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MicroRNA function in craniofacial bone formation, regeneration and repair
Journal article   Peer reviewed

MicroRNA function in craniofacial bone formation, regeneration and repair

Liu Hong, Hongli Sun and Brad A. Amendt
Bone (New York, N.Y.), Vol.144, pp.115789-115789
03/2021
DOI: 10.1016/j.bone.2020.115789
PMCID: PMC7869528
PMID: 33309989
url
https://www.ncbi.nlm.nih.gov/pmc/articles/7869528View
Open Access

Abstract

Bone formation in the craniofacial complex is regulated by cranial neural crest (CNC) and mesoderm-derived cells. Different elements of the developing skull, face, mandible, maxilla (jaws) and nasal bones are regulated by an array of transcription factors, signaling molecules and microRNAs (miRs). miRs are molecular modulators of these factors and act to restrict their expression in a temporal-spatial mechanism. miRs control the different genetic pathways that form the craniofacial complex. By understanding how miRs function in vivo during development they can be adapted to regenerate and repair craniofacial genetic anomalies as well as bone diseases and defects due to traumatic injuries. This review will highlight some of the new miR technologies and functions that form new bone or inhibit bone regeneration. [Display omitted] •MicroRNAs regulate genetic pathways that form bone and inhibit bone regeneration.•New microRNA inhibition technology (PMIS) proven in transgenic mice models•MicroRNAs regulate bone formation, inflammation, osteoporosis and periodontitis.•New microRNA inhibition technology (PMIS) more efficacious than oligonucleotides•MicroRNA gene therapy approaches are compared to stem cell-based scaffolds.
Bone development Bone regeneration Bone repair microRNA inhibitor system (PMIS) microRNA mouse models microRNA therapeutic

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