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The Role of Bone-Derived Exosomes in Regulating Skeletal Metabolism and Extraosseous Diseases

Overview
Specialty Cell Biology
Date 2020 Apr 8
PMID 32258024
Citations 23
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Abstract

Bone-derived exosomes are naturally existing nano-sized extracellular vesicles secreted by various cells, such as bone marrow stromal cells, osteoclasts, osteoblasts, and osteocytes, containing multifarious proteins, lipids, and nucleic acids. Accumulating evidence indicates that bone-derived exosomes are involved in the regulation of skeletal metabolism and extraosseous diseases through modulating intercellular communication and the transfer of materials. Following the development of research, we found that exosomes can be considered as a potential candidate as a drug delivery carrier thanks to its ability to transport molecules into targeted cells with high stability, safety, and efficiency. This review aims to discuss the emerging role of bone-derived exosomes in skeletal metabolism and extraosseous diseases as well as their potential role as candidate biomarkers or for developing new therapeutic strategies.

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References
1.
Kubota K, Nakano M, Kobayashi E, Mizue Y, Chikenji T, Otani M . An enriched environment prevents diabetes-induced cognitive impairment in rats by enhancing exosomal miR-146a secretion from endogenous bone marrow-derived mesenchymal stem cells. PLoS One. 2018; 13(9):e0204252. PMC: 6150479. DOI: 10.1371/journal.pone.0204252. View

2.
Zhao C, Irie N, Takada Y, Shimoda K, Miyamoto T, Nishiwaki T . Bidirectional ephrinB2-EphB4 signaling controls bone homeostasis. Cell Metab. 2006; 4(2):111-21. DOI: 10.1016/j.cmet.2006.05.012. View

3.
Nevius E, Pinho F, Dhodapkar M, Jin H, Nadrah K, Horowitz M . Oxysterols and EBI2 promote osteoclast precursor migration to bone surfaces and regulate bone mass homeostasis. J Exp Med. 2015; 212(11):1931-46. PMC: 4612084. DOI: 10.1084/jem.20150088. View

4.
Moerman E, Teng K, Lipschitz D, Lecka-Czernik B . Aging activates adipogenic and suppresses osteogenic programs in mesenchymal marrow stroma/stem cells: the role of PPAR-gamma2 transcription factor and TGF-beta/BMP signaling pathways. Aging Cell. 2004; 3(6):379-89. PMC: 1850101. DOI: 10.1111/j.1474-9728.2004.00127.x. View

5.
Zhao C, Sun W, Zhang P, Ling S, Li Y, Zhao D . miR-214 promotes osteoclastogenesis by targeting Pten/PI3k/Akt pathway. RNA Biol. 2015; 12(3):343-53. PMC: 4615895. DOI: 10.1080/15476286.2015.1017205. View