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Requirement of Pdgfrα+ cells for calvarial bone repair.
Xing, Xin; Li, Zhao; Xu, Jiajia; Chen, Austin Z; Archer, Mary; Wang, Yiyun; Xu, Mingxin; Wang, Ziyi; Zhu, Manyu; Qin, Qizhi; Thottappillil, Neelima; Zhou, Myles; James, Aaron W.
Affiliation
  • Xing X; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Li Z; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Xu J; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Chen AZ; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Archer M; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Wang Y; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Xu M; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Wang Z; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Zhu M; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Qin Q; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Thottappillil N; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • Zhou M; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
  • James AW; Department of Pathology, Johns Hopkins University, Baltimore, MD 21205, United States.
Article in En | MEDLINE | ID: mdl-38986535
ABSTRACT
Platelet-derived growth factor receptor α (PDGFRα) is often considered as a general marker of mesenchymal cells and fibroblasts, but also shows expression in a portion of osteoprogenitor cells. Within the skeleton, Pdgfrα+ mesenchymal cells have been identified in bone marrow and periosteum of long bones, where they play a crucial role in participating in fracture repair. A similar examination of Pdgfrα+ cells in calvarial bone healing has not been examined. Here, we utilize Pdgfrα-CreERTM;mT/mG reporter animals to examine the contribution of Pdgfrα+ mesenchymal cells to calvarial bone repair through histology and single-cell RNA sequencing (scRNA-Seq). Results showed that Pdgfrα+ mesenchymal cells are present in several cell clusters by scRNA-Seq, and by histology a dramatic increase in Pdgfrα+ cells populated the defect site at early timepoints to give rise to healed bone tissue overtime. Notably, diphtheria toxin-mediated ablation of Pdgfrα reporter+ cells resulted in significantly impaired calvarial bone healing. Our findings suggest that Pdgfrα-expressing cells within the calvarial niche play a critical role in the process of calvarial bone repair.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Stem Cells Transl Med Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Stem Cells Transl Med Year: 2024 Document type: Article Affiliation country:
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