Single-cell transcriptomics identifies PDGFRA(+) progenitors orchestrating angiogenesis and periodontal tissue regeneration.

单细胞转录组学鉴定出 PDGFRA(+) 祖细胞,这些祖细胞调控血管生成和牙周组织再生

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作者:Liu Jianing, He Junxi, Zhang Ziqi, Liu Lu, Cao Yuan, Zhang Xiaohui, Cai Xinyue, Luo Xinyan, Lei Xiao, Zhang Nan, Wang Hao, Chen Ji, Liu Peisheng, Tian Jiongyi, Liu Jiexi, Gao Yuru, Xu Haokun, Ma Chao, Bai Shengfeng, Zhang Yubohan, Jin Yan, Zheng Chenxi, Sui Bingdong, Jin Fang
Periodontal bone defects, primarily caused by periodontitis, are highly prevalent in clinical settings and manifest as bone fenestration, dehiscence, or attachment loss, presenting a significant challenge to oral health. In regenerative medicine, harnessing developmental principles for tissue repair offers promising therapeutic potential. Of particular interest is the condensation of progenitor cells, an essential event in organogenesis that has inspired clinically effective cell aggregation approaches in dental regeneration. However, the precise cellular coordination mechanisms during condensation and regeneration remain elusive. Here, taking the tooth as a model organ, we employed single-cell RNA sequencing to dissect the cellular composition and heterogeneity of human dental follicle and dental papilla, revealing a distinct Platelet-derived growth factor receptor alpha (PDGFRA) mesenchymal stem/stromal cell (MSC) population with remarkable odontogenic potential. Interestingly, a reciprocal paracrine interaction between PDGFRA(+) dental follicle stem cells (DFSCs) and CD31(+) Endomucin(+) endothelial cells (ECs) was mediated by Vascular endothelial growth factor A (VEGFA) and Platelet-derived growth factor subunit BB (PDGFBB). This crosstalk not only maintains the functionality of PDGFRA(+) DFSCs but also drives specialized angiogenesis. In vivo periodontal bone regeneration experiments further reveal that communication between PDGFRA(+) DFSC aggregates and recipient ECs is essential for effective angiogenic-osteogenic coupling and rapid tissue repair. Collectively, our results unravel the importance of MSC-EC crosstalk mediated by the VEGFA and PDGFBB-PDGFRA reciprocal signaling in orchestrating angiogenesis and osteogenesis. These findings not only establish a framework for deciphering and promoting periodontal bone regeneration in potential clinical applications but also offer insights for future therapeutic strategies in dental or broader regenerative medicine.

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