Ferroptosis in the neurovascular unit after spinal cord injury
The mechanisms of secondary injury following spinal cord injury are complicated. The role of ferroptosis, which is a newly discovered form of regulated cell death in the neurovascular unit(NVU), is increasingly important. Ferroptosis inhibitors have been shown to improve neurovascular homeostasis an...
Gespeichert in:
Veröffentlicht in: | Experimental neurology 2024-11, Vol.381, p.114943, Article 114943 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | |
container_start_page | 114943 |
container_title | Experimental neurology |
container_volume | 381 |
creator | Huang, Yushan Bai, Jinzhu |
description | The mechanisms of secondary injury following spinal cord injury are complicated. The role of ferroptosis, which is a newly discovered form of regulated cell death in the neurovascular unit(NVU), is increasingly important. Ferroptosis inhibitors have been shown to improve neurovascular homeostasis and attenuate secondary spinal cord injury(SCI). This review focuses on the mechanisms of ferroptosis in NVU cells and NVU-targeted therapeutic strategies according to the stages of SCI, and analyzes possible future research directions. |
doi_str_mv | 10.1016/j.expneurol.2024.114943 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3101794120</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0014488624002693</els_id><sourcerecordid>3101794120</sourcerecordid><originalsourceid>FETCH-LOGICAL-c247t-83754492604793edc4431882a135c4a9165d7df51261675636a7d38952c591c63</originalsourceid><addsrcrecordid>eNqFkD1PwzAURS0EoqXwFyAjS4K_YscLUlVRQKrEArNlnBfhKI2DnVTw70lJ6cr0lnPv1TsI3RCcEUzEXZ3BV9fCEHyTUUx5RghXnJ2gOcEKp5QzfIrmGBOe8qIQM3QRY40xVpzKczRjinKKhZqj-zWE4LveRxcT1yb9ByS_vTsT7dCYkAyt6xNT9RCS2LnWNIn1oRzZegjfl-isMk2Eq8NdoLf1w-vqKd28PD6vlpvUUi77tGAy51xRgblUDErLOSNFQQ1hueVGEZGXsqxyQgURMhdMGFmyQuXU5opYwRbodurtgv8cIPZ666KFpjEt-CFqNlqRihOKR1ROqA0-xgCV7oLbmvCtCdZ7ebrWR3l6L09P8sbk9WFkeN9Cecz92RqB5QTA-OrOQdDROmgtlC6A7XXp3b8jP-75gvU</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3101794120</pqid></control><display><type>article</type><title>Ferroptosis in the neurovascular unit after spinal cord injury</title><source>Access via ScienceDirect (Elsevier)</source><creator>Huang, Yushan ; Bai, Jinzhu</creator><creatorcontrib>Huang, Yushan ; Bai, Jinzhu</creatorcontrib><description>The mechanisms of secondary injury following spinal cord injury are complicated. The role of ferroptosis, which is a newly discovered form of regulated cell death in the neurovascular unit(NVU), is increasingly important. Ferroptosis inhibitors have been shown to improve neurovascular homeostasis and attenuate secondary spinal cord injury(SCI). This review focuses on the mechanisms of ferroptosis in NVU cells and NVU-targeted therapeutic strategies according to the stages of SCI, and analyzes possible future research directions.</description><identifier>ISSN: 0014-4886</identifier><identifier>ISSN: 1090-2430</identifier><identifier>EISSN: 1090-2430</identifier><identifier>DOI: 10.1016/j.expneurol.2024.114943</identifier><identifier>PMID: 39242069</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Ferroptosis ; Neurovascular unit ; Secondary injury ; Spinal cord injury</subject><ispartof>Experimental neurology, 2024-11, Vol.381, p.114943, Article 114943</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024. Published by Elsevier Inc.</rights><rights>Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c247t-83754492604793edc4431882a135c4a9165d7df51261675636a7d38952c591c63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.expneurol.2024.114943$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39242069$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Yushan</creatorcontrib><creatorcontrib>Bai, Jinzhu</creatorcontrib><title>Ferroptosis in the neurovascular unit after spinal cord injury</title><title>Experimental neurology</title><addtitle>Exp Neurol</addtitle><description>The mechanisms of secondary injury following spinal cord injury are complicated. The role of ferroptosis, which is a newly discovered form of regulated cell death in the neurovascular unit(NVU), is increasingly important. Ferroptosis inhibitors have been shown to improve neurovascular homeostasis and attenuate secondary spinal cord injury(SCI). This review focuses on the mechanisms of ferroptosis in NVU cells and NVU-targeted therapeutic strategies according to the stages of SCI, and analyzes possible future research directions.