Conditional Sox9 ablation improves locomotor recovery after spinal cord injury by increasing reactive sprouting
The absence of axonal regeneration after spinal cord injury (SCI) has been attributed to the up-regulation of axon-repelling molecules, such as chondroitin sulfate proteoglycans (CSPGs) present in the glial scar that forms post-SCI. We previously identified the transcription factor SOX9 as a key up-...
Gespeichert in:
Veröffentlicht in: | Experimental neurology 2016-09, Vol.283 (Pt A), p.1-15 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 15 |
---|---|
container_issue | Pt A |
container_start_page | 1 |
container_title | Experimental neurology |
container_volume | 283 |
creator | McKillop, William M. York, Elisa M. Rubinger, Luc Liu, Tony Ossowski, Natalie M. Xu, Kathy Hryciw, Todd Brown, Arthur |
description | The absence of axonal regeneration after spinal cord injury (SCI) has been attributed to the up-regulation of axon-repelling molecules, such as chondroitin sulfate proteoglycans (CSPGs) present in the glial scar that forms post-SCI. We previously identified the transcription factor SOX9 as a key up-regulator of CSPG production and also demonstrated that conditional Sox9 ablation leads to decreased CSPG levels and improved recovery of hind limb function after SCI. We herein demonstrate increased neural input onto spinal neurons caudal to the lesion in spinal cord injured Sox9 conditional knock out mice as indicated by increased levels of the presynaptic markers synaptophysin and vesicular glutamate transporter 1 (VGLUT1) compared to controls. Axonal sparing, long-range axonal regeneration and reactive sprouting were investigated as possible explanations for the increase in neural inputs caudal to the lesion and for the improved locomotor outcomes in spinal cord-injured Sox9 conditional knock out mice. Whereas retrograde tract-tracing studies failed to reveal any evidence for increased axonal sparing or for long-range regeneration in the Sox9 conditional knock out mice, anterograde tract-tracing experiments demonstrated increased reactive sprouting caudal to the lesion after SCI. Finally we demonstrate that application of a broad spectrum MMP inhibitor to reduce CSPG degradation in Sox9 conditional knock out mice prevents the improvements in locomotor recovery observed in untreated Sox9 conditional knock out mice. These results suggest that improved recovery of locomotor function in Sox9 conditional knock out mice after SCI is due to increased reactive sprouting secondary to reduced CSPG levels distal to the lesion.
•Cord-injured Sox9 knock outs recover more inputs caudal to the lesion than controls.•The increased neural inputs are not due to increased sparing or regeneration.•Sox9 knock out mice have more reactive sprouting than controls.•Doxycycline stabilizes CSPG levels and diminishes locomotor recovery in these mice. |
doi_str_mv | 10.1016/j.expneurol.2016.05.028 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1813627334</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0014488616301467</els_id><sourcerecordid>1813627334</sourcerecordid><originalsourceid>FETCH-LOGICAL-c371t-5063cb68518cd2bcb29724b69b9acc8c7962b15351fee2055f6877a8f471dd1b3</originalsourceid><addsrcrecordid>eNqFkM1PwyAchonRuDn9F7RHL618lEKPZvErWeJBPROgvxqWtkxoF_ffyzLd1RPw8vx4w4PQDcEFwaS6WxfwvRlgCr4raAoKzAtM5QmaE1zjnJYMn6I5xqTMSymrGbqIcY0xrksqztGMCsp4zdgc-aUfGjc6P-gue_PfdaZNp_fnzPWb4LcQs85b3_vRhyyATUnYZbodIWRx4_Zj1ocmc8N6Shdml3Y2gI5u-Ey8tqPbQiKDn8YUXaKzVncRrn7XBfp4fHhfPuer16eX5f0qt0yQMee4YtZUkhNpG2qsobWgpalqU2trpRV1RQ3hjJMWgGLO20oKoWVbCtI0xLAFuj28m4q_Joij6l200HV6AD9FRSRhFRWMlQkVB9QGH2OAVm2C63XYKYLV3rZaq6NttbetMFfJdpq8_i2ZTA_Nce5PbwLuDwCkr24dBBWtg8FC45LKUTXe_VvyA_49mBY</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1813627334</pqid></control><display><type>article</type><title>Conditional Sox9 ablation improves locomotor recovery after spinal cord injury by increasing reactive sprouting</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>McKillop, William M. ; York, Elisa M. ; Rubinger, Luc ; Liu, Tony ; Ossowski, Natalie M. ; Xu, Kathy ; Hryciw, Todd ; Brown, Arthur</creator><creatorcontrib>McKillop, William M. ; York, Elisa M. ; Rubinger, Luc ; Liu, Tony ; Ossowski, Natalie M. ; Xu, Kathy ; Hryciw, Todd ; Brown, Arthur</creatorcontrib><description>The absence of axonal regeneration after spinal cord injury (SCI) has been attributed to the up-regulation of axon-repelling molecules, such as chondroitin sulfate proteoglycans (CSPGs) present in the glial scar that forms post-SCI. We previously identified the transcription factor SOX9 as a key up-regulator of CSPG production and also demonstrated that conditional Sox9 ablation leads to decreased CSPG levels and improved recovery of hind limb function after SCI. We herein demonstrate increased neural input onto spinal neurons caudal to the lesion in spinal cord injured Sox9 conditional knock out mice as indicated by increased levels of the presynaptic markers synaptophysin and vesicular glutamate transporter 1 (VGLUT1) compared to controls. Axonal sparing, long-range axonal regeneration and reactive sprouting were investigated as possible explanations for the increase in neural inputs caudal to the lesion and for the improved locomotor outcomes in spinal cord-injured Sox9 conditional knock out mice. Whereas retrograde tract-tracing studies failed to reveal any evidence for increased axonal sparing or for long-range regeneration in the Sox9 conditional knock out mice, anterograde tract-tracing experiments demonstrated increased reactive sprouting caudal to the lesion after SCI. Finally we demonstrate that application of a broad spectrum MMP inhibitor to reduce CSPG degradation in Sox9 conditional knock out mice prevents the improvements in locomotor recovery observed in untreated Sox9 conditional knock out mice. These results suggest that improved recovery of locomotor function in Sox9 conditional knock out mice after SCI is due to increased reactive sprouting secondary to reduced CSPG levels distal to the lesion.
•Cord-injured Sox9 knock outs recover more inputs caudal to the lesion than controls.•The increased neural inputs are not due to increased sparing or regeneration.•Sox9 knock out mice have more reactive sprouting than controls.•Doxycycline stabilizes CSPG levels and diminishes locomotor recovery in these mice.</description><identifier>ISSN: 0014-4886</identifier><identifier>EISSN: 1090-2430</identifier><identifier>DOI: 10.1016/j.expneurol.2016.05.028</identifier><identifier>PMID: 27235933</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Axons - drug effects ; Axons - pathology ; Biotin - analogs & derivatives ; Biotin - pharmacokinetics ; Chondroitin Sulfate Proteoglycans - genetics ; Chondroitin Sulfate Proteoglycans - metabolism ; CSPG ; Dextrans - pharmacokinetics ; Disease Models, Animal ; Doxycycline - pharmacology ; Doxycycline - therapeutic use ; Edema - etiology ; Enzyme Inhibitors - pharmacology ; Enzyme Inhibitors - therapeutic use ; Humans ; Locomotion - genetics ; Locomotion - physiology ; Mice ; Nerve Tissue Proteins - metabolism ; Neuroplasticity ; Perineuronal nets ; Reactive sprouting ; Receptors, Estrogen - genetics ; Receptors, Estrogen - metabolism ; Recovery of Function - genetics ; Recovery of Function - physiology ; SOX9 ; SOX9 Transcription Factor - genetics ; SOX9 Transcription Factor - metabolism ; Spinal Cord Injuries - drug therapy ; Spinal Cord Injuries - genetics ; Spinal Cord Injuries - pathology ; Spinal Cord Injuries - physiopathology ; Spinal cord injury ; Stilbamidines - pharmacokinetics ; Synaptophysin - genetics ; Synaptophysin - metabolism ; Time Factors ; Up-Regulation - genetics ; Vesicular Glutamate Transport Protein 1 - genetics ; Vesicular Glutamate Transport Protein 1 - metabolism</subject><ispartof>Experimental neurology, 2016-09, Vol.283 (Pt A), p.1-15</ispartof><rights>2016 Elsevier Inc.</rights><rights>Copyright © 2016 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c371t-5063cb68518cd2bcb29724b69b9acc8c7962b15351fee2055f6877a8f471dd1b3</citedby><cites>FETCH-LOGICAL-c371t-5063cb68518cd2bcb29724b69b9acc8c7962b15351fee2055f6877a8f471dd1b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0014488616301467$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27235933$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>McKillop, William M.</creatorcontrib><creatorcontrib>York, Elisa M.</creatorcontrib><creatorcontrib>Rubinger, Luc</creatorcontrib><creatorcontrib>Liu, Tony</creatorcontrib><creatorcontrib>Ossowski, Natalie M.