Spatiotemporal interplay between epithelial and mesenchymal cells drives human dentinogenesis

Tooth dentin, secreted by odontoblasts, constitutes most of the tooth structure and provides support and sensory function. However, dentin defects are common and irreparable once they exceed a critical threshold. Human dentin develops from dental papilla (DP) cells under the guidance of the dental epithelium (DE). Here, we present a human tooth development atlas from initiation to erupted stage using single-cell RNA sequencing and spatial transcriptomics, focusing on epithelial-mesenchymal interactions. This atlas reveals that DE orchestrates DP differentiation in a WNT-NOTCH sequential activation model and identifies the key signaling molecules. DLX6-AS1<sup>+</sup> DP cells respond to dental epithelial signals and can be isolated from adult dental pulp stem cells (DPSCs). Notably, DLX6-AS1<sup>+</sup> DPSCs successfully generate tubular dentin in an in vivo disease model of dentin defects. This research provides valuable information on human tooth development and establishes a basis for repairing regenerative dental tissue.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2026-02-14
DOI
https://doi.org/10.1038/s41467-026-69545-3
Citations
1
Primary Topic
dental development and anomalies
Type
article
Field-Weighted Citation Impact
22.24

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Spatiotemporal interplay between epithelial and mesenchymal cells drives human dentinogenesis

Lanrong Luo, Xiaoshan Wu, Xiuge Gu, Jing Sun et al.
1 citations
Nature Communications
dental development and anomalies
22.24
article

Spatiotemporal interplay between epithelial and mesenchymal cells drives human dentinogenesis

Lanrong Luo, Xiaoshan Wu, Xiuge Gu, Jing Sun, Yuanyuan Zhang, Yang Wang, Ran Zhang, Songlin Wang, Chunmei Zhang, Haijing Zhou, Lei Hu, Wei Wei, Zongshan Shen, Lina Hu, Mengjie Han
article en
1 citations

Abstract

Tooth dentin, secreted by odontoblasts, constitutes most of the tooth structure and provides support and sensory function. However, dentin defects are common and irreparable once they exceed a critical threshold. Human dentin develops from dental papilla (DP) cells under the guidance of the dental epithelium (DE). Here, we present a human tooth development atlas from initiation to erupted stage using single-cell RNA sequencing and spatial transcriptomics, focusing on epithelial-mesenchymal interactions. This atlas reveals that DE orchestrates DP differentiation in a WNT-NOTCH sequential activation model and identifies the key signaling molecules. DLX6-AS1<sup>+</sup> DP cells respond to dental epithelial signals and can be isolated from adult dental pulp stem cells (DPSCs). Notably, DLX6-AS1<sup>+</sup> DPSCs successfully generate tubular dentin in an in vivo disease model of dentin defects. This research provides valuable information on human tooth development and establishes a basis for repairing regenerative dental tissue.

Nature CommunicationsVol. 17(1)
Central South University (CN), Sun Yat-sen University (CN), Capital Medical University (CN), Peking University (CN), Southern University of Science and Technology (CN), National Clinical Research Center for Digestive Diseases (CN), National Clinical Research (US), Stomatology Hospital (CN), Beijing Obstetrics and Gynecology Hospital (CN), South University (US)
National Natural Science Foundation of China, Capital Medical University, National Key Research and Development Program of China
Openalex Percentile: Top 1%
dental development and anomalies
22.24
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.