The orphan nuclear estrogen receptor-related receptor α (ERRα) is expressed throughout osteoblast differentiation and regulates bone formation in vitro
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Bonnelye, E
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Univ Toronto, Fac Med, Dept Anat & Cell Biol, Toronto, ON M5S 1A8, CanadaUniv Toronto, Fac Med, Dept Anat & Cell Biol, Toronto, ON M5S 1A8, Canada
Bonnelye, E
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Merdad, L
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Univ Toronto, Fac Med, Dept Anat & Cell Biol, Toronto, ON M5S 1A8, CanadaUniv Toronto, Fac Med, Dept Anat & Cell Biol, Toronto, ON M5S 1A8, Canada
Merdad, L
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Kung, V
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Univ Toronto, Fac Med, Dept Anat & Cell Biol, Toronto, ON M5S 1A8, CanadaUniv Toronto, Fac Med, Dept Anat & Cell Biol, Toronto, ON M5S 1A8, Canada
Kung, V
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Aubin, JE
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Univ Toronto, Fac Med, Dept Anat & Cell Biol, Toronto, ON M5S 1A8, CanadaUniv Toronto, Fac Med, Dept Anat & Cell Biol, Toronto, ON M5S 1A8, Canada
Aubin, JE
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[1] Univ Toronto, Fac Med, Dept Anat & Cell Biol, Toronto, ON M5S 1A8, Canada
The orphan nuclear estrogen receptor-related receptor alpha (ERR alpha), is expressed by many cell types, but is very highly expressed by osteoblastic cells in which it transactivates at least one osteoblast-associated gene, osteopontin. To study the putative involvement of ERR alpha in bone, we first assessed its expression in rat calvaria (RC) in vivo and in RC cells in vitro. ERR alpha mRNA and protein were expressed at all developmental stages from early osteoprogenitors to bone-forming osteoblasts, but protein was most abundant in mature cuboidal osteoblasts. To assess a functional role for ERR alpha in osteoblast differentiation and bone formation, we blocked its expression by antisense oligonucleotides in either proliferating or differentiating RC cell cultures and found inhibition of cell growth and a proliferation-independent inhibition of differentiation. On the other hand, ERR alpha overexpression in RC cells increased differentiation and maturation of progenitors to mature bone-forming cells. Our findings show that ERR alpha is highly expressed throughout the osteoblast developmental sequence and plays a physiological role in differentiation and bone formation at both proliferation and differentiation stages. In addition, we found that manipulation of receptor levels in the absence of known ligand is a fruitful approach for functional analysis of this orphan receptor and identification of potential target genes.