</creatorcontrib><creatorcontrib>Xu, Kathy</creatorcontrib><creatorcontrib>Hryciw, Todd</creatorcontrib><creatorcontrib>Brown, Arthur</creatorcontrib><title>Conditional Sox9 ablation improves locomotor recovery after spinal cord injury by increasing reactive sprouting</title><title>Experimental neurology</title><addtitle>Exp Neurol</addtitle><description>The absence of axonal regeneration after spinal cord injury (SCI) has been attributed to the up-regulation of axon-repelling molecules, such as chondroitin sulfate proteoglycans (CSPGs) present in the glial scar that forms post-SCI. We previously identified the transcription factor SOX9 as a key up-regulator of CSPG production and also demonstrated that conditional Sox9 ablation leads to decreased CSPG levels and improved recovery of hind limb function after SCI. We herein demonstrate increased neural input onto spinal neurons caudal to the lesion in spinal cord injured Sox9 conditional knock out mice as indicated by increased levels of the presynaptic markers synaptophysin and vesicular glutamate transporter 1 (VGLUT1) compared to controls. Axonal sparing, long-range axonal regeneration and reactive sprouting were investigated as possible explanations for the increase in neural inputs caudal to the lesion and for the improved locomotor outcomes in spinal cord-injured Sox9 conditional knock out mice. Whereas retrograde tract-tracing studies failed to reveal any evidence for increased axonal sparing or for long-range regeneration in the Sox9 conditional knock out mice, anterograde tract-tracing experiments demonstrated increased reactive sprouting caudal to the lesion after SCI. Finally we demonstrate that application of a broad spectrum MMP inhibitor to reduce CSPG degradation in Sox9 conditional knock out mice prevents the improvements in locomotor recovery observed in untreated Sox9 conditional knock out mice. These results suggest that improved recovery of locomotor function in Sox9 conditional knock out mice after SCI is due to increased reactive sprouting secondary to reduced CSPG levels distal to the lesion.
•Cord-injured Sox9 knock outs recover more inputs caudal to the lesion than controls.•The increased neural inputs are not due to increased sparing or regeneration.•Sox9 knock out mice have more reactive sprouting than controls.•Doxycycline stabilizes CSPG levels and diminishes locomotor recovery in these mice.</description><subject>Animals</subject><subject>Axons - drug effects</subject><subject>Axons - pathology</subject><subject>Biotin - analogs & derivatives</subject><subject>Biotin - pharmacokinetics</subject><subject>Chondroitin Sulfate Proteoglycans - genetics</subject><subject>Chondroitin Sulfate Proteoglycans - metabolism</subject><subject>CSPG</subject><subject>Dextrans - pharmacokinetics</subject><subject>Disease Models, Animal</subject><subject>Doxycycline - pharmacology</subject><subject>Doxycycline - therapeutic use</subject><subject>Edema - etiology</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Enzyme Inhibitors - therapeutic use</subject><subject>Humans</subject><subject>Locomotion - genetics</subject><subject>Locomotion - physiology</subject><subject>Mice</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Neuroplasticity</subject><subject>Perineuronal nets</subject><subject>Reactive sprouting</subject><subject>Receptors, Estrogen - genetics</subject><subject>Receptors, Estrogen - metabolism</subject><subject>Recovery of Function - genetics</subject><subject>Recovery of Function - physiology</subject><subject>SOX9</subject><subject>SOX9 Transcription Factor - genetics</subject><subject>SOX9 Transcription Factor - metabolism</subject><subject>Spinal Cord Injuries - drug therapy</subject><subject>Spinal Cord Injuries - genetics</subject><subject>Spinal Cord Injuries - pathology</subject><subject>Spinal Cord Injuries - physiopathology</subject><subject>Spinal cord injury</subject><subject>Stilbamidines - pharmacokinetics</subject><subject>Synaptophysin - genetics</subject><subject>Synaptophysin - metabolism</subject><subject>Time Factors</subject><subject>Up-Regulation - genetics</subject><subject>Vesicular Glutamate Transport Protein 1 - genetics</subject><subject>Vesicular Glutamate Transport Protein 1 - metabolism</subject><issn>0014-4886</issn><issn>1090-2430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1PwyAchonRuDn9F7RHL618lEKPZvErWeJBPROgvxqWtkxoF_ffyzLd1RPw8vx4w4PQDcEFwaS6WxfwvRlgCr4raAoKzAtM5QmaE1zjnJYMn6I5xqTMSymrGbqIcY0xrksqztGMCsp4zdgc-aUfGjc6P-gue_PfdaZNp_fnzPWb4LcQs85b3_vRhyyATUnYZbodIWRx4_Zj1ocmc8N6Shdml3Y2gI5u-Ey8tqPbQiKDn8YUXaKzVncRrn7XBfp4fHhfPuer16eX5f0qt0yQMee4YtZUkhNpG2qsobWgpalqU2trpRV1RQ3hjJMWgGLO20oKoWVbCtI0xLAFuj28m4q_Joij6l200HV6AD9FRSRhFRWMlQkVB9QGH2OAVm2C63XYKYLV3rZaq6NttbetMFfJdpq8_i2ZTA_Nce5PbwLuDwCkr24dBBWtg8FC45LKUTXe_VvyA_49mBY</recordid><startdate>201609</startdate><enddate>201609</enddate><creator>McKillop, William M.