Core Laboratory for Phenomics and Diagnostic, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Department of Medical Research, Kaohsiung Chang Gung Memorial Hospital, Kaohsiung, Taiwan.
Cell Death Dis. 2019 Sep 23;10(10):705. doi: 10.1038/s41419-019-1942-1.
Osteoporosis deteriorates bone mass and biomechanical strength, becoming a life-threatening cause to the elderly. MicroRNA is known to regulate tissue remodeling; however, its role in the development of osteoporosis remains elusive. In this study, we uncovered that silencing miR-29a expression decreased mineralized matrix production in osteogenic cells, whereas osteoclast differentiation and pit formation were upregulated in bone marrow macrophages as co-incubated with the osteogenic cells in transwell plates. In vivo, decreased miR-29a expression occurred in ovariectomy-mediated osteoporotic skeletons. Mice overexpressing miR-29a in osteoblasts driven by osteocalcin promoter (miR-29aTg/OCN) displayed higher bone mineral density, trabecular volume and mineral acquisition than wild-type mice. The estrogen deficiency-induced loss of bone mass, trabecular morphometry, mechanical properties, mineral accretion and osteogenesis of bone marrow mesenchymal cells were compromised in miR-29aTg/OCN mice. miR-29a overexpression also attenuated the estrogen loss-mediated excessive osteoclast surface histopathology, osteoclast formation of bone marrow macrophages, receptor activator nuclear factor-κ ligand (RANKL) and C-X-C motif chemokine ligand 12 (CXCL12) expression. Treatment with miR-29a precursor improved the ovariectomy-mediated skeletal deterioration and biomechanical property loss. Mechanistically, miR-29a inhibited RANKL secretion in osteoblasts through binding to 3'-UTR of RANKL. It also suppressed the histone acetyltransferase PCAF-mediated acetylation of lysine 27 in histone 3 (H3K27ac) and decreased the H3K27ac enrichment in CXCL12 promoters. Taken together, miR-29a signaling in osteogenic cells protects bone tissue from osteoporosis through repressing osteoclast regulators RANKL and CXCL12 to reduce osteoclastogenic differentiation. Arrays of analyses shed new light on the miR-29a regulation of crosstalk between osteogenic and osteoclastogenic cells. We also highlight that increasing miR-29a function in osteoblasts is beneficial for bone anabolism to fend off estrogen deficiency-induced excessive osteoclastic resorption and osteoporosis.
骨质疏松症会导致骨量和生物力学强度恶化,成为老年人的生命威胁。已知 microRNA 可调节组织重塑;然而,其在骨质疏松症发展中的作用仍不清楚。在这项研究中,我们发现沉默 miR-29a 的表达会降低成骨细胞中矿化基质的产生,而在与成骨细胞共培养的骨髓巨噬细胞中,破骨细胞分化和陷窝形成被上调。在体内,卵巢切除介导的骨质疏松骨骼中发生了 miR-29a 表达的降低。在骨钙素启动子驱动的成骨细胞中过表达 miR-29a(miR-29aTg/OCN)的小鼠比野生型小鼠具有更高的骨矿物质密度、小梁体积和矿物质获取量。在 miR-29aTg/OCN 小鼠中,雌激素缺乏引起的骨量、小梁形态、机械性能、矿物质沉积和骨髓间充质细胞成骨的损失得到了补偿。miR-29a 的过表达也减弱了雌激素缺失介导的破骨细胞表面组织病理学、骨髓巨噬细胞的破骨细胞形成、核因子κB 受体激活剂配体 (RANKL) 和 C-X-C 基序趋化因子配体 12 (CXCL12) 的表达。用 miR-29a 前体治疗改善了卵巢切除介导的骨骼恶化和生物力学性能丧失。从机制上讲,miR-29a 通过与 RANKL 的 3'-UTR 结合抑制 RANKL 在成骨细胞中的分泌。它还抑制了组蛋白乙酰转移酶 PCAF 介导的组蛋白 3 (H3) 赖氨酸 27 乙酰化 (H3K27ac),并减少了 CXCL12 启动子中 H3K27ac 的富集。总之,成骨细胞中的 miR-29a 信号通过抑制破骨细胞调节因子 RANKL 和 CXCL12 来减少破骨细胞生成,从而保护骨组织免受骨质疏松症的影响。一系列分析为 miR-29a 调节成骨细胞和破骨细胞之间的细胞间通讯提供了新的视角。我们还强调,增加成骨细胞中的 miR-29a 功能有利于骨合成,以抵御雌激素缺乏引起的过度破骨细胞吸收和骨质疏松症。