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Retina-to-brain spreading of α-synuclein after intravitreal injection of preformed fibrils
Parkinson's disease (PD) is a neurodegenerative disorder characterized by the aggregation of misfolded α-synuclein and progressive spreading of the aggregates from a few discrete regions to wider brain regions. Although PD has been classically considered a movement disorder, a large body of cli...
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Published in: | Acta neuropathologica communications 2023-05, Vol.11 (1), p.83-20, Article 83 |
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description | Parkinson's disease (PD) is a neurodegenerative disorder characterized by the aggregation of misfolded α-synuclein and progressive spreading of the aggregates from a few discrete regions to wider brain regions. Although PD has been classically considered a movement disorder, a large body of clinical evidence has revealed the progressive occurrence of non-motor symptoms. Patients present visual symptoms in the initial stages of the disease, and accumulation of phospho-α-synuclein, dopaminergic neuronal loss, and retinal thinning has been observed in the retinas of PD patients. Based on such human data, we hypothesized that α-synuclein aggregation can initiate in the retina and spread to the brain through the visual pathway. Here, we demonstrate accumulation of α-synuclein in the retinas and brains of naive mice after intravitreal injection of α-synuclein preformed fibrils (PFFs). Histological analyses showed deposition of phospho-α-synuclein inclusions within the retina 2 months after injection, with increased oxidative stress leading to loss of retinal ganglion cells and dopaminergic dysfunction. In addition, we found accumulation of phospho-α-synuclein in cortical areas with accompanying neuroinflammation after 5 months. Collectively, our findings suggest that retinal synucleinopathy lesions initiated by intravitreal injection of α-synuclein PFFs spread to various brain regions through the visual pathway in mice. |
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Although PD has been classically considered a movement disorder, a large body of clinical evidence has revealed the progressive occurrence of non-motor symptoms. Patients present visual symptoms in the initial stages of the disease, and accumulation of phospho-α-synuclein, dopaminergic neuronal loss, and retinal thinning has been observed in the retinas of PD patients. Based on such human data, we hypothesized that α-synuclein aggregation can initiate in the retina and spread to the brain through the visual pathway. Here, we demonstrate accumulation of α-synuclein in the retinas and brains of naive mice after intravitreal injection of α-synuclein preformed fibrils (PFFs). Histological analyses showed deposition of phospho-α-synuclein inclusions within the retina 2 months after injection, with increased oxidative stress leading to loss of retinal ganglion cells and dopaminergic dysfunction. In addition, we found accumulation of phospho-α-synuclein in cortical areas with accompanying neuroinflammation after 5 months. Collectively, our findings suggest that retinal synucleinopathy lesions initiated by intravitreal injection of α-synuclein PFFs spread to various brain regions through the visual pathway in mice.</description><identifier>ISSN: 2051-5960</identifier><identifier>EISSN: 2051-5960</identifier><identifier>DOI: 10.1186/s40478-023-01575-0</identifier><identifier>PMID: 37210559</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>alpha-Synuclein - metabolism ; Animals ; Antigens ; Brain ; Brain - pathology ; Chromatography ; Cloning ; Graph representations ; Humans ; Hypotheses ; Intravitreal Injections ; Laboratories ; Mice ; Microscopy ; Parkinson Disease - pathology ; Parkinson's disease ; Pathology ; Protein aggregation ; Proteins ; Retina ; Retina - pathology ; Retinal degeneration ; Spectrum analysis ; α-synuclein</subject><ispartof>Acta neuropathologica communications, 2023-05, Vol.11 (1), p.83-20, Article 83</ispartof><rights>2023. The Author(s).</rights><rights>2023. