Identification of Salivary Exosome-Derived miRNAs as Potential Biomarkers of Bone Remodeling During Orthodontic Tooth Movement

被引:0
|
作者
Kazanopoulos, Nikolaos [1 ]
Sideris, Constantinos D. [2 ]
Xu, Yong [1 ]
Konstantonis, Dimitrios [3 ]
Vastardis, Heleni [3 ]
Balmayor, Elizabeth R. [4 ]
Wolf, Michael [5 ]
Apel, Christian [1 ]
机构
[1] RWTH Aachen Univ Hosp, Inst Appl Med Engn, Dept Biohybrid & Med Text, D-52074 Aachen, Germany
[2] Natl & Kapodistrian Univ Athens, Dept Biol, Athens 10561, Greece
[3] Natl & Kapodistrian Univ Athens, Sch Dent, Dept Orthodont, Athens 10561, Greece
[4] RWTH Aachen Univ Hosp, Dept Orthopaed Trauma & Reconstruct Surg, Expt Orthopaed & Trauma Surg, D-52074 Aachen, Germany
[5] RWTH Aachen Univ Hosp, Dept Orthodont, D-52074 Aachen, Germany
关键词
extracellular vesicles; osteogenesis; saliva; gene expression regulation; mechanical stress; GINGIVAL CREVICULAR FLUID; OSTEOCLAST DIFFERENTIATION; MECHANICAL-STRESS; OSTEOPROTEGERIN; MECHANOTRANSDUCTION; TRANSCRIPTION; RESORPTION; INTEGRINS; LIGAND; CELL;
D O I
10.3390/ijms26031228
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Orthodontic tooth movement (OTM) is a complex process involving bone remodeling, and is regulated by various molecular factors, including microRNAs (miRNAs). These small, non-coding RNAs are critical in post-transcriptional gene regulation and have been implicated in the modulation of osteoclast and osteoblast activity during OTM. This study aimed to explore the expression profiles of salivary exosome-derived miRNAs during OTM to identify potential biomarkers that could provide insights into the biological processes involved in orthodontic tooth movement. Saliva samples were collected from 15 patients at three time points: before treatment (Day 0), 7 days after the treatment's onset (Day 7), and 40 days after the treatment's onset (Day 40). The exosomes were isolated, and the miRNAs were extracted and sequenced. A differential expression analysis and gene ontology (GO) enrichment were performed to identify the miRNAs involved in osteoblast and osteoclast differentiation. Out of the 1405 detected miRNAs, 185 were analyzed. Several miRNAs were associated with bone-remodeling processes. The statistically significant finding was the downregulation of hsa-miR-4634 after 40 days of treatment. These findings contribute to the understanding of miRNA regulation in orthodontics and may have broader implications for skeletal disorders, such as osteoporosis.
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页数:17
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