</creator><creator>York, Elisa M.</creator><creator>Rubinger, Luc</creator><creator>Liu, Tony</creator><creator>Ossowski, Natalie M.</creator><creator>Xu, Kathy</creator><creator>Hryciw, Todd</creator><creator>Brown, Arthur</creator><general>Elsevier Inc</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>7X8</scope></search><sort><creationdate>201609</creationdate><title>Conditional Sox9 ablation improves locomotor recovery after spinal cord injury by increasing reactive sprouting</title><author>McKillop, William M. ; York, Elisa M. ; Rubinger, Luc ; Liu, Tony ; Ossowski, Natalie M. ; Xu, Kathy ; Hryciw, Todd ; Brown, Arthur</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c371t-5063cb68518cd2bcb29724b69b9acc8c7962b15351fee2055f6877a8f471dd1b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Axons - drug effects</topic><topic>Axons - pathology</topic><topic>Biotin - analogs & derivatives</topic><topic>Biotin - pharmacokinetics</topic><topic>Chondroitin Sulfate Proteoglycans - genetics</topic><topic>Chondroitin Sulfate Proteoglycans - metabolism</topic><topic>CSPG</topic><topic>Dextrans - pharmacokinetics</topic><topic>Disease Models, Animal</topic><topic>Doxycycline - pharmacology</topic><topic>Doxycycline - therapeutic use</topic><topic>Edema - etiology</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Enzyme Inhibitors - therapeutic use</topic><topic>Humans</topic><topic>Locomotion - genetics</topic><topic>Locomotion - physiology</topic><topic>Mice</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Neuroplasticity</topic><topic>Perineuronal nets</topic><topic>Reactive sprouting</topic><topic>Receptors, Estrogen - genetics</topic><topic>Receptors, Estrogen - metabolism</topic><topic>Recovery of Function - genetics</topic><topic>Recovery of Function - physiology</topic><topic>SOX9</topic><topic>SOX9 Transcription Factor - genetics</topic><topic>SOX9 Transcription Factor - metabolism</topic><topic>Spinal Cord Injuries - drug therapy</topic><topic>Spinal Cord Injuries - genetics</topic><topic>Spinal Cord Injuries - pathology</topic><topic>Spinal Cord Injuries - physiopathology</topic><topic>Spinal cord injury</topic><topic>Stilbamidines - pharmacokinetics</topic><topic>Synaptophysin - genetics</topic><topic>Synaptophysin - metabolism</topic><topic>Time Factors</topic><topic>Up-Regulation - genetics</topic><topic>Vesicular Glutamate Transport Protein 1 - genetics</topic><topic>Vesicular Glutamate Transport Protein 1 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McKillop, William M.</creatorcontrib><creatorcontrib>York, Elisa M.</creatorcontrib><creatorcontrib>Rubinger, Luc</creatorcontrib><creatorcontrib>Liu, Tony</creatorcontrib><creatorcontrib>Ossowski, Natalie M.</creatorcontrib><creatorcontrib>Xu, Kathy</creatorcontrib><creatorcontrib>Hryciw, Todd</creatorcontrib><creatorcontrib>Brown, Arthur</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</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>McKillop, William M.</au><au>York, Elisa M.</au><au>Rubinger, Luc</au><au>Liu, Tony</au><au>Ossowski, Natalie M.