Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
22
pubmed:dateCreated
2005-5-30
pubmed:abstractText
Mutations in the Wnt co-receptor LRP5 alter bone mass in humans, but the mechanisms responsible for Wnts actions in bone are unclear. To investigate the role of the classical Wnt signaling pathway in osteogenesis, we generated mice lacking the beta-catenin or adenomatous polyposis coli (Apc) genes in osteoblasts. Loss of beta-catenin produced severe osteopenia with striking increases in osteoclasts, whereas constitutive activation of beta-catenin in the conditional Apc mutants resulted in dramatically increased bone deposition and a disappearance of osteoclasts. In vitro, osteoblasts lacking the beta-catenin gene exhibited impaired maturation and mineralization with elevated expression of the osteoclast differentiation factor, receptor activated by nuclear factor-kappaB ligand (RANKL), and diminished expression of the RANKL decoy receptor, osteoprotegerin. By contrast, Apc-deficient osteoblasts matured normally but demonstrated decreased expression of RANKL and increased osteoprotegerin. These findings suggest that Wnt/beta-catenin signaling in osteoblasts coordinates postnatal bone acquisition by controlling the differentiation and activity of both osteoblasts and osteoclasts.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Adenomatous Polyposis Coli Protein, http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Catnb protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Cytoskeletal Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Green Fluorescent Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Signaling Peptides..., http://linkedlifedata.com/resource/pubmed/chemical/Membrane Glycoproteins, http://linkedlifedata.com/resource/pubmed/chemical/Osteoprotegerin, http://linkedlifedata.com/resource/pubmed/chemical/RANK Ligand, http://linkedlifedata.com/resource/pubmed/chemical/Receptor Activator of Nuclear..., http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cytoplasmic and Nuclear, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tumor Necrosis Factor, http://linkedlifedata.com/resource/pubmed/chemical/Tnfrsf11a protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Tnfrsf11b protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Tnfsf11 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Wnt Proteins, http://linkedlifedata.com/resource/pubmed/chemical/beta Catenin
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
3
pubmed:volume
280
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
21162-8
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:15802266-Adenomatous Polyposis Coli Protein, pubmed-meshheading:15802266-Animals, pubmed-meshheading:15802266-Animals, Newborn, pubmed-meshheading:15802266-Bone Diseases, Metabolic, pubmed-meshheading:15802266-Bone and Bones, pubmed-meshheading:15802266-Carrier Proteins, pubmed-meshheading:15802266-Cell Differentiation, pubmed-meshheading:15802266-Cytoskeletal Proteins, pubmed-meshheading:15802266-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:15802266-Female, pubmed-meshheading:15802266-Femur, pubmed-meshheading:15802266-Gene Expression Regulation, pubmed-meshheading:15802266-Genes, APC, pubmed-meshheading:15802266-Genotype, pubmed-meshheading:15802266-Glycoproteins, pubmed-meshheading:15802266-Green Fluorescent Proteins, pubmed-meshheading:15802266-Immunohistochemistry, pubmed-meshheading:15802266-Intercellular Signaling Peptides and Proteins, pubmed-meshheading:15802266-Male, pubmed-meshheading:15802266-Membrane Glycoproteins, pubmed-meshheading:15802266-Mice, pubmed-meshheading:15802266-Mice, Transgenic, pubmed-meshheading:15802266-Mutation, pubmed-meshheading:15802266-Osteoblasts, pubmed-meshheading:15802266-Osteoclasts, pubmed-meshheading:15802266-Osteoprotegerin, pubmed-meshheading:15802266-RANK Ligand, pubmed-meshheading:15802266-Receptor Activator of Nuclear Factor-kappa B, pubmed-meshheading:15802266-Receptors, Cytoplasmic and Nuclear, pubmed-meshheading:15802266-Receptors, Tumor Necrosis Factor, pubmed-meshheading:15802266-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:15802266-Sex Factors, pubmed-meshheading:15802266-Signal Transduction, pubmed-meshheading:15802266-Time Factors, pubmed-meshheading:15802266-Tomography, X-Ray Computed, pubmed-meshheading:15802266-Trans-Activators, pubmed-meshheading:15802266-Wnt Proteins, pubmed-meshheading:15802266-beta Catenin
pubmed:year
2005
pubmed:articleTitle
Essential role of beta-catenin in postnatal bone acquisition.
pubmed:affiliation
Laboratory of Cell Signaling and Carcinogenesis, Van Andel Research Institute, Grand Rapids, Michigan 49503, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural