Isaac J, Erthal J, Gordon J, Duverger O, Sun H-W, Lichtler A C, Stein G S, Lian J B, Morasso M I
Laboratory of Skin Biology, NIAMS, NIH, Bethesda, MD, USA.
Department of Biochemistry, University of Vermont, Burlington, VT, USA.
Cell Death Differ. 2014 Sep;21(9):1365-76. doi: 10.1038/cdd.2014.82. Epub 2014 Jun 20.
Human mutations and in vitro studies indicate that DLX3 has a crucial function in bone development, however, the in vivo role of DLX3 in endochondral ossification has not been established. Here, we identify DLX3 as a central attenuator of adult bone mass in the appendicular skeleton. Dynamic bone formation, histologic and micro-computed tomography analyses demonstrate that in vivo DLX3 conditional loss of function in mesenchymal cells (Prx1-Cre) and osteoblasts (OCN-Cre) results in increased bone mass accrual observed as early as 2 weeks that remains elevated throughout the lifespan owing to increased osteoblast activity and increased expression of bone matrix genes. Dlx3OCN-conditional knockout mice have more trabeculae that extend deeper in the medullary cavity and thicker cortical bone with an increased mineral apposition rate, decreased bone mineral density and increased cortical porosity. Trabecular TRAP staining and site-specific Q-PCR demonstrated that osteoclastic resorption remained normal on trabecular bone, whereas cortical bone exhibited altered osteoclast patterning on the periosteal surface associated with high Opg/Rankl ratios. Using RNA sequencing and chromatin immunoprecipitation-Seq analyses, we demonstrate that DLX3 regulates transcription factors crucial for bone formation such as Dlx5, Dlx6, Runx2 and Sp7 as well as genes important to mineral deposition (Ibsp, Enpp1, Mepe) and bone turnover (Opg). Furthermore, with the removal of DLX3, we observe increased occupancy of DLX5, as well as increased and earlier occupancy of RUNX2 on the bone-specific osteocalcin promoter. Together, these findings provide novel insight into mechanisms by which DLX3 attenuates bone mass accrual to support bone homeostasis by osteogenic gene pathway regulation.
人类突变和体外研究表明,DLX3在骨骼发育中具有关键作用,然而,DLX3在软骨内成骨中的体内作用尚未明确。在此,我们确定DLX3是附属骨骼中成人骨量的核心衰减因子。动态骨形成、组织学和显微计算机断层扫描分析表明,间充质细胞(Prx1-Cre)和成骨细胞(OCN-Cre)中DLX3的体内条件性功能丧失导致骨量增加,最早在2周时即可观察到,由于成骨细胞活性增加和骨基质基因表达增加,这种增加在整个生命周期中持续存在。Dlx3OCN条件性敲除小鼠有更多的小梁,这些小梁在髓腔内延伸更深,皮质骨更厚,矿物质沉积率增加,骨矿物质密度降低,皮质孔隙率增加。小梁TRAP染色和位点特异性Q-PCR表明,小梁骨上的破骨细胞吸收保持正常,而皮质骨在骨膜表面表现出与高Opg/Rankl比率相关的破骨细胞模式改变。使用RNA测序和染色质免疫沉淀测序分析,我们证明DLX3调节对骨形成至关重要的转录因子,如Dlx5、Dlx6、Runx2和Sp7,以及对矿物质沉积(Ibsp、Enpp1、Mepe)和骨转换(Opg)重要的基因。此外,随着DLX3的去除,我们观察到DLX5的占有率增加,以及RUNX2在骨特异性骨钙素启动子上的占有率增加且更早。总之,这些发现为DLX3通过调节成骨基因途径来衰减骨量积累以支持骨稳态的机制提供了新的见解。