| Literature DB >> 32585118 |
D Zhang1, S Zhang1,2, J Wang1,3, Q Li1, H Xue1, R Sheng1, Q Xiong1, X Qi1, J Wen1, Y Fan1, B O Zhou4, Q Yuan1,2.
Abstract
Stem cells play a critical role in bone regeneration. Multiple populations of skeletal stem cells have been identified in long bone, while their identity and functions in alveolar bone remain unclear. Here, we identified a quiescent leptin receptor-expressing (LepR+) cell population that contributed to intramembranous bone formation. Interestingly, these LepR+ cells became activated in response to tooth extraction and generated the majority of the newly formed bone in extraction sockets. In addition, genetic ablation of LepR+ cells attenuated extraction socket healing. The parabiosis experiments revealed that the LepR+ cells in the healing sockets were derived from resident tissue rather than peripheral blood circulation. Further studies on the mechanism suggested that these LepR+ cells were responsive to parathyroid hormone/parathyroid hormone 1 receptor (PTH/PTH1R) signaling. Collectively, we demonstrate that LepR+ cells, a postnatal skeletal stem cell population, are essential for alveolar bone regeneration of extraction sockets.Entities:
Keywords: PTH-PTHrP receptor; cell lineage; leptin receptor; osteogenesis; stem cells; tooth extraction
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Year: 2020 PMID: 32585118 DOI: 10.1177/0022034520932834
Source DB: PubMed Journal: J Dent Res ISSN: 0022-0345 Impact factor: 6.116