Mx1标记的牙髓祖细胞是小鼠磨牙中牙本质细胞和成牙本质再生的主要贡献者。

Mx1-labeled pulp progenitor cells are the main contributors of odontoblast and dentin regeneration in murine molars.

作者信息

Yang Dongwook, Jeong Youngjae, Ortinau Laura, Solidum Jea Giezl, Park Dongsu

机构信息

Department of Molecular Human Genetics, Baylor College of Medicine, Houston, TX, USA.

Department of Biochemistry and Molecular Biology, College of Medicine, University of the Philippines, Manila, Philippines.

出版信息

Exp Mol Med. 2025 Aug 13. doi: 10.1038/s12276-025-01511-3.

Abstract

Regeneration of dentin and odontoblasts from dental pulp progenitor cells is essential for the maintenance of permanent tooth. However, the in vivo identity of endogenous pulp progenitor cells and how they contribute to reparative dentinogenesis remain elusive. Here we show that comparative single-cell analysis of pulp cells before and after molar eruption reveal that endogenous pulp progenitor cells are enriched in coronal papilla-like cells with Mx1-Cre and Cxcl12-GFP expression. Further, lineage tracing and fluorescence-activated cell sorting analysis indicated that Mx1-labeled (Mx1) pulp cells include long-term repopulating progenitor cells with higher expression of stem cell markers. Notably, these Mx1 progenitor cells contribute to the majority of pulp cells and new odontoblast-like cells in the loaded plane of the molar after eruption. Upon molar injury, Mx1 progenitor cells localize into the injury site and differentiate into new odontoblast-like cells, forming osteocalcin-GFP and scleraxis-GFP processes to reoccupy existing dentinal tubules and reparative dentin formation. Taken together, our findings demonstrate that Mx1 labels dental pulp progenitor cells, which are the major source of pulp cells and odontoblast-like cells with reparative dentinogenesis in vivo.

摘要

牙髓祖细胞再生牙本质和成牙本质细胞对于恒牙的维持至关重要。然而,内源性牙髓祖细胞在体内的特性以及它们如何促进修复性牙本质形成仍不清楚。在这里,我们表明,对磨牙萌出前后的牙髓细胞进行比较单细胞分析发现,内源性牙髓祖细胞在具有Mx1-Cre和Cxcl12-GFP表达的冠状乳头样细胞中富集。此外,谱系追踪和荧光激活细胞分选分析表明,Mx1标记的(Mx1)牙髓细胞包括具有更高干细胞标志物表达的长期再填充祖细胞。值得注意的是,这些Mx1祖细胞在磨牙萌出后的加载平面中构成了大多数牙髓细胞和新的成牙本质细胞样细胞。磨牙损伤后,Mx1祖细胞定位于损伤部位并分化为新的成牙本质细胞样细胞,形成骨钙素-GFP和硬骨素-GFP突起,重新占据现有的牙本质小管并形成修复性牙本质。综上所述,我们的研究结果表明,Mx1标记牙髓祖细胞,它们是体内牙髓细胞和成牙本质细胞样细胞的主要来源,并具有修复性牙本质形成能力。

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