</au><au>Xu, Kathy</au><au>Hryciw, Todd</au><au>Brown, Arthur</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Conditional Sox9 ablation improves locomotor recovery after spinal cord injury by increasing reactive sprouting</atitle><jtitle>Experimental neurology</jtitle><addtitle>Exp Neurol</addtitle><date>2016-09</date><risdate>2016</risdate><volume>283</volume><issue>Pt A</issue><spage>1</spage><epage>15</epage><pages>1-15</pages><issn>0014-4886</issn><eissn>1090-2430</eissn><abstract>The absence of axonal regeneration after spinal cord injury (SCI) has been attributed to the up-regulation of axon-repelling molecules, such as chondroitin sulfate proteoglycans (CSPGs) present in the glial scar that forms post-SCI. We previously identified the transcription factor SOX9 as a key up-regulator of CSPG production and also demonstrated that conditional Sox9 ablation leads to decreased CSPG levels and improved recovery of hind limb function after SCI. We herein demonstrate increased neural input onto spinal neurons caudal to the lesion in spinal cord injured Sox9 conditional knock out mice as indicated by increased levels of the presynaptic markers synaptophysin and vesicular glutamate transporter 1 (VGLUT1) compared to controls. Axonal sparing, long-range axonal regeneration and reactive sprouting were investigated as possible explanations for the increase in neural inputs caudal to the lesion and for the improved locomotor outcomes in spinal cord-injured Sox9 conditional knock out mice. Whereas retrograde tract-tracing studies failed to reveal any evidence for increased axonal sparing or for long-range regeneration in the Sox9 conditional knock out mice, anterograde tract-tracing experiments demonstrated increased reactive sprouting caudal to the lesion after SCI. Finally we demonstrate that application of a broad spectrum MMP inhibitor to reduce CSPG degradation in Sox9 conditional knock out mice prevents the improvements in locomotor recovery observed in untreated Sox9 conditional knock out mice. These results suggest that improved recovery of locomotor function in Sox9 conditional knock out mice after SCI is due to increased reactive sprouting secondary to reduced CSPG levels distal to the lesion.
•Cord-injured Sox9 knock outs recover more inputs caudal to the lesion than controls.•The increased neural inputs are not due to increased sparing or regeneration.•Sox9 knock out mice have more reactive sprouting than controls.•Doxycycline stabilizes CSPG levels and diminishes locomotor recovery in these mice.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>27235933</pmid><doi>10.1016/j.expneurol.2016.05.028</doi><tpages>15</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0014-4886 |
ispartof | Experimental neurology, 2016-09, Vol.283 (Pt A), p.1-15 |
issn | 0014-4886 1090-2430 |
language | eng |
recordid | cdi_proquest_miscellaneous_1813627334 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Animals Axons - drug effects Axons - pathology Biotin - analogs & derivatives Biotin - pharmacokinetics Chondroitin Sulfate Proteoglycans - genetics Chondroitin Sulfate Proteoglycans - metabolism CSPG Dextrans - pharmacokinetics Disease Models, Animal Doxycycline - pharmacology Doxycycline - therapeutic use Edema - etiology Enzyme Inhibitors - pharmacology Enzyme Inhibitors - therapeutic use Humans Locomotion - genetics Locomotion - physiology Mice Nerve Tissue Proteins - metabolism Neuroplasticity Perineuronal nets Reactive sprouting Receptors, Estrogen - genetics Receptors, Estrogen - metabolism Recovery of Function - genetics Recovery of Function - physiology SOX9 SOX9 Transcription Factor - genetics SOX9 Transcription Factor - metabolism Spinal Cord Injuries - drug therapy Spinal Cord Injuries - genetics Spinal Cord Injuries - pathology Spinal Cord Injuries - physiopathology Spinal cord injury Stilbamidines - pharmacokinetics Synaptophysin - genetics Synaptophysin - metabolism Time Factors Up-Regulation - genetics Vesicular Glutamate Transport Protein 1 - genetics Vesicular Glutamate Transport Protein 1 - metabolism |
title | Conditional Sox9 ablation improves locomotor recovery after spinal cord injury by increasing reactive sprouting |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T07%3A46%3A58IST&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=Conditional%20Sox9%20ablation%20improves%20locomotor%20recovery%20after%20spinal%20cord%20injury%20by%20increasing%20reactive%20sprouting&rft.jtitle=Experimental%20neurology&rft.au=McKillop,%20William%20M.&rft.date=2016-09&rft.volume=283&rft.issue=Pt%20A&rft.spage=1&rft.epage=15&rft.pages=1-15&rft.issn=0014-4886&rft.eissn=1090-2430&rft_id=info:doi/10.1016/j.expneurol.2016.05.028&rft_dat=%3Cproquest_cross%3E1813627334%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=1813627334&rft_id=info:pmid/27235933&rft_els_id=S0014488616301467&rfr_iscdi=true |