinson’s disease (PD) mice and used 0.5 MHz US for repeated and localized brain stimulation. The mPrestin expression in dopaminergic neurons persisted for at least 56 days after a single shot of adeno-associated virus, suggesting that the period of expression was long enough for US treatment in mice. Compared to untreated mice, US stimulation ameliorated the dopaminergic neurodegeneration 10-fold and mitigated the PD symptoms of the mice 4-fold, suggesting that this sonogenetic strategy has the clinical potential to treat neurodegenerative diseases.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.nanolett.1c00886</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-9629-7560</orcidid><orcidid>https://orcid.org/0000-0002-2880-6327</orcidid></addata></record> |
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title | Sonogenetic-Based Neuromodulation for the Amelioration of Parkinson’s Disease |
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