Osteopontin mediates the formation of corpora amylacea-like structures from degenerating neurons in the CA1 region of the rat hippocampus after ischemia
We previously demonstrated that osteopontin (OPN) is closely associated with calcium precipitation in response to ischemic brain insults. The present study was designed to elucidate the possible association between deposition of OPN and progressive neurodegeneration in the ischemic hippocampus. To a...
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Veröffentlicht in: | Cell and tissue research 2022-09, Vol.389 (3), p.443-463 |
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description | We previously demonstrated that osteopontin (OPN) is closely associated with calcium precipitation in response to ischemic brain insults. The present study was designed to elucidate the possible association between deposition of OPN and progressive neurodegeneration in the ischemic hippocampus. To address this, we analyzed the OPN deposits in the rat hippocampus after global cerebral ischemia in the chronic phase (4 to 12 weeks) after reperfusion using immunoelectron microscopy and correlative light and electron microscopy. We identified three different types of OPN deposits based on their morphological characteristics, numbered according to the order in which they evolved. Dark degenerative cells that retained cellular morphology were frequently observed in the pyramidal cell layer, and type I OPN deposits were degenerative mitochondria that accumulated among these cells. Type II deposits evolved into more complex amorphous structures with prominent OPN deposits within their periphery and within degenerative mitochondria-like structures. Finally, type III had large concentric laminated structures with irregularly shaped bodies in the center of the deposits. In all types, OPN expression was closely correlated with calcification, as confirmed by calcium fixation and Alizarin Red staining. Notably, type II and III deposits were highly reminiscent of corpora amylacea, glycoprotein-rich aggregates found in aged brains, or neurodegenerative disease, which was further confirmed by ubiquitin expression and periodic acid-Schiff staining. Overall, our data provide a novel link between ongoing neurodegeneration and the formation of corpora amylacea-like structures and calcium deposits in the ischemic hippocampus, suggesting that OPN may play an important role in such processes. |
doi_str_mv | 10.1007/s00441-022-03645-6 |
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The present study was designed to elucidate the possible association between deposition of OPN and progressive neurodegeneration in the ischemic hippocampus. To address this, we analyzed the OPN deposits in the rat hippocampus after global cerebral ischemia in the chronic phase (4 to 12 weeks) after reperfusion using immunoelectron microscopy and correlative light and electron microscopy. We identified three different types of OPN deposits based on their morphological characteristics, numbered according to the order in which they evolved. Dark degenerative cells that retained cellular morphology were frequently observed in the pyramidal cell layer, and type I OPN deposits were degenerative mitochondria that accumulated among these cells. Type II deposits evolved into more complex amorphous structures with prominent OPN deposits within their periphery and within degenerative mitochondria-like structures. Finally, type III had large concentric laminated structures with irregularly shaped bodies in the center of the deposits. In all types, OPN expression was closely correlated with calcification, as confirmed by calcium fixation and Alizarin Red staining. Notably, type II and III deposits were highly reminiscent of corpora amylacea, glycoprotein-rich aggregates found in aged brains, or neurodegenerative disease, which was further confirmed by ubiquitin expression and periodic acid-Schiff staining. Overall, our data provide a novel link between ongoing neurodegeneration and the formation of corpora amylacea-like structures and calcium deposits in the ischemic hippocampus, suggesting that OPN may play an important role in such processes.