Literature DB >> 33309989

MicroRNA function in craniofacial bone formation, regeneration and repair.

Liu Hong1, Hongli Sun1, Brad A Amendt2.   

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.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

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

Mesh:

Substances:

Year:  2020        PMID: 33309989      PMCID: PMC7869528          DOI: 10.1016/j.bone.2020.115789

Source DB:  PubMed          Journal:  Bone        ISSN: 1873-2763            Impact factor:   4.398


  215 in total

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9.  A new plasmid-based microRNA inhibitor system that inhibits microRNA families in transgenic mice and cells: a potential new therapeutic reagent.

Authors:  H Cao; W Yu; X Li; J Wang; S Gao; N E Holton; S Eliason; T Sharp; B A Amendt
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  3 in total

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