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Human fetal neural stem cells grafted into contusion-injured rat spinal cords improve behavior
Grafted human neural stem cells (hNSCs) may help to alleviate functional deficits resulting from spinal cord injury by bridging gaps, replacing lost neurons or oligodendrocytes, and providing neurotrophic factors. Previously, we showed that primed hNSCs differentiated into cholinergic neurons in an...
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Published in: | Journal of neuroscience research 2007-01, Vol.85 (1), p.47-57 |
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creator | Tarasenko, Yevgeniya I. Gao, Junling Nie, Linghui Johnson, Kathia M. Grady, James J. Hulsebosch, Claire E. McAdoo, David J. Wu, Ping |
description | Grafted human neural stem cells (hNSCs) may help to alleviate functional deficits resulting from spinal cord injury by bridging gaps, replacing lost neurons or oligodendrocytes, and providing neurotrophic factors. Previously, we showed that primed hNSCs differentiated into cholinergic neurons in an intact spinal cord. In this study, we tested the fate of hNSCs transplanted into a spinal cord T10 contusion injury model. When grafted into injured spinal cords of adult male rats on either the same day or 3 or 9 days after a moderate contusion injury, both primed and unprimed hNSCs survived for 3 months postengraftment only in animals that received grafts at 9 days postinjury. Histological analyses revealed that primed hNSCs tended to survive better and differentiated at higher rates into neurons and oligodendrocytes than did unprimed counterparts. Furthermore, only primed cells gave rise to cholinergic neurons. Animals receiving primed hNSC grafts on the ninth day postcontusion improved trunk stability, as determined by rearing activity measurements 3 months after grafting. This study indicates that human neural stem cell fate determination in vivo is influenced by the predifferentiation stage of stem cells prior to grafting. Furthermore, stem cell‐mediated facilitation of functional improvement depends on the timing of transplantation after injury, the grafting sites, and the survival of newly differentiated neurons and oligodendrocytes. © 2006 Wiley‐Liss, Inc. |
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Previously, we showed that primed hNSCs differentiated into cholinergic neurons in an intact spinal cord. In this study, we tested the fate of hNSCs transplanted into a spinal cord T10 contusion injury model. When grafted into injured spinal cords of adult male rats on either the same day or 3 or 9 days after a moderate contusion injury, both primed and unprimed hNSCs survived for 3 months postengraftment only in animals that received grafts at 9 days postinjury. Histological analyses revealed that primed hNSCs tended to survive better and differentiated at higher rates into neurons and oligodendrocytes than did unprimed counterparts. Furthermore, only primed cells gave rise to cholinergic neurons. Animals receiving primed hNSC grafts on the ninth day postcontusion improved trunk stability, as determined by rearing activity measurements 3 months after grafting. This study indicates that human neural stem cell fate determination in vivo is influenced by the predifferentiation stage of stem cells prior to grafting. Furthermore, stem cell‐mediated facilitation of functional improvement depends on the timing of transplantation after injury, the grafting sites, and the survival of newly differentiated neurons and oligodendrocytes. © 2006 Wiley‐Liss, Inc.</description><identifier>ISSN: 0360-4012</identifier><identifier>EISSN: 1097-4547</identifier><identifier>DOI: 10.1002/jnr.21098</identifier><identifier>PMID: 17075895</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Behavior, Animal - physiology ; CD11b Antigen ; Cell Count - methods ; cell therapy ; Cells, Cultured ; Choline O-Acetyltransferase - metabolism ; cholinergic neurons ; Claudins ; differentiation ; Exploratory Behavior - physiology ; Fetus ; Glial Fibrillary Acidic Protein - metabolism ; Green Fluorescent Proteins - metabolism ; Humans ; Immunohistochemistry - methods ; Indoles ; Lysosomal-Associated Membrane Protein 2 - metabolism ; Male ; Motor Activity - physiology ; Nerve Tissue Proteins - metabolism ; Neurons - physiology ; Neurons - transplantation ; Rats ; Spinal Cord Injuries - physiopathology ; Spinal Cord Injuries - surgery ; Stem Cell Transplantation ; Stem Cells - physiology ; trans-plantation ; Transfection - methods ; Transplantation, Heterologous</subject><ispartof>Journal of neuroscience research, 2007-01, Vol.85 (1), p.47-57</ispartof><rights>Copyright © 2006 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3968-b44261eca63503bddb9f981d2dda76274c635644d71d80280237345fb1c207f3</citedby><cites>FETCH-LOGICAL-c3968-b44261eca63503bddb9f981d2dda76274c635644d71d80280237345fb1c207f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17075895$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tarasenko, Yevgeniya I.