</description><identifier>ISSN: 0302-766X</identifier><identifier>EISSN: 1432-0878</identifier><identifier>DOI: 10.1007/s00441-022-03645-6</identifier><identifier>PMID: 35688947</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Brain ; Brain injury ; Calcification ; Calcium ; Cytology ; Deposits ; Electron microscopy ; Hippocampus ; Human Genetics ; Immunoelectron microscopy ; Ischemia ; Microscopy ; Mitochondria ; Molecular Medicine ; Nervous system diseases ; Neurodegeneration ; Neurodegenerative diseases ; Neurons ; Osteopontin ; Physical characteristics ; Proteomics ; Regular Article ; Reperfusion ; Ubiquitin</subject><ispartof>Cell and tissue research, 2022-09, Vol.389 (3), p.443-463</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022</rights><rights>2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.</rights><rights>COPYRIGHT 2022 Springer</rights><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature 2022.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c473t-49635728b2d71454cd262499d70184423a0c9194ce66435dc2e8ade7b023bb533</citedby><cites>FETCH-LOGICAL-c473t-49635728b2d71454cd262499d70184423a0c9194ce66435dc2e8ade7b023bb533</cites><orcidid>0000-0002-9660-8584</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00441-022-03645-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00441-022-03645-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35688947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Riew, Tae-Ryong</creatorcontrib><creatorcontrib>Jin, Xuyan</creatorcontrib><creatorcontrib>Hwang, Ji-Won</creatorcontrib><creatorcontrib>Kim, Soojin</creatorcontrib><creatorcontrib>Kim, Hong Lim</creatorcontrib><creatorcontrib>Lee, Mun-Yong</creatorcontrib><title>Osteopontin mediates the formation of corpora amylacea-like structures from degenerating neurons in the CA1 region of the rat hippocampus after ischemia</title><title>Cell and tissue research</title><addtitle>Cell Tissue Res</addtitle><addtitle>Cell Tissue Res</addtitle><description>We previously demonstrated that osteopontin (OPN) is closely associated with calcium precipitation in response to ischemic brain insults. The present study was designed to elucidate the possible association between deposition of OPN and progressive neurodegeneration in the ischemic hippocampus. To address this, we analyzed the OPN deposits in the rat hippocampus after global cerebral ischemia in the chronic phase (4 to 12 weeks) after reperfusion using immunoelectron microscopy and correlative light and electron microscopy. We identified three different types of OPN deposits based on their morphological characteristics, numbered according to the order in which they evolved. Dark degenerative cells that retained cellular morphology were frequently observed in the pyramidal cell layer, and type I OPN deposits were degenerative mitochondria that accumulated among these cells. Type II deposits evolved into more complex amorphous structures with prominent OPN deposits within their periphery and within degenerative mitochondria-like structures. Finally, type III had large concentric laminated structures with irregularly shaped bodies in the center of the deposits. In all types, OPN expression was closely correlated with calcification, as confirmed by calcium fixation and Alizarin Red staining. Notably, type II and III deposits were highly reminiscent of corpora amylacea, glycoprotein-rich aggregates found in aged brains, or neurodegenerative disease, which was further confirmed by ubiquitin expression and periodic acid-Schiff staining. Overall, our data provide a novel link between ongoing neurodegeneration and the formation of corpora amylacea-like structures and calcium deposits in the ischemic hippocampus, suggesting that OPN may play an important role in such processes.