Yu Fanyuan, Li Feifei, Yu Peng, Zhou Bin, Ye Ling
State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China; Department of Endodontics, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
State Key Laboratory of Oral Diseases & National Clinical Research Center for Oral Diseases, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Cell Rep. 2022 Nov 8;41(6):111599. doi: 10.1016/j.celrep.2022.111599.
Skeletal stem cells (SSCs) fuel adult bone with stemness resources to maintain homeostasis and support regeneration, which depends on the precise determination of the osteogenic lineage commitment of SSCs. In this study, using Cre-loxP reporter lineage tracking, we identified and characterized a population of NFATc1 SSCs in bone regeneration. Pre-existing NFATc1 SSCs are involved in early bone callus formation. Subsequently, these NFATc1 SSCs produce osteolineage descendants in the subsequent stages of regeneration. The Ca-triggered transcriptional activity of NFATc1 constitutes the pre-imprinted memory of the trajectory to intrinsically orchestrate osteogenesis of SSCs. Inhibition of Ca/NFATc1 signaling in SSCs directly impairs osteogenesis and bone regeneration. In summary, our findings provide a mechanistic understanding of adult bone regeneration through the regulation of NFATc1 SSCs.
骨骼干细胞(SSCs)为成年骨骼提供干性资源,以维持体内平衡并支持再生,这依赖于对SSCs成骨谱系定向的精确确定。在本研究中,我们使用Cre-loxP报告基因谱系追踪技术,在骨再生过程中鉴定并表征了一群NFATc1阳性的骨骼干细胞。已有的NFATc1阳性骨骼干细胞参与早期骨痂形成。随后,这些NFATc1阳性骨骼干细胞在再生的后续阶段产生成骨谱系后代。钙离子触发的NFATc1转录活性构成了内在协调SSCs成骨轨迹的预印记记忆。抑制SSCs中的钙/NFATc1信号直接损害成骨和骨再生。总之,我们的研究结果通过对NFATc1阳性骨骼干细胞的调控,为成年骨再生提供了机制上的理解。