Source:http://linkedlifedata.com/resource/pubmed/id/18439098
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2008-9-18
|
pubmed:abstractText |
Mesenchymal stem cells (MSCs) have already been proved to be multipotent. Our goal was to evaluate the differentiating ability of rat MSCs into insulin-secreting cells in vitro to cure diabetes resulting from abnormal function of pancreatic islets. MSCs were identified by Fluorescence-activated cell sorting (FACS). Pdx1 is a transcription factor involved in the early endocrine development. Betacellulin (BTC) is a growth factor involved in beta-cell maturation. MSCs were transfected with plasmids carrying rat Pdx1 and BTC genes. Coexpression of Pdx1 and BTC significantly increased the number of nestin-positive epithelium-like progenitors and islet-like spheroids which differentiated from MSCs. In Pdx1- and BTC-expressed (Pdx1+ + BTC+) MSCs, insulin and Glut-2 mRNA levels significantly rose. The number of islet-like cells was also evidently augmented. In response to glucose, Pdx1+ + BTC+ MSCs released insulin and C-peptide. It is concluded that genetic manipulation of transcription factor Pdx1 and growth factor BTC in combination with appropriate differentiating culture could induce MSCs into the pancreatic lineage in vitro and produce islet-like spheroids that could secrete increased levels of insulin in response to glucose.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Homeodomain Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Signaling Peptides...,
http://linkedlifedata.com/resource/pubmed/chemical/Intermediate Filament Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Nerve Tissue Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators,
http://linkedlifedata.com/resource/pubmed/chemical/betacellulin,
http://linkedlifedata.com/resource/pubmed/chemical/nestin,
http://linkedlifedata.com/resource/pubmed/chemical/pancreatic and duodenal homeobox 1...
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
1557-8534
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
17
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
815-23
|
pubmed:dateRevised |
2011-6-1
|
pubmed:meshHeading |
pubmed-meshheading:18439098-Animals,
pubmed-meshheading:18439098-Cell Differentiation,
pubmed-meshheading:18439098-Cells, Cultured,
pubmed-meshheading:18439098-Epithelium,
pubmed-meshheading:18439098-Gene Expression,
pubmed-meshheading:18439098-Homeodomain Proteins,
pubmed-meshheading:18439098-Insulin-Secreting Cells,
pubmed-meshheading:18439098-Intercellular Signaling Peptides and Proteins,
pubmed-meshheading:18439098-Intermediate Filament Proteins,
pubmed-meshheading:18439098-Mesenchymal Stem Cells,
pubmed-meshheading:18439098-Nerve Tissue Proteins,
pubmed-meshheading:18439098-Rats,
pubmed-meshheading:18439098-Rats, Sprague-Dawley,
pubmed-meshheading:18439098-Spheroids, Cellular,
pubmed-meshheading:18439098-Trans-Activators
|
pubmed:year |
2008
|
pubmed:articleTitle |
Coexpression of Pdx1 and betacellulin in mesenchymal stem cells could promote the differentiation of nestin-positive epithelium-like progenitors and pancreatic islet-like spheroids.
|
pubmed:affiliation |
College of Life Sciences, Peking University, Beijing, People's Republic of China.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|