Distinct skeletal stem cell types orchestrate long bone skeletogenesis

Author:

Ambrosi Thomas H1ORCID,Sinha Rahul1,Steininger Holly M1,Hoover Malachia Y1,Murphy Matthew P1,Koepke Lauren S1,Wang Yuting1,Lu Wan-Jin1,Morri Maurizio2,Neff Norma F2,Weissman Irving L13,Longaker Michael T145,Chan Charles KF14ORCID

Affiliation:

1. Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, United States

2. Chan Zuckerberg BioHub, San Francisco, United States

3. Ludwig Center for Cancer Stem Cell Biology and Medicine at Stanford University, Stanford, United States

4. Department of Surgery, Stanford University School of Medicine, Stanford, United States

5. Hagey Laboratory for Pediatric Regenerative Medicine, Stanford University School of Medicine, Stanford University, Stanford, United States

Abstract

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.

Funder

Deutsche Forschungsgemeinschaft

National Institute on Aging

Prostate Cancer Foundation

Siebel Foundation

NIDDK

Heritage Medical Foundation

American Federation for Aging Research

Endowment from the DiGenova Family

National Institutes of Health

California Institute of Regenerative Medicine

Oak Foundation

Hagey Laboratory

Pitch Johnson Foundation

Gunn/Olivier Research Fund

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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