</creatorcontrib><creatorcontrib>Gao, Junling</creatorcontrib><creatorcontrib>Nie, Linghui</creatorcontrib><creatorcontrib>Johnson, Kathia M.</creatorcontrib><creatorcontrib>Grady, James J.</creatorcontrib><creatorcontrib>Hulsebosch, Claire E.</creatorcontrib><creatorcontrib>McAdoo, David J.</creatorcontrib><creatorcontrib>Wu, Ping</creatorcontrib><title>Human fetal neural stem cells grafted into contusion-injured rat spinal cords improve behavior</title><title>Journal of neuroscience research</title><addtitle>J. Neurosci. Res</addtitle><description>Grafted human neural stem cells (hNSCs) may help to alleviate functional deficits resulting from spinal cord injury by bridging gaps, replacing lost neurons or oligodendrocytes, and providing neurotrophic factors. Previously, we showed that primed hNSCs differentiated into cholinergic neurons in an intact spinal cord. In this study, we tested the fate of hNSCs transplanted into a spinal cord T10 contusion injury model. When grafted into injured spinal cords of adult male rats on either the same day or 3 or 9 days after a moderate contusion injury, both primed and unprimed hNSCs survived for 3 months postengraftment only in animals that received grafts at 9 days postinjury. Histological analyses revealed that primed hNSCs tended to survive better and differentiated at higher rates into neurons and oligodendrocytes than did unprimed counterparts. Furthermore, only primed cells gave rise to cholinergic neurons. Animals receiving primed hNSC grafts on the ninth day postcontusion improved trunk stability, as determined by rearing activity measurements 3 months after grafting. This study indicates that human neural stem cell fate determination in vivo is influenced by the predifferentiation stage of stem cells prior to grafting. Furthermore, stem cell‐mediated facilitation of functional improvement depends on the timing of transplantation after injury, the grafting sites, and the survival of newly differentiated neurons and oligodendrocytes. © 2006 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>Behavior, Animal - physiology</subject><subject>CD11b Antigen</subject><subject>Cell Count - methods</subject><subject>cell therapy</subject><subject>Cells, Cultured</subject><subject>Choline O-Acetyltransferase - metabolism</subject><subject>cholinergic neurons</subject><subject>Claudins</subject><subject>differentiation</subject><subject>Exploratory Behavior - physiology</subject><subject>Fetus</subject><subject>Glial Fibrillary Acidic Protein - metabolism</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Humans</subject><subject>Immunohistochemistry - methods</subject><subject>Indoles</subject><subject>Lysosomal-Associated Membrane Protein 2 - metabolism</subject><subject>Male</subject><subject>Motor Activity - physiology</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Neurons - physiology</subject><subject>Neurons - transplantation</subject><subject>Rats</subject><subject>Spinal Cord Injuries - physiopathology</subject><subject>Spinal Cord Injuries - surgery</subject><subject>Stem Cell Transplantation</subject><subject>Stem Cells - physiology</subject><subject>trans-plantation</subject><subject>Transfection - methods</subject><subject>Transplantation, Heterologous</subject><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp1kF1LwzAYhYMobk4v_AOSK8GLznw1aS9FdCpjigy8M6RNqpltOpPWj39v5qZeCS8cePOc85IDwCFGY4wQOV04PyYY5dkWGEYRCUuZ2AZDRDlKGMJkAPZCWCCE8jylu2CABRJplqdD8HjVN8rBynSqhs70PkroTANLU9cBPnlVdUZD67oWlq3r-mBbl1i36H1ce9XBsLQumsrW6wBts_Ttm4GFeVZvtvX7YKdSdTAHGx2B-eXF_Pwqmd5Ors_PpklJc54lBWOEY1MqTlNEC62LvMozrInWSnAiWBkfOGNaYJ0hEocKytKqwCVBoqIjcLyOjddfexM62diw-oFypu2D5BkVgqQsgidrsPRtCN5Uculto_ynxEiuupSxS_ndZWSPNqF90Rj9R27Ki8DpGni3tfn8P0nezO5_IpO1w8aOP34dyr9ILqhI5cNsIjGbXU7uKJcZ_QJ3C41T</recordid><startdate>200701</startdate><enddate>200701</enddate><creator>Tarasenko, Yevgeniya I.</creator><creator>Gao, Junling</creator><creator>Nie, Linghui</creator><creator>Johnson, Kathia M.</creator><creator>Grady, James J.</creator><creator>Hulsebosch, Claire E.</creator><creator>McAdoo, David J.