MicroRNA function in craniofacial bone formation, regeneration and repair

Bone. 2021 Mar:144:115789. doi: 10.1016/j.bone.2020.115789. Epub 2020 Dec 9.

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.

Keywords: Bone development; Bone regeneration; Bone repair; microRNA inhibitor system (PMIS); microRNA mouse models; microRNA therapeutic.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Animals
  • Bone Regeneration* / genetics
  • Humans
  • Maxilla
  • MicroRNAs* / genetics
  • Neural Crest
  • Osteogenesis* / genetics
  • Skull

Substances

  • MicroRNAs