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Therapeutic application of extracellular vesicles for musculoskeletal repair & regeneration

  • Khairat Bahgat Youssef El Baradie(corresponding author)
    ,
  • Mark W. Hamrick
*Corresponding author for this work
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

Traumatic musculoskeletal injuries are common in both the civilian and combat care settings. Significant barriers exist to repairing these injuries including fracture nonunion, muscle fibrosis, re-innervation, and compartment syndrome, as well as infection and inflammation. Recently, extracellular vesicles (EVs), including exosomes and microvesicles, have attracted attention in the field of musculoskeletal regeneration. These vesicles are released by different cell types and play a vital role in cell communication by delivering functional cargoes such as proteins and RNAs. Many of these cargo molecules can be utilized for repair purposes in skeletal disorders such as osteoporosis, osteogenesis imperfecta, sarcopenia, and fracture healing. There are, however, some challenges to overcome in order to advance the successful application of these vesicles in the therapeutic setting. These include large-scale production and isolation of exosomes, long-term storage, in vivo stability, and strategies for tissue-specific targeting and delivery. This paper reviews the general characteristics of exosomes along with their physiological roles and contribution to the pathogenesis of musculoskeletal diseases. We also highlight new findings on the use of synthetic exosomes to overcome the limitations of native exosomes in treating musculoskeletal injuries and disorders.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 99-114 (16 pages)

Journal (Volume, Issue Number)

Connective Tissue Research (Volume 62, Issue 1)

Publication milestones

  • Accepted/In press - 2020
  • Published - 2021

Publication status

Published - 2021

ISSN

0300-8207

Publication IDs

  • Scopus: 85087526083
  • PubMed: 32602385

Publication metrics

Metrics

SciVal
citations
1
SciVal
FWCI
3.11
SciVal
Author count
2
SciVal
Paper percentile
92
SciVal
Top percentile
10
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
0.50
Fractional count
1
Fractional count
1
Scopus
citations

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Citation count
16
Captures
35

Funding Details

This work was supported by the US Army Medical Research and Materiel Command CDMRP Program Grant [DM160252] and the US National Institute of Aging [AG036675].
FundersFunding numbers
US National Institute of Aging
AG036675
MRMC
DM160252