Human perivascular stem cell-derived extracellular vesicles mediate bone repair

Author:

Xu Jiajia1ORCID,Wang Yiyun1,Hsu Ching-Yun1,Gao Yongxing1,Meyers Carolyn Ann1,Chang Leslie1,Zhang Leititia12,Broderick Kristen3,Ding Catherine4,Peault Bruno456,Witwer Kenneth78,James Aaron Watkins1ORCID

Affiliation:

1. Department of Pathology, Johns Hopkins University, Baltimore, United States

2. Department of Oral and Maxillofacial Surgery, School of Stomatology, China Medical University, Shenyang, China

3. Department of Surgery, Johns Hopkins University, Baltimore, United States

4. Department of Orthopaedic Surgery, Orthopaedic Hospital Research Center, UCLA, Orthopaedic Hospital, Los Angeles, United States

5. Centre For Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom

6. MRC Centre for Regenerative Medicine, University of Edinburgh, Edinburgh, United Kingdom

7. Department of Molecular and Comparative Pathobiology, Johns Hopkins University, Baltimore, United States

8. Department of Neurology, Johns Hopkins University, Baltimore, United States

Abstract

The vascular wall is a source of progenitor cells that are able to induce skeletal repair, primarily by paracrine mechanisms. Here, the paracrine role of extracellular vesicles (EVs) in bone healing was investigated. First, purified human perivascular stem cells (PSCs) were observed to induce mitogenic, pro-migratory, and pro-osteogenic effects on osteoprogenitor cells while in non-contact co-culture via elaboration of EVs. PSC-derived EVs shared mitogenic, pro-migratory, and pro-osteogenic properties of their parent cell. PSC-EV effects were dependent on surface-associated tetraspanins, as demonstrated by EV trypsinization, or neutralizing antibodies for CD9 or CD81. Moreover, shRNA knockdown in recipient cells demonstrated requirement for the CD9/CD81 binding partners IGSF8 and PTGFRN for EV bioactivity. Finally, PSC-EVs stimulated bone repair, and did so via stimulation of skeletal cell proliferation, migration, and osteodifferentiation. In sum, PSC-EVs mediate the same tissue repair effects of perivascular stem cells, and represent an ‘off-the-shelf’ alternative for bone tissue regeneration.

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

National Institute of Dental and Craniofacial Research

Department of Defense

American Cancer Society

Orthopaedic Research and Education Foundation

Maryland Stem Cell Research Fund

Musculoskeletal Transplant Foundation

Publisher

eLife Sciences Publications, Ltd

Subject

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

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