Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2010-4-1
pubmed:abstractText
We investigated the ability of fetal mesenchymal stem cells (fMSCs) to differentiate into brown and white adipocytes and compared the expression of a number of marker genes and key regulatory factors. We showed that the expression of key adipocyte regulators and markers during differentiation is similar to that in other human and murine adipocyte models, including induction of PPARgamma2 and FABP4. Notably, we found that the preadipocyte marker, Pref-1, is induced early in differentiation and then declines markedly as the process continues, suggesting that fMSCs first acquire preadipocyte characteristics as they commit to the adipogenic lineage, prior to their differentiation into mature adipocytes. After adipogenic induction, some stem cell isolates differentiated into cells resembling brown adipocytes and others into white adipocytes. Detailed investigation of one isolate showed that the novel brown fat-determining factor PRDM16 is expressed both before and after differentiation. Importantly, these cells exhibited elevated basal UCP-1 expression, which was dependent on the activity of the orphan nuclear receptor ERRalpha, highlighting a novel role for ERRalpha in human brown fat. Thus fMSCs represent a useful in vitro model for human adipogenesis, and provide opportunities to study the stages prior to commitment to the adipocyte lineage. They also offer invaluable insights into the characteristics of human brown fat.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DLK1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/ERRalpha estrogen-related receptor, http://linkedlifedata.com/resource/pubmed/chemical/FABP4 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Fatty Acid-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/Ion Channels, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Mitochondrial Proteins, http://linkedlifedata.com/resource/pubmed/chemical/PPAR gamma, http://linkedlifedata.com/resource/pubmed/chemical/PRDM16 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Estrogen, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, http://linkedlifedata.com/resource/pubmed/chemical/mitochondrial uncoupling protein
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1748-7838
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
20
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
434-44
pubmed:dateRevised
2010-10-6
pubmed:meshHeading
pubmed-meshheading:20101261-Adipocytes, Brown, pubmed-meshheading:20101261-Adipocytes, White, pubmed-meshheading:20101261-Animals, pubmed-meshheading:20101261-Cell Differentiation, pubmed-meshheading:20101261-DNA-Binding Proteins, pubmed-meshheading:20101261-Fatty Acid-Binding Proteins, pubmed-meshheading:20101261-Fetus, pubmed-meshheading:20101261-Humans, pubmed-meshheading:20101261-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:20101261-Ion Channels, pubmed-meshheading:20101261-Membrane Proteins, pubmed-meshheading:20101261-Mesenchymal Stem Cells, pubmed-meshheading:20101261-Mice, pubmed-meshheading:20101261-Mitochondrial Proteins, pubmed-meshheading:20101261-PPAR gamma, pubmed-meshheading:20101261-Receptors, Estrogen, pubmed-meshheading:20101261-Transcription Factors
pubmed:year
2010
pubmed:articleTitle
Human fetal mesenchymal stem cells differentiate into brown and white adipocytes: a role for ERRalpha in human UCP1 expression.
pubmed:affiliation
Department of Molecular Endocrinology, Institution of Reproductive and Developmental Biology, Imperial College London, London, UK.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't