Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
18
pubmed:dateCreated
2006-5-3
pubmed:abstractText
Chemically defined medium (CDM) conditions for controlling human embryonic stem cell (hESC) fate will not only facilitate the practical application of hESCs in research and therapy but also provide an excellent system for studying the molecular mechanisms underlying self-renewal and differentiation, without the multiple unknown and variable factors associated with feeder cells and serum. Here we report a simple CDM that supports efficient self-renewal of hESCs grown on a Matrigel-coated surface over multiple passages. Expanded hESCs under such conditions maintain expression of multiple hESC-specific markers, retain the characteristic hESC morphology, possess a normal karyotype in vitro, as well as develop teratomas in vivo. Additionally, several growth factors were found to selectively induce monolayer differentiation of hESC cultures toward neural, definitive endoderm/pancreatic and early cardiac muscle cells, respectively, in our CDM conditions. Therefore, this CDM condition provides a basic platform for further characterization of hESC self-renewal and directed differentiation, as well as the development of novel therapies.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-10047466, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-10748519, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-11489934, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-11581665, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-11716562, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-11731781, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-12242268, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-12426580, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-12524553, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-12724518, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-12791707, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-14636556, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-1511725, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-15310843, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-15501227, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-15579640, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-15782187, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-15790770, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-15809086, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-15905405, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-16002783, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-16179608, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-16258519, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-16388305, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-6217835, http://linkedlifedata.com/resource/pubmed/commentcorrection/16632596-9804556
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0027-8424
pubmed:author
pubmed:issnType
Print
pubmed:day
2
pubmed:volume
103
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6907-12
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:16632596-Activins, pubmed-meshheading:16632596-Animals, pubmed-meshheading:16632596-Biological Markers, pubmed-meshheading:16632596-Bone Morphogenetic Proteins, pubmed-meshheading:16632596-Carrier Proteins, pubmed-meshheading:16632596-Cell Culture Techniques, pubmed-meshheading:16632596-Cell Differentiation, pubmed-meshheading:16632596-Cell Lineage, pubmed-meshheading:16632596-Cells, Cultured, pubmed-meshheading:16632596-Culture Media, pubmed-meshheading:16632596-Embryo, Mammalian, pubmed-meshheading:16632596-Endoderm, pubmed-meshheading:16632596-Humans, pubmed-meshheading:16632596-Inhibin-beta Subunits, pubmed-meshheading:16632596-Karyotyping, pubmed-meshheading:16632596-Mice, pubmed-meshheading:16632596-Mice, Nude, pubmed-meshheading:16632596-Myocardium, pubmed-meshheading:16632596-Neurons, pubmed-meshheading:16632596-Pancreas, pubmed-meshheading:16632596-Stem Cells
pubmed:year
2006
pubmed:articleTitle
Long-term self-renewal and directed differentiation of human embryonic stem cells in chemically defined conditions.
pubmed:affiliation
Department of Chemistry, The Scripps Research Institute, SR202, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't