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rdf:type |
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lifeskim:mentions |
umls-concept:C0001675,
umls-concept:C0004112,
umls-concept:C0009938,
umls-concept:C0017262,
umls-concept:C0018956,
umls-concept:C0028944,
umls-concept:C0037925,
umls-concept:C0053932,
umls-concept:C0185117,
umls-concept:C1656972,
umls-concept:C2911684
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pubmed:issue |
16
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pubmed:dateCreated |
2011-4-21
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pubmed:abstractText |
Promotion of remyelination is an important therapeutic strategy to facilitate functional recovery after traumatic spinal cord injury (SCI). Transplantation of neural stem cells (NSCs) or oligodendrocyte precursor cells (OPCs) has been used to enhance remyelination after SCI. However, the microenvironment in the injured spinal cord is inhibitory for oligodendrocyte (OL) differentiation of NSCs or OPCs. Identifying the signaling pathways that inhibit OL differentiation in the injured spinal cord could lead to new therapeutic strategies to enhance remyelination and functional recovery after SCI. In the present study, we show that reactive astrocytes from the injured rat spinal cord or their conditioned media inhibit OL differentiation of adult OPCs with concurrent promotion of astrocyte differentiation. The expression of bone morphogenetic proteins (BMP) is dramatically increased in the reactive astrocytes and their conditioned media. Importantly, blocking BMP activity by BMP receptor antagonist, noggin, reverse the effects of active astrocytes on OPC differentiation by increasing the differentiation of OL from OPCs while decreasing the generation of astrocytes. These data indicate that the upregulated bone morphogenetic proteins in the reactive astrocytes are major factors to inhibit OL differentiation of OPCs and to promote its astrocyte differentiation. These data suggest that manipulation of BMP signaling in the endogenous or grafted NSCs or OPCs may be a useful therapeutic strategy to increase their OL differentiation and remyelination and enhance functional recovery after SCI.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-10491262,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-11076675,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-11796850,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-11844734,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-12357247,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-12399304,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-14576772,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-14769388,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-15048925,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-15276151,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-15296834,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-15699059,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-15888645,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-16086023,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-16543131,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-16753227,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-16921543,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-17696121,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-17722066,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-17872503,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-18232014,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-18558855,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-18567922,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-18931697,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-19371354,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-8893019,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-9151728,
http://linkedlifedata.com/resource/pubmed/commentcorrection/21508230-9697852
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1529-2401
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
20
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6053-8
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pubmed:dateRevised |
2011-9-26
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pubmed:meshHeading |
pubmed-meshheading:21508230-Animals,
pubmed-meshheading:21508230-Astrocytes,
pubmed-meshheading:21508230-Blotting, Western,
pubmed-meshheading:21508230-Bone Morphogenetic Proteins,
pubmed-meshheading:21508230-Cell Differentiation,
pubmed-meshheading:21508230-Cells, Cultured,
pubmed-meshheading:21508230-Coculture Techniques,
pubmed-meshheading:21508230-Fluorescent Antibody Technique,
pubmed-meshheading:21508230-Glial Fibrillary Acidic Protein,
pubmed-meshheading:21508230-Oligodendroglia,
pubmed-meshheading:21508230-Rats,
pubmed-meshheading:21508230-Signal Transduction,
pubmed-meshheading:21508230-Spinal Cord,
pubmed-meshheading:21508230-Spinal Cord Injuries,
pubmed-meshheading:21508230-Stem Cells
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pubmed:year |
2011
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pubmed:articleTitle |
Astrocytes from the contused spinal cord inhibit oligodendrocyte differentiation of adult oligodendrocyte precursor cells by increasing the expression of bone morphogenetic proteins.
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pubmed:affiliation |
Kentucky Spinal Cord Injury Research Center, Department of Neurological Surgery, University of Louisville School of Medicine, Louisville, Kentucky 40202, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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