Human skeletal development and regeneration are shaped by functional diversity of stem cells across skeletal sites

The skeleton is one of the most structurally and compositionally diverse organ systems in the human body, depending on unique cellular dynamisms. Here, we integrate prospective isolation of human skeletal stem cells (hSSCs; CD45<sup>-</sup>CD235a<sup>-</sup>TIE2<sup>-</sup>CD31<sup>-</sup>CD146<sup>-</sup>PDPN<sup>+</sup>CD73<sup>+</sup>CD164<sup>+</sup>) from ten skeletal sites with functional assays and single-cell RNA sequencing (scRNA-seq) analysis to identify chondrogenic, osteogenic, stromal, and fibrogenic subtypes of hSSCs during development and their linkage to skeletal phenotypes. We map the distinct composition of hSSC subtypes across multiple skeletal sites and demonstrate their unique in vivo clonal dynamics. We find that age-related changes in bone formation and regeneration disorders stem from a pathological fibroblastic shift in the hSSC pool. Utilizing a Boolean algorithm, we uncover gene regulatory networks that dictate differences in the ability of hSSCs to generate specific skeletal tissues. Importantly, hSSC lineage dynamics are pharmacologically malleable, providing a new strategy to treat aberrant hSSC diversity central to aging and skeletal maladies.

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Publication Details

Journal
Cell stem cell
Published
2025-03-20
DOI
https://doi.org/10.1016/j.stem.2025.02.013
Citations
12
Primary Topic
Mesenchymal stem cell research
Type
article
Field-Weighted Citation Impact
19.50
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article

Human skeletal development and regeneration are shaped by functional diversity of stem cells across skeletal sites

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12 citations
Cell stem cell
Mesenchymal stem cell research
19.50
article

Human skeletal development and regeneration are shaped by functional diversity of stem cells across skeletal sites

George P. Yang, Michael T. Longaker, Daniel Dan Liu, Franco Felix, Maurizio Morri, Rahul Sinha, Malachia Hoover, Stuart B. Goodman, Kelly C. Weldon, Sahar Taheri, Lauren S. Koepke, Jan Sokol, Thomas H. Ambrosi, J. Kent Leach, Wan-Jin Lu, Julius A. Bishop, Holly Steininger, Derrick C. Wan, Michael J. Gardner, Charles K. F. Chan, Augustine M. Saiz, Norma Neff, Stephanie D. Conley, Irving L. Weissman, Eleanor A. Hunt, Noelle L. Van Rysselberghe, L. Henry Goodnough, Erika E. Wheeler, Yuting Wang, Kun Chen, Liming Zhao, Aijun Wang, Yongheng Wang, Debashis Sahoo, Matthew P. Murphy
article en
12 citations

Abstract

The skeleton is one of the most structurally and compositionally diverse organ systems in the human body, depending on unique cellular dynamisms. Here, we integrate prospective isolation of human skeletal stem cells (hSSCs; CD45<sup>-</sup>CD235a<sup>-</sup>TIE2<sup>-</sup>CD31<sup>-</sup>CD146<sup>-</sup>PDPN<sup>+</sup>CD73<sup>+</sup>CD164<sup>+</sup>) from ten skeletal sites with functional assays and single-cell RNA sequencing (scRNA-seq) analysis to identify chondrogenic, osteogenic, stromal, and fibrogenic subtypes of hSSCs during development and their linkage to skeletal phenotypes. We map the distinct composition of hSSC subtypes across multiple skeletal sites and demonstrate their unique in vivo clonal dynamics. We find that age-related changes in bone formation and regeneration disorders stem from a pathological fibroblastic shift in the hSSC pool. Utilizing a Boolean algorithm, we uncover gene regulatory networks that dictate differences in the ability of hSSCs to generate specific skeletal tissues. Importantly, hSSC lineage dynamics are pharmacologically malleable, providing a new strategy to treat aberrant hSSC diversity central to aging and skeletal maladies.

Cell stem cellVol. 32(5)
University of Alabama at Birmingham (US), Chan Zuckerberg Biohub San Francisco (US), Stanford Health Care (US), Chan Zuckerberg Initiative (United States) (US), University of California, Davis (US), Stanford University (US)
Openalex Percentile: Top 1%
Mesenchymal stem cell research
19.50
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