Craniofacial bone regeneration remains a major clinical challenge, yet the identity of orofacial mesenchymal stem/stromal cells (OMSCs) has not been fully elucidated. Here, we performed single-cell RNA sequencing (scRNA-seq) on mouse orofacial bone and identified multiple stromal cell clusters. Cell-cell communication mapping and trajectory inference uncovered the heterogeneity of OMSCs and functional divergence among subpopulations. We identified a previously unrecognized population, Smmhc-expressing mesenchymal stem/stromal cells (MSCs), at the earliest stage of the progenitor lineage trajectory. In vivo lineage tracing demonstrated that Smmhc(+) MSCs are multipotent, giving rise to osteoblasts, osteocytes, periodontal ligament (PDL) cells, and dental pulp cells. Targeted ablation of Smmhc(+) MSCs using Smmhc(CreER);iDTR mouse model led to impaired orofacial bone development and disrupted orofacial tissue homeostasis, characterized by reduced osteogenic differentiation and non-cell autonomous reduction of bone resorption. Collectively, this study establishes a cellular atlas of OMSCs and identifies Smmhc(+) MSCs as a functionally indispensable subset for craniofacial bone homeostasis, orchestrating the dynamic balance between osteogenesis and bone resorption within the orofacial skeletal niche.
Identification of Smmhc-expressing mesenchymal cells in orofacial bone at single-cell resolution.
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作者:Fan Yi, Wei Yali, Wu Zhuoxuan, Huang Qin, Cui Chen, Li Zucen, Xu Ruoshi, Yuan Quan, Zhou Chenchen
| 期刊: | Bone Research | 影响因子: | 15.000 |
| 时间: | 2026 | 起止号: | 2026 Mar 23; 14(1):33 |
| doi: | 10.1038/s41413-026-00518-4 | ||
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