Identification of the metaphyseal skeletal stem cell building trabecular bone
Guan Yang, Qi He, Xiaoxiao Guo, Rongyu Li, Jingting Lin, Yiming Lang, Wanyu Tao, Wenjia Liu, Huisang Lin, Shilai Xing, Yini Qi, Zhongliang Xie, Jing‐Dong J. Han, Bin Zhou, Yan Teng, Xiao Yang
Abstract
Skeletal stem cells (SSCs) that are capable of self-renewal and multipotent differentiation contribute to bone development and homeostasis. Several populations of SSCs at different skeletal sites have been reported. Here, we identify a metaphyseal SSC (mpSSC) population whose transcriptional landscape is distinct from other bone mesenchymal stromal cells (BMSCs). These mpSSCs are marked by Sstr2 or Pdgfrb + Kitl − , located just underneath the growth plate, and exclusively derived from hypertrophic chondrocytes (HCs). These HC-derived mpSSCs have properties of self-renewal and multipotency in vitro and in vivo, producing most HC offspring postnatally. HC-specific deletion of Hgs, a component of the endosomal sorting complex required for transport, impairs the HC-to-mpSSC conversion and compromises trabecular bone formation. Thus, mpSSC is the major source of BMSCs and osteoblasts in bone marrow, supporting the postnatal trabecular bone formation.