FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2000
Best5: a novel interferon-inducible gene expressed during bone formation.
СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Grewal T S, Genever P G, Brabbs A C, Birch M, Skerry T M
Аннотация
Regulation of bone formation is important in the pathogenesis of many conditions such as osteoporosis, fracture healing, and loosening of orthopedic implants. We have recently identified a novel rat cDNA (best5) by differential display PCR that is regulated during osteoblast differentiation and bone formation in vitro and in vivo. Expression of best5 mRNA is induced in cultures of osteoblasts by both interferon-alpha (IFN-alpha) or IFN-gamma. Whereas IFN-alpha induced a rapid, transient induction of best5 expression peaking at 4-6 h poststimulation, IFN-gamma elicited a more prolonged induction of best5 expression, which remained elevated 48 h poststimulation. A polyclonal antibody generated to a peptide derived from the best5 coding region recognized a 27 kDa protein on Western blot analysis of osteoblast lysates. We localized BEST5 protein in osteoblast progenitor cells and mature osteoblasts in sections of rat tibiae and in sections of bones loaded in vivo to induce adaptive bone formation. Best5 may therefore be a fundamental intermediate in the response of osteoblasts to stimuli that modulate proliferation/differentiation, such as interferons or mechanical loading. These findings highlight the close interactions between the immune system and bone cells and may open new therapeutic avenues in modulating bone mass.
Предметные рубрики MeSH
Amino Acid SequenceAnimalsBone DevelopmentBone Marrow CellsBone NeoplasmsBone and BonesCloning, MolecularGene Expression RegulationHumansInterferon Type IInterferon-gammaInterleukin-1Interleukin-6Iron-Sulfur ProteinsMolecular Sequence DataOsteoblastsOsteosarcomaPolymerase Chain ReactionRNA, MessengerRatsRats, WistarRecombinant ProteinsSequence AlignmentSequence Homology, Amino AcidTranscription, GeneticTumor Cells, CulturedViperin Protein