Single-cell RNA-sequence analysis of human bone marrow reveals new targets for isolation of skeletal stem cells using spherical nucleic acids

Author:

Matthews Elloise Z1ORCID,Lanham Stuart12,White Kate1,Kyriazi Maria-Eleni3,Alexaki Konstantina4ORCID,El-Sagheer Afaf H56,Brown Tom5,Kanaras Antonios G47,J West Jonathan24,MacArthur Ben D178,Stumpf Patrick S19,Oreffo Richard OC1710

Affiliation:

1. Faculty of Medicine, Centre for Human Development, Stem Cells and Regeneration, Human Development and Health, Institute of Developmental Sciences, University of Southampton, Southampton, UK

2. Cancer Sciences, Faculty of Medicine, University of Southampton, Southampton, UK

3. College of Engineering and Technology, American University of the Middle East, Kuwait

4. Physics and Astronomy, Faculty of Physical Sciences and Engineering, University of Southampton, Southampton, UK

5. Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Oxford, UK

6. Chemistry Branch, Department of Science and Mathematics, Faculty of Petroleum and Mining Engineering, Suez University, Suez, Egypt

7. Institute for Life Sciences, University of Southampton, Southampton, UK

8. Mathematical Sciences, University of Southampton, Southampton, UK

9. Joint Research Center for Computational Biomedicine, RWTH Aachen University, Aachen, Germany

10. College of Biomedical Engineering, China Medical University, Taichung, Taiwan

Abstract

There is a wealth of data indicating human bone marrow contains skeletal stem cells (SSC) with the capacity for osteogenic, chondrogenic and adipogenic differentiation. However, current methods to isolate SSCs are restricted by the lack of a defined marker, limiting understanding of SSC fate, immunophenotype, function and clinical application. The current study applied single-cell RNA-sequencing to profile human adult bone marrow populations from 11 donors and identified novel targets for SSC enrichment. Spherical nucleic acids were used to detect these mRNA targets in SSCs. This methodology was able to rapidly isolate potential SSCs found at a frequency of <1 in 1,000,000 in human bone marrow, with the capacity for tri-lineage differentiation in vitro and ectopic bone formation in vivo. The current studies detail the development of a platform to advance SSC enrichment from human bone marrow, offering an invaluable resource for further SSC characterisation, with significant therapeutic impact therein.

Publisher

SAGE Publications

Subject

Biomedical Engineering,Biomaterials,Medicine (miscellaneous)

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