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标记的牙髓祖细胞是小鼠磨牙出生后成牙本质细胞和牙髓细胞的主要贡献者。

-labeled pulp progenitor cells are main contributors to postnatal odontoblasts and pulp cells in murine molars.

作者信息

Yang Dongwook, Jeong YoungJae, Ortinau Laura, Solidum Jea, Park Dongsu

出版信息

bioRxiv. 2024 Mar 27:2024.03.21.586156. doi: 10.1101/2024.03.21.586156.

Abstract

Regeneration of dentin and odontoblasts from dental pulp stem cells (DPSCs) is essential for permanent tooth maintenance. However, the identity and role of endogenous DPSCs in reparative dentinogenesis are elusive. Here, using pulp single-cell analysis before and after molar eruption, we revealed that endogenous DPSCs are enriched in GFP coronal papilla-like cells with Cre labeling. These GFP cells are long-term repopulating cells that contribute to the majority of pulp cells and new odontoblasts after eruption. Upon molar injury, DPSCs localize into the injury site and differentiate into new odontoblasts, forming -GFP and -GFP dentinal tubules and reparative dentin. Single-cell and FACS analysis showed that GFP DPSCs are the most primitive cells with stem cell marker expression and odontoblast differentiation. Taken together, our findings demonstrate that labels postnatal DSPCs, which are the main source of pulp cells and new odontoblasts with reparative dentinogenesis .

摘要

牙髓干细胞(DPSCs)再生牙本质和成牙本质细胞对于恒牙维持至关重要。然而,内源性DPSCs在修复性牙本质形成中的身份和作用尚不清楚。在这里,通过对磨牙萌出前后的牙髓进行单细胞分析,我们发现内源性DPSCs在具有Cre标记的GFP冠状乳头样细胞中富集。这些GFP细胞是长期再填充细胞,在萌出后对大多数牙髓细胞和新的成牙本质细胞有贡献。磨牙损伤后,DPSCs定位于损伤部位并分化为新的成牙本质细胞,形成GFP和GFP牙本质小管以及修复性牙本质。单细胞和FACS分析表明,GFP DPSCs是具有干细胞标志物表达和成牙本质细胞分化的最原始细胞。综上所述,我们的研究结果表明,标记出生后的DSPCs,它们是牙髓细胞和具有修复性牙本质形成的新成牙本质细胞的主要来源。

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