The Application of microRNAs in Biomaterial Scaffold-Based Therapies for Bone Tissue Engineering

Biotechnol J. 2019 Oct;14(10):e1900084. doi: 10.1002/biot.201900084. Epub 2019 Jul 9.

Abstract

In recent years, the application of microRNAs (miRNAs) or anti-microRNAs (anti-miRNAs) that can induce expression of the runt-related transcription factor 2 (RUNX2), a master regulator of osteogenesis, has been investigated as a promising alternative bone tissue engineering strategy. In this review, biomaterial scaffold-based applications that have been used to deliver cells expressing miRNAs or anti-miRNAs that induce expression of RUNX2 for bone tissue engineering are discussed. An overview of the components of the scaffold-based therapies including the miRNAs/anti-miRNAs, cell types, gene delivery vectors, and scaffolds that have been applied are provided. To date, there have been nine miRNAs/anti-miRNAs (i.e., miRNA-26a, anti-miRNA-31, anti-miRNA-34a, miRNA-135, anti-miRNA-138, anti-miRNA-146a, miRNA-148b, anti-miRNA-221, and anti-miRNA-335) that have been incorporated into scaffold-based bone tissue engineering applications and investigated in an in vivo bone critical-sized defect model. For all of the biomaterial scaffold-based miRNA therapies that have been developed thus far, cells that are transfected or transduced with the miRNA/anti-miRNA are loaded into the scaffolds and implanted at the site of interest instead of locally delivering the miRNA/anti-miRNAs directly from the scaffolds. Thus, future work may focus on developing biomaterial scaffolds to deliver miRNAs or anti-miRNAs into cells in vivo.

Keywords: biomaterials; bone tissue engineering; gene therapy; microRNAs; scaffolds.

Publication types

  • Review

MeSH terms

  • Animals
  • Bone Transplantation
  • Bone and Bones / metabolism*
  • Core Binding Factor Alpha 1 Subunit / metabolism*
  • Humans
  • MicroRNAs / genetics*
  • Tissue Engineering
  • Tissue Scaffolds
  • Wnt Signaling Pathway

Substances

  • Core Binding Factor Alpha 1 Subunit
  • MicroRNAs
  • RUNX2 protein, human