Source:http://linkedlifedata.com/resource/pubmed/id/16889522
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
7
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pubmed:dateCreated |
2006-8-7
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pubmed:abstractText |
To obtain a valuable treatment of congenital muscle defect, cell-matrix constructs composed of satellite cell-derived myoblasts (XY karyotype) seeded on muscle acellular matrices were used to repair a previously created full-thickness defect of abdominal wall of 18 1-month-old female Lewis rats. Acellular abdominal matrices, obtained by a detergent-enzymatic method, were positive for both basic fibroblast growth factor and transforming growth factor-beta, and were able to support in vitro cell adhesion. All animals survived the surgery, without signs of infection or implant rejection, and were humanely killed at 1, 3, or 9 months after surgery. The implants appeared well preserved, were integrated in the host tissue, and maintained their original dimension and thickness until 9 months. Vesicular acetylcholine transporter was expressed on the surface of muscle fibers from 1 month postsurgery. Finally, implanted male myoblasts were present inside the patches until 9 months, as demonstrated by the expression of SrY mRNA and by the presence of Y chromosome probe signal. These results allow us to conclude that cell-matrix constructs could represent a promising approach to the repair of muscle defects, because they are repopulated in vivo by skeletal muscle cells and nervous elements and maintain their structural integrity over the long term.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Biocompatible Materials,
http://linkedlifedata.com/resource/pubmed/chemical/Fibroblast Growth Factor 2,
http://linkedlifedata.com/resource/pubmed/chemical/Sex-Determining Region Y Protein,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1076-3279
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
12
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1929-36
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:16889522-Abdominal Muscles,
pubmed-meshheading:16889522-Animals,
pubmed-meshheading:16889522-Biocompatible Materials,
pubmed-meshheading:16889522-Bioprosthesis,
pubmed-meshheading:16889522-Extracellular Matrix,
pubmed-meshheading:16889522-Female,
pubmed-meshheading:16889522-Fibroblast Growth Factor 2,
pubmed-meshheading:16889522-Implants, Experimental,
pubmed-meshheading:16889522-Male,
pubmed-meshheading:16889522-Muscle Fibers, Skeletal,
pubmed-meshheading:16889522-Rats,
pubmed-meshheading:16889522-Rats, Inbred Lew,
pubmed-meshheading:16889522-Sex-Determining Region Y Protein,
pubmed-meshheading:16889522-Time Factors,
pubmed-meshheading:16889522-Tissue Engineering,
pubmed-meshheading:16889522-Transforming Growth Factor beta,
pubmed-meshheading:16889522-Wound Healing
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pubmed:year |
2006
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pubmed:articleTitle |
Myoblast-acellular skeletal muscle matrix constructs guarantee a long-term repair of experimental full-thickness abdominal wall defects.
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pubmed:affiliation |
Department of Pediatrics, Division of Pediatric Surgery, University of Padua, Padua, Italy.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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