Circulating Osteoprogenitor Cells Have a Mixed Immune and Mesenchymal Progenitor Function in Humans

Author:

Feehan Jack123,Jacques Macsue3,Kondrikov Dmitry4,Eynon Nir35ORCID,Wijeratne Tissa23,Apostolopoulos Vasso23ORCID,Gimble Jeffrey M6,Hill William D47,Duque Gustavo12389ORCID

Affiliation:

1. Department of Medicine - Western Health, The University of Melbourne , Melbourne, Victoria (VIC) , Australia

2. Australian Institute for Musculoskeletal Science (AIMSS), Western Health, Victoria University and University of Melbourne , Melbourne, Victoria (VIC) , Australia

3. Institute for Health and Sport, Victoria University , Melbourne, Victoria (VIC) , Australia

4. Department of Pathology and Laboratory Medicine, The Medical University of South Carolina , Charleston, SC , USA

5. Australian Regenerative Medicine Institute, Monash University , Clayton, Victoria , Australia

6. Center for Stem Cell Research and Regenerative Medicine, Tulane University School of Medicine , New Orleans, LA , USA

7. Department of Veterans Affairs, Ralph H Johnson VA Medical Center , Charleston, SC , USA

8. Bone, Muscle and Geroscience Research Group, Research Institute of the McGill University Health Centre , Montreal, Quebec , Canada

9. Dr. Joseph Kaufmann Chair in Geriatric Medicine, Department of Medicine, McGill University , Montreal, Quebec , Canada

Abstract

Abstract Background Circulating osteoprogenitors (COP) are a population of cells in the peripheral circulation that possess functional and phenotypical characteristics of multipotent stromal cells (MSCs). This population has a solid potential to become an abundant, accessible, and replenishable source of MSCs with multiple potential clinical applications. However, a comprehensive functional characterization of COP cells is still required to test and fully develop their use in clinical settings. Methods This study characterized COP cells by comparing them to bone marrow-derived MSCs (BM-MSCs) and adipose-derived MSCs (ASCs) through detailed transcriptomic and proteomic analyses. Results We demonstrate that COP cells have a distinct gene and protein expression pattern with a significantly stronger immune footprint, likely owing to their hematopoietic lineage. In addition, regarding progenitor cell differentiation and proliferation pathways, COP cells have a similar expression pattern to BM-MSCs and ASCs. Conclusion COP cells are a unique but functionally similar population to BM-MSCs and ASCs, sharing their proliferation and differentiation capacity, thus presenting an accessible source of MSCs with strong potential for translational regenerative medicine strategies.

Funder

Australian Government Research Training Program Scholarship

Australian Institute for Musculoskeletal Science

National Institutes of Health

National Institute on Aging

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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