</creator><creator>Wu, Ping</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><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>200701</creationdate><title>Human fetal neural stem cells grafted into contusion-injured rat spinal cords improve behavior</title><author>Tarasenko, Yevgeniya I. ; Gao, Junling ; Nie, Linghui ; Johnson, Kathia M. ; Grady, James J. ; Hulsebosch, Claire E. ; McAdoo, David J. ; Wu, Ping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3968-b44261eca63503bddb9f981d2dda76274c635644d71d80280237345fb1c207f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Animals</topic><topic>Behavior, Animal - physiology</topic><topic>CD11b Antigen</topic><topic>Cell Count - methods</topic><topic>cell therapy</topic><topic>Cells, Cultured</topic><topic>Choline O-Acetyltransferase - metabolism</topic><topic>cholinergic neurons</topic><topic>Claudins</topic><topic>differentiation</topic><topic>Exploratory Behavior - physiology</topic><topic>Fetus</topic><topic>Glial Fibrillary Acidic Protein - metabolism</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Humans</topic><topic>Immunohistochemistry - methods</topic><topic>Indoles</topic><topic>Lysosomal-Associated Membrane Protein 2 - metabolism</topic><topic>Male</topic><topic>Motor Activity - physiology</topic><topic>Nerve Tissue Proteins - metabolism</topic><topic>Neurons - physiology</topic><topic>Neurons - transplantation</topic><topic>Rats</topic><topic>Spinal Cord Injuries - physiopathology</topic><topic>Spinal Cord Injuries - surgery</topic><topic>Stem Cell Transplantation</topic><topic>Stem Cells - physiology</topic><topic>trans-plantation</topic><topic>Transfection - methods</topic><topic>Transplantation, Heterologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tarasenko, Yevgeniya I.</creatorcontrib><creatorcontrib>Gao, Junling</creatorcontrib><creatorcontrib>Nie, Linghui</creatorcontrib><creatorcontrib>Johnson, Kathia M.</creatorcontrib><creatorcontrib>Grady, James J.</creatorcontrib><creatorcontrib>Hulsebosch, Claire E.</creatorcontrib><creatorcontrib>McAdoo, David J.</creatorcontrib><creatorcontrib>Wu, Ping</creatorcontrib><collection>Istex</collection><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>Journal of neuroscience research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tarasenko, Yevgeniya I.</au><au>Gao, Junling</au><au>Nie, Linghui</au><au>Johnson, Kathia M.</au><au>Grady, James J.</au><au>Hulsebosch, Claire E.</au><au>McAdoo, David J.</au><au>Wu, Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human fetal neural stem cells grafted into contusion-injured rat spinal cords improve behavior</atitle><jtitle>Journal of neuroscience research</jtitle><addtitle>J. Neurosci. Res</addtitle><date>2007-01</date><risdate>2007</risdate><volume>85</volume><issue>1</issue><spage>47</spage><epage>57</epage><pages>47-57</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>Grafted human neural stem cells (hNSCs) may help to alleviate functional deficits resulting from spinal cord injury by bridging gaps, replacing lost neurons or oligodendrocytes, and providing neurotrophic factors. Previously, we showed that primed hNSCs differentiated into cholinergic neurons in an intact spinal cord. In this study, we tested the fate of hNSCs transplanted into a spinal cord T10 contusion injury model. When grafted into injured spinal cords of adult male rats on either the same day or 3 or 9 days after a moderate contusion injury, both primed and unprimed hNSCs survived for 3 months postengraftment only in animals that received grafts at 9 days postinjury. Histological analyses revealed that primed hNSCs tended to survive better and differentiated at higher rates into neurons and oligodendrocytes than did unprimed counterparts. Furthermore, only primed cells gave rise to cholinergic neurons. Animals receiving primed hNSC grafts on the ninth day postcontusion improved trunk stability, as determined by rearing activity measurements 3 months after grafting. This study indicates that human neural stem cell fate determination in vivo is influenced by the predifferentiation stage of stem cells prior to grafting. Furthermore, stem cell‐mediated facilitation of functional improvement depends on the timing of transplantation after injury, the grafting sites, and the survival of newly differentiated neurons and oligodendrocytes. © 2006 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17075895</pmid><doi>10.1002/jnr.21098</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Behavior, Animal - physiology CD11b Antigen Cell Count - methods cell therapy Cells, Cultured Choline O-Acetyltransferase - metabolism cholinergic neurons Claudins differentiation Exploratory Behavior - physiology Fetus Glial Fibrillary Acidic Protein - metabolism Green Fluorescent Proteins - metabolism Humans Immunohistochemistry - methods Indoles Lysosomal-Associated Membrane Protein 2 - metabolism Male Motor Activity - physiology Nerve Tissue Proteins - metabolism Neurons - physiology Neurons - transplantation Rats Spinal Cord Injuries - physiopathology Spinal Cord Injuries - surgery Stem Cell Transplantation Stem Cells - physiology trans-plantation Transfection - methods Transplantation, Heterologous |
title | Human fetal neural stem cells grafted into contusion-injured rat spinal cords improve behavior |
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