Exploring microRNAs in craniofacial regenerative medicine

被引:4
|
作者
Su, Dan [1 ,2 ]
Swearson, Samuel [1 ]
Krongbaramee, Tadkamol [3 ,4 ]
Sun, Hongli [3 ]
Hong, Liu [2 ,3 ]
Amendt, Brad A. [1 ,2 ,3 ]
机构
[1] Univ Iowa, Dept Anat & Cell Biol, Iowa City, IA 52242 USA
[2] Univ Iowa, Craniofacial Anomalies Res Ctr, Iowa City, IA 52242 USA
[3] Univ Iowa, Iowa Inst Oral Hlth Res, Iowa City, IA 52242 USA
[4] Chiang Mai Univ, Fac Dent, Dept Restorat Dent & Periodontol, Div Endodont, Chiang Mai, Thailand
基金
美国国家卫生研究院;
关键词
MESENCHYMAL STEM-CELLS; MESOPOROUS SILICA NANOPARTICLES; NONVIRAL GENE DELIVERY; OSTEOGENIC DIFFERENTIATION; BONE REGENERATION; OSTEOBLAST DIFFERENTIATION; POSITIVE REGULATION; CALCIUM-CARBONATE; CALVARIAL DEFECT; SCAFFOLDS;
D O I
10.1042/BST20221448
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
microRNAs (miRs) have been reported over the decades as important regulators in bone development and bone regeneration. They play important roles in maintaining the stem cell signature as well as regulating stem cell fate decisions. Thus, delivering miRs and miR inhibitors to the defect site is a potential treatment towards craniofacial bone defects. However, there are challenges in translation of basic research to clinics, including the efficiency, specificity, and efficacy of miR manipulation methods and the safety of miR delivery systems. In this review, we will compare miR oligonucleotides, mimics and antagomirs as therapeutic reagents to treat disease and regenerate tissues. Newer technology will be discussed as well as the efficiency and efficacy of using these technologies to express or inhibit miRs in treating and repairing oral tissues. Delivery of these molecules using extracellular vesicles and nanoparticles can achieve different results and depending on their composition will elicit specific effects. We will highlight the specificity, toxicity, stability, and effectiveness of several miR systems in regenerative medicine.
引用
收藏
页码:841 / 854
页数:14
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