|  Help  |  About  |  Contact Us

Publication : ERRγ is not required for skeletal development but is a RUNX2-dependent negative regulator of postnatal bone formation in male mice.

First Author  Cardelli M Year  2014
Journal  PLoS One Volume  9
Issue  10 Pages  e109592
PubMed ID  25313644 Mgi Jnum  J:223448
Mgi Id  MGI:5649168 Doi  10.1371/journal.pone.0109592
Citation  Cardelli M, et al. (2014) ERRgamma is not required for skeletal development but is a RUNX2-dependent negative regulator of postnatal bone formation in male mice. PLoS One 9(10):e109592
abstractText  To assess the effects of the orphan nuclear Estrogen receptor-related receptor gamma (ERRgamma) deficiency on skeletal development and bone turnover, we utilized an ERRgamma global knockout mouse line. While we observed no gross morphological anomalies or difference in skeletal length in newborn mice, by 8 weeks of age ERRgamma +/- males but not females exhibited increased trabecular bone, which was further increased by 14 weeks. The increase in trabecular bone was due to an increase in active osteoblasts on the bone surface, without detectable alterations in osteoclast number or activity. Consistent with the histomorphometric results, we observed an increase in gene expression of the bone formation markers alkaline phosphatase (Alp) and bone sialoprotein (Bsp) in bone and increase in serum ALP, but no change in the osteoclast regulators receptor activator of NF-kappaB ligand (RANKL) and osteoprotegerin (OPG) or the resorption marker carboxy-terminal collagen crosslinks (CTX). More colony forming units-alkaline phosphatase and -osteoblast (CFU-ALP, CFU-O respectively) but not CFU-fibroblast (CFU-F) formed in ERRgamma +/- versus ERRgamma +/+ stromal cell cultures, suggesting that ERRgamma negatively regulates osteoblast differentiation and matrix mineralization but not mesenchymal precursor number. By co-immunoprecipitation experiments, we found that ERRgamma and RUNX2 interact in an ERRgamma DNA binding domain (DBD)-dependent manner. Treatment of post-confluent differentiating bone marrow stromal cell cultures with Runx2 antisense oligonucleotides resulted in a reduction of CFU-ALP/CFU-O in ERRgamma +/- but not ERRgamma +/+ mice compared to their corresponding sense controls. Our data indicate that ERRgamma is not required for skeletal development but is a sex-dependent negative regulator of postnatal bone formation, acting in a RUNX2- and apparently differentiation stage-dependent manner.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

2 Authors

4 Bio Entities

Trail: Publication

0 Expression