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Single-cell transcriptomic analysis identifies a highly replicating Cd168 skeletal stem/progenitor cell population in mouse long bones. | LitMetric

AI Article Synopsis

  • Skeletal stem/progenitor cells (SSPCs) are found in bones and are essential for bone development, maintenance, and healing, but their diversity and regenerative abilities in mice need more research.
  • This study uses advanced single-cell RNA sequencing to analyze SSPC populations in mouse bones and identifies various cell types involved in bone growth and regeneration.
  • A new population of SSPCs named Cd168 was discovered, which shows strong regenerative potential and is found in specific areas of postnatal mouse bones, indicating its role in healing and tissue formation.

Article Abstract

Skeletal stem/progenitor cells (SSPCs) are tissue-specific stem/progenitor cells localized within skeletons and contribute to bone development, homeostasis, and regeneration. However, the heterogeneity of SSPC populations in mouse long bones and their respective regenerative capacity remain to be further clarified. In this study, we perform integrated analysis using single-cell RNA sequencing (scRNA-seq) datasets of mouse hindlimb buds, postnatal long bones, and fractured long bones. Our analyses reveal the heterogeneity of osteochondrogenic lineage cells and recapitulate the developmental trajectories during mouse long bone growth. In addition, we identify a novel Cd168 SSPC population with highly replicating capacity and osteochondrogenic potential in embryonic and postnatal long bones. Moreover, the Cd168 SSPCs can contribute to newly formed skeletal tissues during fracture healing. Furthermore, the results of multicolor immunofluorescence show that Cd168 SSPCs reside in the superficial zone of articular cartilage as well as in growth plates of postnatal mouse long bones. In summary, we identify a novel Cd168 SSPC population with regenerative potential in mouse long bones, which adds to the knowledge of the tissue-specific stem cells in skeletons.

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Source
http://dx.doi.org/10.1016/j.jgg.2023.04.004DOI Listing

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