The role of microRNAs in the osteogenic and chondrogenic differentiation of mesenchymal stem cells and bone pathologies

Theranostics. 2021 Apr 30;11(13):6573-6591. doi: 10.7150/thno.55664. eCollection 2021.

Abstract

Mesenchymal stem cells (MSCs) have been identified in many adult tissues. MSCs can regenerate through cell division or differentiate into adipocytes, osteoblasts and chondrocytes. As a result, MSCs have become an important source of cells in tissue engineering and regenerative medicine for bone tissue and cartilage. Several epigenetic factors are believed to play a role in MSCs differentiation. Among these, microRNA (miRNA) regulation is involved in the fine modulation of gene expression during osteogenic/chondrogenic differentiation. It has been reported that miRNAs are involved in bone homeostasis by modulating osteoblast gene expression. In addition, countless evidence has demonstrated that miRNAs dysregulation is involved in the development of osteoporosis and bone fractures. The deregulation of miRNAs expression has also been associated with several malignancies including bone cancer. In this context, bone-associated circulating miRNAs may be useful biomarkers for determining the predisposition, onset and development of osteoporosis, as well as in clinical applications to improve the diagnosis, follow-up and treatment of cancer and metastases. Overall, this review will provide an overview of how miRNAs activities participate in osteogenic/chondrogenic differentiation, while addressing the role of miRNA regulatory effects on target genes. Finally, the role of miRNAs in pathologies and therapies will be presented.

Keywords: MSC differentiation; disease; epigenetics; microRNAs; tumour.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Bone Diseases / genetics*
  • Bone Morphogenetic Proteins / physiology
  • Chondrogenesis / genetics*
  • Core Binding Factor Alpha 1 Subunit / physiology
  • Drug Delivery Systems
  • Fractures, Bone / metabolism
  • Histone Deacetylases / physiology
  • Humans
  • Matrix Metalloproteinase 13 / physiology
  • Mesenchymal Stem Cells / cytology*
  • MicroRNAs / genetics*
  • Osteogenesis / genetics*
  • Repressor Proteins / physiology
  • Signal Transduction
  • Smad Proteins / physiology
  • Sp7 Transcription Factor / physiology
  • Transforming Growth Factor beta / physiology
  • Vascular Endothelial Growth Factor A / physiology

Substances

  • Bone Morphogenetic Proteins
  • Core Binding Factor Alpha 1 Subunit
  • MicroRNAs
  • Repressor Proteins
  • Smad Proteins
  • Sp7 Transcription Factor
  • Sp7 protein, mouse
  • Transforming Growth Factor beta
  • Vascular Endothelial Growth Factor A
  • Matrix Metalloproteinase 13
  • HDAC4 protein, human
  • Histone Deacetylases