» Articles » PMID: 30658653

Extracellular Vesicles in Bone: "dogrobbers" in the "eternal Battle Field"

Overview
Publisher Biomed Central
Date 2019 Jan 20
PMID 30658653
Citations 23
Authors
Affiliations
Soon will be listed here.
Abstract

Throughout human life, bone is constantly in a delicate dynamic equilibrium of synthesis and resorption, hosting finely-tuned bone mineral metabolic processes for bone homeostasis by collaboration or symphony among several cell types including osteoclasts (OCs), osteoblasts (OBs), osteocytes (OYs), vascular endothelial cells (ECs) and their precursors. Beyond these connections, a substantial level of communication seems to occur between bone and other tissues, and together, they form an organic unit linked to human health and disease. However, the current hypothesis, which includes growth factors, hormones and specific protein secretion, incompletely explains the close connections among bone cells or between bone and other tissues. Extracellular vesicles (EVs) are widely-distributed membrane structures consisting of lipid bilayers, membrane proteins and intravesicular cargo (including proteins and nucleic acids), ranging from 30 nm to 1000 nm in diameter, and their characters have been highly conserved throughout evolution. EVs have targeting abilities and the potential to transmit multidimensional, abundant and complicated information, as powerful and substantial "dogrobbers" mediating intercellular communications. As research has progressed, EVs have gradually become thought of as "dogrobbers" in bone tissue-the "eternal battle field" -in a delicate dynamic balance of destruction and reconstruction. In the current review, we give a brief description of the major constituent cells in bone tissues and explore the progress of current research on bone-derived EVs. In addition, this review also discusses in depth not only potential directions for future research to breakthrough in this area but also problems existing in current research that need to be solved for a better understanding of bone tissues.

Citing Articles

Exosomes: intriguing mediators of intercellular communication in the organism's response to noxious agents.

Vucemilovic A Arh Hig Rada Toksikol. 2024; 75(4):228-239.

PMID: 39718095 PMC: 11667715. DOI: 10.2478/aiht-2024-75-3923.


Engineered mammalian and bacterial extracellular vesicles as promising nanocarriers for targeted therapy.

Liu H, Geng Z, Su J Extracell Vesicles Circ Nucl Acids. 2024; 3(2):63-86.

PMID: 39698442 PMC: 11648430. DOI: 10.20517/evcna.2022.04.


Effect of nHA/CS/PLGA delivering adipose stem cell-derived exosomes and bone marrow stem cells on bone healing-in vitro and in vivo studies.

Wang T, Guo S, Zhang Y Sci Rep. 2024; 14(1):27502.

PMID: 39528545 PMC: 11555374. DOI: 10.1038/s41598-024-76672-8.


Effect of primary osteoblast-derived extracellular vesicles on osteoclast differentiation.

Zhang L, Tan J Zhejiang Da Xue Xue Bao Yi Xue Ban. 2024; 53(4):434-442.

PMID: 39034117 PMC: 11375487. DOI: 10.3724/zdxbyxb-2024-0148.


Bioengineering extracellular vesicles: smart nanomaterials for bone regeneration.

Man K, Eisenstein N, Hoey D, Cox S J Nanobiotechnology. 2023; 21(1):137.

PMID: 37106449 PMC: 10134574. DOI: 10.1186/s12951-023-01895-2.


References
1.
Weilner S, Keider V, Winter M, Harreither E, Salzer B, Weiss F . Vesicular Galectin-3 levels decrease with donor age and contribute to the reduced osteo-inductive potential of human plasma derived extracellular vesicles. Aging (Albany NY). 2016; 8(1):16-33. PMC: 4761711. DOI: 10.18632/aging.100865. View

2.
Delgado-Calle J, Tu X, Pacheco-Costa R, McAndrews K, Edwards R, Pellegrini G . Control of Bone Anabolism in Response to Mechanical Loading and PTH by Distinct Mechanisms Downstream of the PTH Receptor. J Bone Miner Res. 2016; 32(3):522-535. PMC: 8502039. DOI: 10.1002/jbmr.3011. View

3.
McCarthy T, Centrella M, Canalis E . Parathyroid hormone enhances the transcript and polypeptide levels of insulin-like growth factor I in osteoblast-enriched cultures from fetal rat bone. Endocrinology. 1989; 124(3):1247-53. DOI: 10.1210/endo-124-3-1247. View

4.
Tao S, Rui B, Wang Q, Zhou D, Zhang Y, Guo S . Extracellular vesicle-mimetic nanovesicles transport LncRNA-H19 as competing endogenous RNA for the treatment of diabetic wounds. Drug Deliv. 2018; 25(1):241-255. PMC: 6058500. DOI: 10.1080/10717544.2018.1425774. View

5.
Tao S, Guo S . Extracellular Vesicles: Potential Participants in Circadian Rhythm Synchronization. Int J Biol Sci. 2018; 14(12):1610-1620. PMC: 6216034. DOI: 10.7150/ijbs.26518. View