Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
1994-9-2
pubmed:abstractText
Temporal and spatial distribution of a gene encoding murine bone morphogenetic protein 4 (mBMP-4) during fracture repair were investigated in mice by RT-PCR and in situ hybridization. For in situ hybridization, fractured ribs and surrounding tissues were decalcified and hybridized with a mBMP-4-specific complementary RNA probe labeled with digoxigenin-11 UTP. mBMP-4 messenger RNA (mRNA) was not detected in ribs without fracture, whereas it was detected only in the early phase of fracture from 12 to 72 h after the onset of fracture before new cartilage or bone formation. The mBMP-4 mRNAs were present in cells distributed in three distinct regions, namely, the proliferating periosteum, the medullary cavity, and the muscles near the fracture site. These BMP-4-positive cells did not express bone gla protein mRNA, which is a marker of the mature osteogenic cell. RT-PCR also showed a transient increase in the level of BMP-4 mRNA in the early phase of fracture repair. The findings provide us with some new information. (1) The BMP-4 gene is produced by less differentiated osteoprogenitor cells, not by differentiated osteoblasts. (2) The BMP-4 gene is enhanced by the impact of fracture and localized in callus-forming tissue before callus formation. Together with the activities of BMP-4, as was previously described, our results suggest that newly produced BMP-4 gene product is one of the local contributing factors in callus formation in the early phase of fracture healing.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0884-0431
pubmed:author
pubmed:issnType
Print
pubmed:volume
9
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
651-9
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:8053394-Animals, pubmed-meshheading:8053394-Base Sequence, pubmed-meshheading:8053394-Blotting, Southern, pubmed-meshheading:8053394-Bone Morphogenetic Proteins, pubmed-meshheading:8053394-Cell Differentiation, pubmed-meshheading:8053394-Deoxyuracil Nucleotides, pubmed-meshheading:8053394-Digoxigenin, pubmed-meshheading:8053394-Fibroblasts, pubmed-meshheading:8053394-Fracture Healing, pubmed-meshheading:8053394-Growth Substances, pubmed-meshheading:8053394-In Situ Hybridization, pubmed-meshheading:8053394-Male, pubmed-meshheading:8053394-Mice, pubmed-meshheading:8053394-Mice, Inbred ICR, pubmed-meshheading:8053394-Molecular Sequence Data, pubmed-meshheading:8053394-Osteoblasts, pubmed-meshheading:8053394-Polymerase Chain Reaction, pubmed-meshheading:8053394-Protein Biosynthesis, pubmed-meshheading:8053394-Proteins, pubmed-meshheading:8053394-RNA, Messenger, pubmed-meshheading:8053394-Rib Fractures, pubmed-meshheading:8053394-Stem Cells
pubmed:year
1994
pubmed:articleTitle
Transient and localized expression of bone morphogenetic protein 4 messenger RNA during fracture healing.
pubmed:affiliation
Department of Orthopaedic Surgery, Osaka University Medical School, Suita, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't