Department of Cell and Developmental Biology, School of Dentistry, Seoul National University, Seoul, 03080, Republic of Korea.
Dental Research Institute, School of Dentistry, Seoul National University, Seoul, 03080, Republic of Korea.
Exp Mol Med. 2024 Aug;56(8):1791-1806. doi: 10.1038/s12276-024-01290-3. Epub 2024 Aug 1.
Bone homeostasis is maintained by an intricate balance between osteoclasts and osteoblasts, which becomes disturbed in osteoporosis. Metallothioneins (MTs) are major contributors in cellular zinc regulation. However, the role of MTs in bone cell regulation has remained unexplored. Single-cell RNA sequencing analysis discovered that, unlike the expression of other MT members, the expression of MT3 was unique to osteoclasts among various macrophage populations and was highly upregulated during osteoclast differentiation. This unique MT3 upregulation was validated experimentally and supported by ATAC sequencing data analyses. Downregulation of MT3 by gene knockdown or knockout resulted in excessive osteoclastogenesis and exacerbated bone loss in ovariectomy-induced osteoporosis. Transcriptome sequencing of MT3 knockdown osteoclasts and gene set enrichment analysis indicated that the oxidative stress and redox pathways were enriched, which was verified by MT3-dependent regulation of reactive oxygen species (ROS). In addition, MT3 deficiency increased the transcriptional activity of SP1 in a manner dependent on intracellular zinc levels. This MT3-zinc-SP1 axis was crucial for the control of osteoclasts, as zinc chelation and SP1 knockdown abrogated the promotion of SP1 activity and osteoclastogenesis by MT3 deletion. Moreover, SP1 bound to the NFATc1 promoter, and overexpression of an inactive SP1 mutant negated the effects of MT3 deletion on NFATc1 and osteoclastogenesis. In conclusion, MT3 plays a pivotal role in controlling osteoclastogenesis and bone metabolism via dual axes involving ROS and SP1. The present study demonstrated that MT3 elevation is a potential therapeutic strategy for osteolytic bone disorders, and it established for the first time that MT3 is a crucial bone mass regulator.
骨稳态是由破骨细胞和成骨细胞之间的复杂平衡维持的,而这种平衡在骨质疏松症中被打乱。金属硫蛋白(MTs)是细胞锌调节的主要贡献者。然而,MTs 在骨细胞调节中的作用仍未被探索。单细胞 RNA 测序分析发现,与其他 MT 成员的表达不同,MT3 的表达在各种巨噬细胞群体中是破骨细胞所特有的,并且在破骨细胞分化过程中高度上调。这种独特的 MT3 上调在实验中得到了验证,并得到了 ATAC 测序数据分析的支持。通过基因敲低或敲除 MT3 导致破骨细胞过度生成和去卵巢诱导的骨质疏松症中骨丢失加剧。MT3 敲低破骨细胞的转录组测序和基因集富集分析表明,氧化应激和氧化还原途径被富集,这通过 MT3 对活性氧(ROS)的依赖性调节得到了验证。此外,MT3 缺乏以依赖细胞内锌水平的方式增加 SP1 的转录活性。MT3-锌-SP1 轴对于破骨细胞的控制至关重要,因为锌螯合和 SP1 敲低消除了 MT3 缺失对 SP1 活性和破骨细胞生成的促进作用。此外,SP1 结合到 NFATc1 启动子上,过表达无活性的 SP1 突变体否定了 MT3 缺失对 NFATc1 和破骨细胞生成的影响。总之,MT3 通过涉及 ROS 和 SP1 的两个轴在控制破骨细胞生成和骨代谢中发挥关键作用。本研究表明,MT3 升高是治疗溶骨性骨疾病的一种潜在治疗策略,并首次确立 MT3 是一种重要的骨量调节剂。