Source:http://linkedlifedata.com/resource/pubmed/id/11175789
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2001-2-22
|
pubmed:abstractText |
Aging skeletal muscles suffer a steady decline in mass and functional performance, and compromised muscle integrity as fibrotic invasions replace contractile tissue, accompanied by a characteristic loss in the fastest, most powerful muscle fibers. The same programmed deficits in muscle structure and function are found in numerous neurodegenerative syndromes and disease-related cachexia. We have generated a model of persistent, functional myocyte hypertrophy using a tissue-restricted transgene encoding a locally acting isoform of insulin-like growth factor-1 that is expressed in skeletal muscle (mIgf-1). Transgenic embryos developed normally, and postnatal increases in muscle mass and strength were not accompanied by the additional pathological changes seen in other Igf-1 transgenic models. Expression of GATA-2, a transcription factor normally undetected in skeletal muscle, marked hypertrophic myocytes that escaped age-related muscle atrophy and retained the proliferative response to muscle injury characteristic of younger animals. The preservation of muscle architecture and age-independent regenerative capacity through localized mIgf-1 transgene expression suggests clinical strategies for the treatment of age or disease-related muscle frailty.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/GATA2 Transcription Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Gata2 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor I,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Isoforms,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
|
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
1061-4036
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
27
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
195-200
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:11175789-Animals,
pubmed-meshheading:11175789-Cachexia,
pubmed-meshheading:11175789-Cell Aging,
pubmed-meshheading:11175789-DNA-Binding Proteins,
pubmed-meshheading:11175789-GATA2 Transcription Factor,
pubmed-meshheading:11175789-Hypertrophy,
pubmed-meshheading:11175789-Insulin-Like Growth Factor I,
pubmed-meshheading:11175789-Mice,
pubmed-meshheading:11175789-Mice, Transgenic,
pubmed-meshheading:11175789-Muscle, Skeletal,
pubmed-meshheading:11175789-Neurodegenerative Diseases,
pubmed-meshheading:11175789-Organ Size,
pubmed-meshheading:11175789-Protein Isoforms,
pubmed-meshheading:11175789-Regeneration,
pubmed-meshheading:11175789-Tissue Distribution,
pubmed-meshheading:11175789-Transcription Factors
|
pubmed:year |
2001
|
pubmed:articleTitle |
Localized Igf-1 transgene expression sustains hypertrophy and regeneration in senescent skeletal muscle.
|
pubmed:affiliation |
Cardiovascular Research Center, Massachusetts General Hospital-East, Charlestown, Massachusetts, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
|