Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Dec 7:10:1091360.
doi: 10.3389/fbioe.2022.1091360. eCollection 2022.

Engineering exosomes for bone defect repair

Affiliations
Review

Engineering exosomes for bone defect repair

Shaoyang Ma et al. Front Bioeng Biotechnol. .

Abstract

Currently, bone defect repair is still an intractable clinical problem. Numerous treatments have been performed, but their clinical results are unsatisfactory. As a key element of cell-free therapy, exosome is becoming a promising tool of bone regeneration in recent decades, because of its promoting osteogenesis and osteogenic differentiation function in vivo and in vitro. However, low yield, weak activity, inefficient targeting ability, and unpredictable side effects of natural exosomes have limited the clinical application. To overcome the weakness, various approaches have been applied to produce engineering exosomes by regulating their production and function at present. In this review, we will focus on the engineering exosomes for bone defect repair. By summarizing the exosomal cargos affecting osteogenesis, the strategies of engineering exosomes and properties of exosome-integrated biomaterials, this work will provide novel insights into exploring advanced engineering exosome-based cell-free therapy for bone defect repair.

Keywords: bone regeneration; engineering exosomes; exosomal cargos; exosome-integrated biomaterials; osteogenesis.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Schematic of exosomal cargos (miRNA, lncRNA, circRNA, tsRNA, mRNA and protein) with the function of promoting bone regeneration.
FIGURE 2
FIGURE 2
Three strategies of engineering exosomes for bone regeneration. ODM: osteogenic differentiation medium.
FIGURE 3
FIGURE 3
The properties of biomaterial (hydrogel and metal scaffold) help exosomes to promote bone regeneration.

Similar articles

Cited by

References

    1. Alvarez-Erviti L., Seow Y., Yin H., Betts C., Lakhal S., Wood M. J. (2011). Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes. Nat. Biotechnol. 29, 341–345. [PubMed: 341]. 10.1038/nbt.1807 - DOI - PubMed
    1. Ando Y., Matsubara K., Ishikawa J., Fujio M., Shohara R., Hibi H., et al. (2014). Stem cell-conditioned medium accelerates distraction osteogenesis through multiple regenerative mechanisms. Bone 61, 82–90. [PubMed: 82]. 10.1016/j.bone.2013.12.029 - DOI - PubMed
    1. Bahar D., Gonen Z. B., Gumusderelioglu M., Onger M. E., Tokak E. K., Ozturk-Kup F., et al. (2022). Repair of rat calvarial bone defect by using exosomes of umbilical cord-derived mesenchymal stromal cells embedded in chitosan/hydroxyapatite scaffolds. Int. J. Oral Maxillofac. Implants 37, 943–950. [PubMed: 943]. 10.11607/jomi.9515 - DOI - PubMed
    1. Balatti V., Nigita G., Veneziano D., Drusco A., Stein G. S., Messier T. L., et al. (2017). tsRNA signatures in cancer. Proc. Natl. Acad. Sci. U. S. A. 114, 8071–8076. [PubMed: 28696308]. 10.1073/pnas.1706908114 - DOI - PMC - PubMed
    1. Behera J., Kumar A., Voor M. J., Tyagi N. (2021). Exosomal lncRNA-H19 promotes osteogenesis and angiogenesis through mediating Angpt1/Tie2-NO signaling in CBS-heterozygous mice. Theranostics 11, 7715–7734. [PubMed: 34335960]. 10.7150/thno.58410 - DOI - PMC - PubMed