Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2000-3-31
pubmed:abstractText
Multipotential mesenchymal stem cells capable of chondro-osseous induction contribute to the endochondral callus of healing fractured bone. Microvascular pericytes serving the role of multipotential mesenchymal stem cells are considered osteoprogenitors because they express type I collagen, alkaline phosphatase enzyme activity, osteocalcin immunoreactivity, and bone sialoprotein mRNA. Previous electron microscopic studies indicate that this cell type has a contribution to the fracture callus. Limited data suggest that pericytes may also assume a chondrogenic phenotype. We undertook in vitro studies to understand how the chondro-osseous phenotype of the pericyte might be regulated. Using Northern analysis and semiquantitative reverse transcriptase-polymerase chain reaction (RT-PCR), we found that cultured pericytes produce aggrecan and type II collagen mRNA indicating their chondrogenic potential. Aggrecan message is elevated by BMP-2 as analyzed by both Northern hybridization and RT-PCR. This finding suggests a regulatory role for this morphogen on this phenotype in pericytes. RT-PCR amplified versican product was also associated with pericyte cultures but was not affected by BMP-2. Our data strongly support a chondrogenic role for the pericyte and that the phenotype is regulated at least in part by BMP.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Aggrecans, http://linkedlifedata.com/resource/pubmed/chemical/Bone Morphogenetic Protein 2, http://linkedlifedata.com/resource/pubmed/chemical/Bone Morphogenetic Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Chondroitin Sulfate Proteoglycans, http://linkedlifedata.com/resource/pubmed/chemical/Collagen, http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers, http://linkedlifedata.com/resource/pubmed/chemical/Extracellular Matrix Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Lectins, C-Type, http://linkedlifedata.com/resource/pubmed/chemical/Proteoglycans, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta, http://linkedlifedata.com/resource/pubmed/chemical/Versicans
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
0006-291X
pubmed:author
pubmed:copyrightInfo
Copyright 2000 Academic Press.
pubmed:issnType
Print
pubmed:day
5
pubmed:volume
269
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
172-8
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed-meshheading:10694496-Aggrecans, pubmed-meshheading:10694496-Animals, pubmed-meshheading:10694496-Base Sequence, pubmed-meshheading:10694496-Bone Morphogenetic Protein 2, pubmed-meshheading:10694496-Bone Morphogenetic Proteins, pubmed-meshheading:10694496-Cattle, pubmed-meshheading:10694496-Cells, Cultured, pubmed-meshheading:10694496-Chondrogenesis, pubmed-meshheading:10694496-Chondroitin Sulfate Proteoglycans, pubmed-meshheading:10694496-Collagen, pubmed-meshheading:10694496-DNA Primers, pubmed-meshheading:10694496-Extracellular Matrix Proteins, pubmed-meshheading:10694496-Fracture Healing, pubmed-meshheading:10694496-Gene Expression, pubmed-meshheading:10694496-Lectins, C-Type, pubmed-meshheading:10694496-Microcirculation, pubmed-meshheading:10694496-Pericytes, pubmed-meshheading:10694496-Phenotype, pubmed-meshheading:10694496-Proteoglycans, pubmed-meshheading:10694496-RNA, Messenger, pubmed-meshheading:10694496-Recombinant Proteins, pubmed-meshheading:10694496-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:10694496-Transforming Growth Factor beta, pubmed-meshheading:10694496-Versicans
pubmed:year
2000
pubmed:articleTitle
Microvascular pericytes express aggrecan message which is regulated by BMP-2.
pubmed:affiliation
McKay Laboratories for Orthopaedic Surgery Research, Department of Orthopaedic Surgery, School of Medicine, University of Pennsylvania, 36th and Hamilton Walk, Philadelphia, Pennsylvania 19104-6081, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.