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4120-5e0e3b23e300cd4a1967aeae30e7a0475d8018e19887250c054a70a05f26cc4c3</citedby><cites>FETCH-LOGICAL-c4120-5e0e3b23e300cd4a1967aeae30e7a0475d8018e19887250c054a70a05f26cc4c3</cites><orcidid>0000-0002-5155-5335</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10199563/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2827115063?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37210559$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pérez-Acuña, Dayana</creatorcontrib><creatorcontrib>Rhee, Ka Hyun</creatorcontrib><creatorcontrib>Shin, Soo Jean</creatorcontrib><creatorcontrib>Ahn, Jeeyun</creatorcontrib><creatorcontrib>Lee, Jee-Young</creatorcontrib><creatorcontrib>Lee, Seung-Jae</creatorcontrib><title>Retina-to-brain spreading of α-synuclein after intravitreal injection of preformed fibrils</title><title>Acta neuropathologica communications</title><addtitle>Acta Neuropathol Commun</addtitle><description>Parkinson's disease (PD) is a neurodegenerative disorder characterized by the aggregation of misfolded α-synuclein and progressive spreading of the aggregates from a few discrete regions to wider brain regions. Although PD has been classically considered a movement disorder, a large body of clinical evidence has revealed the progressive occurrence of non-motor symptoms. Patients present visual symptoms in the initial stages of the disease, and accumulation of phospho-α-synuclein, dopaminergic neuronal loss, and retinal thinning has been observed in the retinas of PD patients. Based on such human data, we hypothesized that α-synuclein aggregation can initiate in the retina and spread to the brain through the visual pathway. Here, we demonstrate accumulation of α-synuclein in the retinas and brains of naive mice after intravitreal injection of α-synuclein preformed fibrils (PFFs). Histological analyses showed deposition of phospho-α-synuclein inclusions within the retina 2 months after injection, with increased oxidative stress leading to loss of retinal ganglion cells and dopaminergic dysfunction. In addition, we found accumulation of phospho-α-synuclein in cortical areas with accompanying neuroinflammation after 5 months. Collectively, our findings suggest that retinal synucleinopathy lesions initiated by intravitreal injection of α-synuclein PFFs spread to various brain regions through the visual pathway in mice.</description><subject>alpha-Synuclein - metabolism</subject><subject>Animals</subject><subject>Antigens</subject><subject>Brain</subject><subject>Brain - pathology</subject><subject>Chromatography</subject><subject>Cloning</subject><subject>Graph representations</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Intravitreal Injections</subject><subject>Laboratories</subject><subject>Mice</subject><subject>Microscopy</subject><subject>Parkinson Disease - pathology</subject><subject>Parkinson's disease</subject><subject>Pathology</subject><subject>Protein aggregation</subject><subject>Proteins</subject><subject>Retina</subject><subject>Retina - pathology</subject><subject>Retinal degeneration</subject><subject>Spectrum analysis</subject><subject>α-synuclein</subject><issn>2051-5960</issn><issn>2051-5960</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdks9u1DAQxi0EolXpC3BAkbhwMcz4T2yfEKoKVKqEVLUnDpbjOItX2Xixk0p9LF6EZ8K7W6q2vtjj-eYnf-Mh5C3CR0TdfioChNIUGKeAUkkKL8gxA4lUmhZePjofkdNS1lCXQeRavyZHXDEEKc0x-XkV5jg5OifaZRenpmxzcH2cVk0amr9_aLmbFj-GmnHDHHITpzm72zhX1ViDdfBzTNNOXAuHlDehb4bY5TiWN-TV4MYSTu_3E3Lz9fz67Du9_PHt4uzLJfUCGVAZIPCO8cABfC8cmla54GoYlKsmZa8BdUCjtWISPEjhFDiQA2u9F56fkIsDt09ubbc5bly-s8lFu79IeWVdnmN1YYVjSplBeMVAtNybMHjNeN97I7oWoLI-H1jbpatWfNjZHZ9An2am-Muu0q1FQGNkyyvhwz0hp99LKLPdxOLDOLoppKVYprFV0kglqvT9M-k6LXmqvaoqphAl7IHsoPI5lVKb_PAaBLubBXuYBVtnwe5nwe58vHvs46Hk_8_zfwnVr6Y</recordid><startdate>20230520</startdate><enddate>20230520</enddate><creator>Pérez-Acuña, Dayana</creator><creator>Rhee, Ka Hyun</creator><creator>Shin, Soo Jean</creator><creator>Ahn, Jeeyun</creator><creator>Lee, Jee-Young</creator><creator>Lee, Seung-Jae</creator><general>BioMed Central</general><general>BMC</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-5155-5335</orcidid></search><sort><creationdate>20230520</creationdate><title>Retina-to-brain spreading