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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Cell and tissue research 2022-09, Vol.389 (3), p.443-463
Hauptverfasser: Riew, Tae-Ryong, Jin, Xuyan, Hwang, Ji-Won, Kim, Soojin, Kim, Hong Lim, Lee, Mun-Yong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 463
container_issue 3
container_start_page 443
container_title Cell and tissue research
container_volume 389
creator Riew, Tae-Ryong
Jin, Xuyan
Hwang, Ji-Won
Kim, Soojin
Kim, Hong Lim
Lee, Mun-Yong
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
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2675601097</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A715923394</galeid><sourcerecordid>A715923394</sourcerecordid><originalsourceid>FETCH-LOGICAL-c473t-49635728b2d71454cd262499d70184423a0c9194ce66435dc2e8ade7b023bb533</originalsourceid><addsrcrecordid>eNp9kk2L1TAUhosoznX0D7iQgCBuOuarSbO8XJxRGJiNgruQpqcfY5vUJF3MP_HnmnqvjiMiWYScPO_LOZy3KF4SfEEwlu8ixpyTElNaYiZ4VYpHxY5wlp-1rB8XO8wwLaUQX86KZzHeYky4EOppccYqUdeKy13x_SYm8It3aXRohnY0CSJKA6DOh9mk0TvkO2R9WHwwyMx3k7Fgymn8CiimsNq0hqzogp9RCz04CFnleuRgDd5FlH03u8OeoAD9yW-rZA4N47J4a-Zljch0CQIaox1gHs3z4klnpggvTvd58fny_afDh_L65urjYX9dWi5ZKrkSrJK0bmgrCa-4bamgXKlWYlJzTpnBVhHFLQjBWdVaCrVpQTaYsqapGDsv3h59l-C_rRCTnnMLME3GgV-jpkJWAhOsZEZf_4Xe-jW43J2mEte1pFiIe6o3E-jRdT4FYzdTvZekUpQxxTN18Q8qnzYPb72Dbsz1B4I3fwgGMFMaop_WbUPxIUiPoA0-xgCdXsI4m3CnCdZbbvQxNzrnRv_Mjd6afnUabW1yCn5LfgUlA-wIxPzlegj3s__H9gc9WMy5</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2708872066</pqid></control><display><type>article</type><title>Osteopontin mediates the formation of corpora amylacea-like structures from degenerating neurons in the CA1 region of the rat hippocampus after ischemia</title><source>SpringerLink Journals - AutoHoldings</source><creator>Riew, Tae-Ryong ; Jin, Xuyan ; Hwang, Ji-Won ; Kim, Soojin ; Kim, Hong Lim ; Lee, Mun-Yong</creator><creatorcontrib>Riew, Tae-Ryong ; Jin, Xuyan ; Hwang, Ji-Won ; Kim, Soojin ; Kim, Hong Lim ; Lee, Mun-Yong</creatorcontrib><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><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 ; Jin, Xuyan ; Hwang, Ji-Won ; Kim, Soojin ; Kim, Hong Lim ; Lee, Mun-Yong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c473t-49635728b2d71454cd262499d70184423a0c9194ce66435dc2e8ade7b023bb533</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain</topic><topic>Brain injury</topic><topic>Calcification</topic><topic>Calcium</topic><topic>Cytology</topic><topic>Deposits</topic><topic>Electron microscopy</topic><topic>Hippocampus</topic><topic>Human Genetics</topic><topic>Immunoelectron microscopy</topic><topic>Ischemia</topic><topic>Microscopy</topic><topic>Mitochondria</topic><topic>Molecular Medicine</topic><topic>Nervous system diseases</topic><topic>Neurodegeneration</topic><topic>Neurodegenerative diseases</topic><topic>Neurons</topic><topic>Osteopontin</topic><topic>Physical characteristics</topic><topic>Proteomics</topic><topic>Regular Article</topic><topic>Reperfusion</topic><topic>Ubiquitin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Nursing &amp; Allied Health Database</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Neurosciences Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</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>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cell and tissue research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Riew, Tae-Ryong</au><au>Jin, Xuyan</au><au>Hwang, Ji-Won</au><au>Kim, Soojin</au><au>Kim, Hong Lim</au><au>Lee, Mun-Yong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Osteopontin mediates the formation of corpora amylacea-like structures from degenerating neurons in the CA1 region of the rat hippocampus after ischemia</atitle><jtitle>Cell and tissue research</jtitle><stitle>Cell Tissue Res</stitle><addtitle>Cell Tissue Res</addtitle><date>2022-09-01</date><risdate>2022</risdate><volume>389</volume><issue>3</issue><spage>443</spage><epage>463</epage><pages>443-463</pages><issn>0302-766X</issn><eissn>1432-0878</eissn><abstract>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.</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>
fulltext fulltext
identifier ISSN: 0302-766X
ispartof Cell and tissue research, 2022-09, Vol.389 (3), p.443-463
issn 0302-766X
1432-0878
language eng
recordid cdi_proquest_miscellaneous_2675601097
source SpringerLink Journals - AutoHoldings
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T05%3A30%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Osteopontin%20mediates%20the%20formation%20of%20corpora%20amylacea-like%20structures%20from%20degenerating%20neurons%20in%20the%20CA1%20region%20of%20the%20rat%20hippocampus%20after%20ischemia&rft.jtitle=Cell%20and%20tissue%20research&rft.au=Riew,%20Tae-Ryong&rft.date=2022-09-01&rft.volume=389&rft.issue=3&rft.spage=443&rft.epage=463&rft.pages=443-463&rft.issn=0302-766X&rft.eissn=1432-0878&rft_id=info:doi/10.1007/s00441-022-03645-6&rft_dat=%3Cgale_proqu%3EA715923394%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2708872066&rft_id=info:pmid/35688947&rft_galeid=A715923394&rfr_iscdi=true