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Osteoprotegerin mRNA is increased by interleukin-1 alpha in the human osteosarcoma cell line MG-63 and in human osteoblast-like cells.

Vidal, Olle (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin,Institute of Internal Medicine
Sjögren, Klara, 1970 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för internmedicin,Institute of Internal Medicine, Dept of Medicine
Eriksson, B I (author)
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Ljunggren, O (author)
Ohlsson, Claes, 1965 (author)
Gothenburg University,Göteborgs universitet,Institutionen för invärtesmedicin, Avdelningen för internmedicin,Institute of Internal Medicine, Dept of Medicine
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 (creator_code:org_t)
Elsevier BV, 1998
1998
English.
In: Biochemical and biophysical research communications. - : Elsevier BV. - 0006-291X. ; 248:3, s. 696-700
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Osteoprotegerin (OPG) is a soluble receptor for the Osteoprotegerin-Ligand (OPGL) which is expressed on osteoblasts and mediates the signal for osteoclast differentiation. In the present study we demonstrate that OPG mRNA levels in MG-63 cells are increased in a dose-dependent manner after 8 h of treatment with IL-1 alpha (338 +/- 53% over control at 25 U/ml). Interleukin-6 (IL-6), under similar culture conditions, does not affect OPG mRNA levels. Time-course studies show that IL-1 alpha (25 U/ml) causes a transient increase of OPG mRNA levels in MG-63 cells, peaking after 4 h of treatment. An increase of the OPG transcript occurs in hOB cells at 0.5 h which is still present after 24 h of IL-1 alpha treatment. In MG-63 cells neither basal-nor IL-1 alpha-induced OPG mRNA levels are altered by the translational inhibitor cycloheximide. These results suggest that expression of OPG in osteoblasts may be regulated by IL-1 alpha.

Keyword

Bone Neoplasms
Cell Differentiation
Cycloheximide
pharmacology
Dose-Response Relationship
Drug
Gene Expression Regulation
drug effects
Gene Expression Regulation
Neoplastic
drug effects
Glycoproteins
biosynthesis
Humans
Interleukin-1
pharmacology
Kinetics
Osteoblasts
drug effects
metabolism
Osteoclasts
cytology
Osteoprotegerin
Osteosarcoma
Polymerase Chain Reaction
RNA
Messenger
biosynthesis
Receptors
Cytoplasmic and Nuclear
Receptors
Tumor Necrosis Factor
biosynthesis
Signal Transduction
Transcription
Genetic
drug effects
Tumor Cells
Cultured

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