</description><subject>Ferroptosis</subject><subject>Neurovascular unit</subject><subject>Secondary injury</subject><subject>Spinal cord injury</subject><issn>0014-4886</issn><issn>1090-2430</issn><issn>1090-2430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkD1PwzAURS0EoqXwFyAjS4K_YscLUlVRQKrEArNlnBfhKI2DnVTw70lJ6cr0lnPv1TsI3RCcEUzEXZ3BV9fCEHyTUUx5RghXnJ2gOcEKp5QzfIrmGBOe8qIQM3QRY40xVpzKczRjinKKhZqj-zWE4LveRxcT1yb9ByS_vTsT7dCYkAyt6xNT9RCS2LnWNIn1oRzZegjfl-isMk2Eq8NdoLf1w-vqKd28PD6vlpvUUi77tGAy51xRgblUDErLOSNFQQ1hueVGEZGXsqxyQgURMhdMGFmyQuXU5opYwRbodurtgv8cIPZ666KFpjEt-CFqNlqRihOKR1ROqA0-xgCV7oLbmvCtCdZ7ebrWR3l6L09P8sbk9WFkeN9Cecz92RqB5QTA-OrOQdDROmgtlC6A7XXp3b8jP-75gvU</recordid><startdate>20241101</startdate><enddate>20241101</enddate><creator>Huang, Yushan</creator><creator>Bai, Jinzhu</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20241101</creationdate><title>Ferroptosis in the neurovascular unit after spinal cord injury</title><author>Huang, Yushan ; Bai, Jinzhu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c247t-83754492604793edc4431882a135c4a9165d7df51261675636a7d38952c591c63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Ferroptosis</topic><topic>Neurovascular unit</topic><topic>Secondary injury</topic><topic>Spinal cord injury</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Yushan</creatorcontrib><creatorcontrib>Bai, Jinzhu</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Yushan</au><au>Bai, Jinzhu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ferroptosis in the neurovascular unit after spinal cord injury</atitle><jtitle>Experimental neurology</jtitle><addtitle>Exp Neurol</addtitle><date>2024-11-01</date><risdate>2024</risdate><volume>381</volume><spage>114943</spage><pages>114943-</pages><artnum>114943</artnum><issn>0014-4886</issn><issn>1090-2430</issn><eissn>1090-2430</eissn><abstract>The mechanisms of secondary injury following spinal cord injury are complicated. The role of ferroptosis, which is a newly discovered form of regulated cell death in the neurovascular unit(NVU), is increasingly important. Ferroptosis inhibitors have been shown to improve neurovascular homeostasis and attenuate secondary spinal cord injury(SCI). This review focuses on the mechanisms of ferroptosis in NVU cells and NVU-targeted therapeutic strategies according to the stages of SCI, and analyzes possible future research directions.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>39242069</pmid><doi>10.1016/j.expneurol.2024.114943</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0014-4886 |
ispartof | Experimental neurology, 2024-11, Vol.381, p.114943, Article 114943 |
issn | 0014-4886 1090-2430 1090-2430 |
language | eng |
recordid | cdi_proquest_miscellaneous_3101794120 |
source | Access via ScienceDirect (Elsevier) |
subjects | Ferroptosis Neurovascular unit Secondary injury Spinal cord injury |
title | Ferroptosis in the neurovascular unit after spinal cord injury |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T13%3A11%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ferroptosis%20in%20the%20neurovascular%20unit%20after%20spinal%20cord%20injury&rft.jtitle=Experimental%20neurology&rft.au=Huang,%20Yushan&rft.date=2024-11-01&rft.volume=381&rft.spage=114943&rft.pages=114943-&rft.artnum=114943&rft.issn=0014-4886&rft.eissn=1090-2430&rft_id=info:doi/10.1016/j.expneurol.2024.114943&rft_dat=%3Cproquest_cross%3E3101794120%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3101794120&rft_id=info:pmid/39242069&rft_els_id=S0014488624002693&rfr_iscdi=true |