» Articles » PMID: 36157529

Application of Exosome-derived Noncoding RNAs in Bone Regeneration: Opportunities and Challenges

Overview
Date 2022 Sep 26
PMID 36157529
Authors
Affiliations
Soon will be listed here.
Abstract

With advances in the fields of regenerative medicine, cell-free therapy has received increased attention. Exosomes have a variety of endogenous properties that provide stability for molecular transport across biological barriers to cells, as a form of cell-to-cell communication that regulates function and phenotype. In addition, exosomes are an important component of paracrine signaling in stem-cell-based therapy and can be used as a stand-alone therapy or as a drug delivery system. The remarkable potential of exosomes has paved the pathway for cell-free treatment in bone regeneration. Exosomes are enriched in distinct noncoding RNAs (ncRNAs), including microRNAs, long ncRNAs and circular RNAs. Different ncRNAs have multiple functions. Altered expression of ncRNA in exosomes is associated with the regenerative potential and development of various diseases, such as femoral head osteonecrosis, myocardial infarction, and cancer. Although there is increasing evidence that exosome-derived ncRNAs (exo-ncRNAs) have the potential for bone regeneration, the detailed mechanisms are not fully understood. Here, we review the biogenesis of exo-ncRNA and the effects of ncRNAs on angiogenesis and osteoblast- and osteoclast-related pathways in different diseases. However, there are still many unsolved problems and challenges in the clinical application of ncRNA; for instance, production, storage, targeted delivery and therapeutic potency assessment. Advancements in exo-ncRNA methods and design will promote the development of therapeutics, revolutionizing the present landscape.

Citing Articles

Adipose-derived stem cell exosomal miR-21-5p enhances angiogenesis in endothelial progenitor cells to promote bone repair via the NOTCH1/DLL4/VEGFA signaling pathway.

Cao L, Sun K, Zeng R, Yang H J Transl Med. 2024; 22(1):1009.

PMID: 39516839 PMC: 11549876. DOI: 10.1186/s12967-024-05806-3.


Exosomal miR-1a-3p derived from glucocorticoid-stimulated M1 macrophages promotes the adipogenic differentiation of BMSCs in glucocorticoid-associated osteonecrosis of the femoral head by targeting Cebpz.

Duan P, Yu Y, Cheng Y, Nie M, Yang Q, Xia L J Nanobiotechnology. 2024; 22(1):648.

PMID: 39438865 PMC: 11494760. DOI: 10.1186/s12951-024-02923-5.


Exosomal non-coding RNAs: Emerging insights into therapeutic potential and mechanisms in bone healing.

Shi H, Yang Y, Xing H, Jia J, Xiong W, Guo S J Tissue Eng. 2024; 15:20417314241286606.

PMID: 39371940 PMC: 11456177. DOI: 10.1177/20417314241286606.


Mechanically strained osteocyte-derived exosomes contained miR-3110-5p and miR-3058-3p and promoted osteoblastic differentiation.

Zhu Y, Li Y, Cao Z, Xue J, Wang X, Hu T Biomed Eng Online. 2024; 23(1):44.

PMID: 38705993 PMC: 11070085. DOI: 10.1186/s12938-024-01237-9.


Regulatory mechanisms of circular RNAs during human mesenchymal stem cell osteogenic differentiation.

Mazziotta C, Badiale G, Cervellera C, Tognon M, Martini F, Rotondo J Theranostics. 2024; 14(1):143-158.

PMID: 38164139 PMC: 10750202. DOI: 10.7150/thno.89066.


References
1.
Percival C, Richtsmeier J . Angiogenesis and intramembranous osteogenesis. Dev Dyn. 2013; 242(8):909-22. PMC: 3803110. DOI: 10.1002/dvdy.23992. View

2.
Martinez-Greene J, Hernandez-Ortega K, Quiroz-Baez R, Resendis-Antonio O, Pichardo-Casas I, Sinclair D . Quantitative proteomic analysis of extracellular vesicle subgroups isolated by an optimized method combining polymer-based precipitation and size exclusion chromatography. J Extracell Vesicles. 2021; 10(6):e12087. PMC: 8077108. DOI: 10.1002/jev2.12087. View

3.
Lv Q, Deng J, Chen Y, Wang Y, Liu B, Liu J . Engineered Human Adipose Stem-Cell-Derived Exosomes Loaded with miR-21-5p to Promote Diabetic Cutaneous Wound Healing. Mol Pharm. 2020; 17(5):1723-1733. DOI: 10.1021/acs.molpharmaceut.0c00177. View

4.
Liu W, Li L, Rong Y, Qian D, Chen J, Zhou Z . Hypoxic mesenchymal stem cell-derived exosomes promote bone fracture healing by the transfer of miR-126. Acta Biomater. 2019; 103:196-212. DOI: 10.1016/j.actbio.2019.12.020. View

5.
Clarke B . Normal bone anatomy and physiology. Clin J Am Soc Nephrol. 2008; 3 Suppl 3:S131-9. PMC: 3152283. DOI: 10.2215/CJN.04151206. View