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain</subject><subject>Brain injury</subject><subject>Calcification</subject><subject>Calcium</subject><subject>Cytology</subject><subject>Deposits</subject><subject>Electron microscopy</subject><subject>Hippocampus</subject><subject>Human Genetics</subject><subject>Immunoelectron microscopy</subject><subject>Ischemia</subject><subject>Microscopy</subject><subject>Mitochondria</subject><subject>Molecular Medicine</subject><subject>Nervous system diseases</subject><subject>Neurodegeneration</subject><subject>Neurodegenerative diseases</subject><subject>Neurons</subject><subject>Osteopontin</subject><subject>Physical characteristics</subject><subject>Proteomics</subject><subject>Regular Article</subject><subject>Reperfusion</subject><subject>Ubiquitin</subject><issn>0302-766X</issn><issn>1432-0878</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kk2L1TAUhosoznX0D7iQgCBuOuarSbO8XJxRGJiNgruQpqcfY5vUJF3MP_HnmnqvjiMiWYScPO_LOZy3KF4SfEEwlu8ixpyTElNaYiZ4VYpHxY5wlp-1rB8XO8wwLaUQX86KZzHeYky4EOppccYqUdeKy13x_SYm8It3aXRohnY0CSJKA6DOh9mk0TvkO2R9WHwwyMx3k7Fgymn8CiimsNq0hqzogp9RCz04CFnleuRgDd5FlH03u8OeoAD9yW-rZA4N47J4a-Zljch0CQIaox1gHs3z4klnpggvTvd58fny_afDh_L65urjYX9dWi5ZKrkSrJK0bmgrCa-4bamgXKlWYlJzTpnBVhHFLQjBWdVaCrVpQTaYsqapGDsv3h59l-C_rRCTnnMLME3GgV-jpkJWAhOsZEZf_4Xe-jW43J2mEte1pFiIe6o3E-jRdT4FYzdTvZekUpQxxTN18Q8qnzYPb72Dbsz1B4I3fwgGMFMaop_WbUPxIUiPoA0-xgCdXsI4m3CnCdZbbvQxNzrnRv_Mjd6afnUabW1yCn5LfgUlA-wIxPzlegj3s__H9gc9WMy5</recordid><startdate>20220901</startdate><enddate>20220901</enddate><creator>Riew, Tae-Ryong</creator><creator>Jin, Xuyan</creator><creator>Hwang, Ji-Won</creator><creator>Kim, Soojin</creator><creator>Kim, Hong Lim</creator><creator>Lee, Mun-Yong</creator><general>Springer Berlin Heidelberg</general><general>Springer</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7QR</scope><scope>7RV</scope><scope>7SS</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</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>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9660-8584</orcidid></search><sort><creationdate>20220901</creationdate><title>Osteopontin mediates the formation of corpora amylacea-like structures from degenerating neurons in the CA1 region of the rat hippocampus after ischemia</title><author>Riew, Tae-Ryong ; 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The present study was designed to elucidate the possible association between deposition of OPN and progressive neurodegeneration in the ischemic hippocampus. To address this, we analyzed the OPN deposits in the rat hippocampus after global cerebral ischemia in the chronic phase (4 to 12 weeks) after reperfusion using immunoelectron microscopy and correlative light and electron microscopy. We identified three different types of OPN deposits based on their morphological characteristics, numbered according to the order in which they evolved. Dark degenerative cells that retained cellular morphology were frequently observed in the pyramidal cell layer, and type I OPN deposits were degenerative mitochondria that accumulated among these cells. Type II deposits evolved into more complex amorphous structures with prominent OPN deposits within their periphery and within degenerative mitochondria-like structures. Finally, type III had large concentric laminated structures with irregularly shaped bodies in the center of the deposits. In all types, OPN expression was closely correlated with calcification, as confirmed by calcium fixation and Alizarin Red staining. Notably, type II and III deposits were highly reminiscent of corpora amylacea, glycoprotein-rich aggregates found in aged brains, or neurodegenerative disease, which was further confirmed by ubiquitin expression and periodic acid-Schiff staining. Overall, our data provide a novel link between ongoing neurodegeneration and the formation of corpora amylacea-like structures and calcium deposits in the ischemic hippocampus, suggesting that OPN may play an important role in such processes.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>35688947</pmid><doi>10.1007/s00441-022-03645-6</doi><tpages>21</tpages><orcidid>https://orcid.org/0000-0002-9660-8584</orcidid></addata></record> |
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subjects | Biomedical and Life Sciences Biomedicine Brain Brain injury Calcification Calcium Cytology Deposits Electron microscopy Hippocampus Human Genetics Immunoelectron microscopy Ischemia Microscopy Mitochondria Molecular Medicine Nervous system diseases Neurodegeneration Neurodegenerative diseases Neurons Osteopontin Physical characteristics Proteomics Regular Article Reperfusion Ubiquitin |
title | Osteopontin mediates the formation of corpora amylacea-like structures from degenerating neurons in the CA1 region of the rat hippocampus after ischemia |
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