Ce Shan, Wei Wang, Hui Lu, Kun Wang, Tianshu Wang, Ziwei Zhang, Mingxu Li, Yongqiang Chen, Zhi-Xiong Jim Xiao, Haoyang Cai, Weidong Tian, Yunqiu Zhang, Bei Li, Zhonghan Li
{"title":"A spatially organized Cd24a+/Pax9+ stem cell core governs postnatal tooth establishment","authors":"Ce Shan, Wei Wang, Hui Lu, Kun Wang, Tianshu Wang, Ziwei Zhang, Mingxu Li, Yongqiang Chen, Zhi-Xiong Jim Xiao, Haoyang Cai, Weidong Tian, Yunqiu Zhang, Bei Li, Zhonghan Li","doi":"10.1126/sciadv.adu5653","DOIUrl":null,"url":null,"abstract":"<div >Mineralized tissues are fundamental in mechanical support and protection in vertebrates. Their formation by progenitor cells during development remains elusive. Here, we show that the postnatal establishment of the molar teeth was governed by a spatially organized core of <i>Cd24a</i><sup>+</sup>/<i>Pax9</i><sup>+</sup> progenitors that persisted into adulthood. <i>Cd24a</i><sup>+</sup> cells gave rise to the dentin-pulp complex, while <i>Pax9</i><sup>+</sup> ones mainly generated periodontal tissues. During development, guided by alveolar bone–derived PDGFB (platelet-derived growth factor, B polypeptide), <i>Cd24a</i><sup>+</sup>/<i>Pax9</i><sup>+</sup> cells gradually concentrated on the apical region during the crown-to-root transition, collectively migrated and formed dental root. Cell ablation and conditional Wnt knockout notably compromised tooth establishment. Single-cell RNA sequencing, CUT&Tag, and spatial mapping further revealed distinct features of <i>Cd24a</i><sup>+</sup>/<i>Pax9</i><sup>+</sup> cells and their cellular organization. Last, the <i>CD24</i><sup>+</sup>/<i>PAX9</i><sup>+</sup> core was also present in human teeth, suggesting it as a conserved developmental program. Together, our work underscores the role of spatially organized dental stem cells in the postnatal establishment of a model mineralized organ in mammals.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"11 23","pages":""},"PeriodicalIF":11.7000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.adu5653","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.adu5653","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Mineralized tissues are fundamental in mechanical support and protection in vertebrates. Their formation by progenitor cells during development remains elusive. Here, we show that the postnatal establishment of the molar teeth was governed by a spatially organized core of Cd24a+/Pax9+ progenitors that persisted into adulthood. Cd24a+ cells gave rise to the dentin-pulp complex, while Pax9+ ones mainly generated periodontal tissues. During development, guided by alveolar bone–derived PDGFB (platelet-derived growth factor, B polypeptide), Cd24a+/Pax9+ cells gradually concentrated on the apical region during the crown-to-root transition, collectively migrated and formed dental root. Cell ablation and conditional Wnt knockout notably compromised tooth establishment. Single-cell RNA sequencing, CUT&Tag, and spatial mapping further revealed distinct features of Cd24a+/Pax9+ cells and their cellular organization. Last, the CD24+/PAX9+ core was also present in human teeth, suggesting it as a conserved developmental program. Together, our work underscores the role of spatially organized dental stem cells in the postnatal establishment of a model mineralized organ in mammals.
期刊介绍:
Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.