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Departments of Research and Medicine, Saint Francis Hospital and Medical Center, Hartford 06105; and The University of Connecticut School of Medicine, Farmington, Connecticut 06030
Leukemia inhibitory
factor (LIF) and oncostatin M (OSM) have multiple effects on skeletal
remodeling. Although these cytokines modestly regulate collagen
synthesis in osteoblasts, their effects on collagenase expression and
collagen degradation are not known. We tested whether LIF and OSM
regulate the expression of matrix metalloproteinases (MMPs) and tissue
inhibitors of metalloproteinases (TIMPs) in osteoblast-enriched cells
isolated from fetal rat calvariae. LIF and OSM increased collagenase-3
(MMP-13) mRNA and immunoreactive protein levels in a time- and
dose-dependent manner. LIF and OSM enhanced the rate of transcription
of the collagenase gene and stabilized collagenase mRNA in
transcriptionally arrested cells. LIF and OSM failed to regulate the
expression of gelatinase A (MMP-2) and B (MMP-9). LIF and OSM modestly
stimulated the expression of TIMP-1 but did not alter the expression of
TIMP-2 and -3. In conclusion, LIF and OSM stimulate collagenase-3 and
TIMP-1 expression in osteoblasts, and these effects may be involved in
mediating the bone remodeling actions of these cytokines.
cytokines; collagen degradation; matrix metalloproteinases; tissue inhibitors of metalloproteinases; gelatinases
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