4.8 Article

Distinct skeletal stem cell types orchestrate long bone skeletogenesis

Journal

ELIFE
Volume 10, Issue -, Pages -

Publisher

ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.66063

Keywords

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Categories

Funding

  1. Deutsche Forschungsgemeinschaft [399915929]
  2. National Institute on Aging [1K99AG066963, K99-R00AG049958-01A1]
  3. Prostate Cancer Foundation
  4. Siebel Foundation
  5. NIDDK [R01DK115600]
  6. Heritage Medical Foundation
  7. American Federation for Aging Research
  8. DiGenova Family
  9. National Institutes of Health [R56 DE025597, R01 DE026730, R01 DE021683, R21DE024230, DE027323, U01 HL099776, U24 DE026914, R21 DE019274]
  10. California Institute of Regenerative Medicine [CIRMTR1-01249]
  11. Oak Foundation
  12. Hagey Laboratory
  13. Pitch Johnson Foundation
  14. Gunn/Olivier Research Fund

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This research identifies at least two types of bone progenitors in postnatal mouse long bones. One type facilitates bone growth and repair, while the other contributes to shaping the hematopoietic stem cell niche and meeting regenerative demands. The study also reveals that the latter is the origin of bone marrow adipose tissue.
Skeletal stem and progenitor cell populations are crucial for bone physiology. Characterization of these cell types remains restricted to heterogenous bulk populations with limited information on whether they are unique or overlap with previously characterized cell types. Here we show, through comprehensive functional and single-cell transcriptomic analyses, that postnatal long bones of mice contain at least two types of bone progenitors with bona fide skeletal stem cell (SSC) characteristics. An early osteochondral SSC (ocSSC) facilitates long bone growth and repair, while a second type, a perivascular SSC (pvSSC), co-emerges with long bone marrow and contributes to shape the hematopoietic stem cell niche and regenerative demand. We establish that pvSSCs, but not ocSSCs, are the origin of bone marrow adipose tissue. Lastly, we also provide insight into residual SSC heterogeneity as well as potential crosstalk between the two spatially distinct cell populations. These findings comprehensively address previously unappreciated shortcomings of SSC research.

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