of α-synuclein after intravitreal injection of preformed fibrils</title><author>Pérez-Acuña, Dayana ; Rhee, Ka Hyun ; Shin, Soo Jean ; Ahn, Jeeyun ; Lee, Jee-Young ; Lee, Seung-Jae</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4120-5e0e3b23e300cd4a1967aeae30e7a0475d8018e19887250c054a70a05f26cc4c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>alpha-Synuclein - metabolism</topic><topic>Animals</topic><topic>Antigens</topic><topic>Brain</topic><topic>Brain - pathology</topic><topic>Chromatography</topic><topic>Cloning</topic><topic>Graph representations</topic><topic>Humans</topic><topic>Hypotheses</topic><topic>Intravitreal Injections</topic><topic>Laboratories</topic><topic>Mice</topic><topic>Microscopy</topic><topic>Parkinson Disease - pathology</topic><topic>Parkinson's disease</topic><topic>Pathology</topic><topic>Protein aggregation</topic><topic>Proteins</topic><topic>Retina</topic><topic>Retina - pathology</topic><topic>Retinal degeneration</topic><topic>Spectrum analysis</topic><topic>α-synuclein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pérez-Acuña, Dayana</creatorcontrib><creatorcontrib>Rhee, Ka Hyun</creatorcontrib><creatorcontrib>Shin, Soo Jean</creatorcontrib><creatorcontrib>Ahn, Jeeyun</creatorcontrib><creatorcontrib>Lee, Jee-Young</creatorcontrib><creatorcontrib>Lee, Seung-Jae</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Acta neuropathologica communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pérez-Acuña, Dayana</au><au>Rhee, Ka Hyun</au><au>Shin, Soo Jean</au><au>Ahn, Jeeyun</au><au>Lee, Jee-Young</au><au>Lee, Seung-Jae</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Retina-to-brain spreading of α-synuclein after intravitreal injection of preformed fibrils</atitle><jtitle>Acta neuropathologica communications</jtitle><addtitle>Acta Neuropathol Commun</addtitle><date>2023-05-20</date><risdate>2023</risdate><volume>11</volume><issue>1</issue><spage>83</spage><epage>20</epage><pages>83-20</pages><artnum>83</artnum><issn>2051-5960</issn><eissn>2051-5960</eissn><abstract>Parkinson's disease (PD) is a neurodegenerative disorder characterized by the aggregation of misfolded α-synuclein and progressive spreading of the aggregates from a few discrete regions to wider brain regions. Although PD has been classically considered a movement disorder, a large body of clinical evidence has revealed the progressive occurrence of non-motor symptoms. Patients present visual symptoms in the initial stages of the disease, and accumulation of phospho-α-synuclein, dopaminergic neuronal loss, and retinal thinning has been observed in the retinas of PD patients. Based on such human data, we hypothesized that α-synuclein aggregation can initiate in the retina and spread to the brain through the visual pathway. Here, we demonstrate accumulation of α-synuclein in the retinas and brains of naive mice after intravitreal injection of α-synuclein preformed fibrils (PFFs). Histological analyses showed deposition of phospho-α-synuclein inclusions within the retina 2 months after injection, with increased oxidative stress leading to loss of retinal ganglion cells and dopaminergic dysfunction. In addition, we found accumulation of phospho-α-synuclein in cortical areas with accompanying neuroinflammation after 5 months. Collectively, our findings suggest that retinal synucleinopathy lesions initiated by intravitreal injection of α-synuclein PFFs spread to various brain regions through the visual pathway in mice.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>37210559</pmid><doi>10.1186/s40478-023-01575-0</doi><tpages>20</tpages><orcidid>https://orcid.org/0000-0002-5155-5335</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | alpha-Synuclein - metabolism Animals Antigens Brain Brain - pathology Chromatography Cloning Graph representations Humans Hypotheses Intravitreal Injections Laboratories Mice Microscopy Parkinson Disease - pathology Parkinson's disease Pathology Protein aggregation Proteins Retina Retina - pathology Retinal degeneration Spectrum analysis α-synuclein |
title | Retina-to-brain spreading of α-synuclein after intravitreal injection of preformed fibrils |
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