A Review of Recent Developments in the Molecular Mechanisms of Bone Healing

Int J Mol Sci. 2021 Jan 14;22(2):767. doi: 10.3390/ijms22020767.

Abstract

Between 5 and 10 percent of fractures do not heal, a condition known as nonunion. In clinical practice, stable fracture fixation associated with autologous iliac crest bone graft placement is the gold standard for treatment. However, some recalcitrant nonunions do not resolve satisfactorily with this technique. For these cases, biological alternatives are sought based on the molecular mechanisms of bone healing, whose most recent findings are reviewed in this article. The pro-osteogenic efficacy of morin (a pale yellow crystalline flavonoid pigment found in old fustic and osage orange trees) has recently been reported, and the combined use of bone morphogenetic protein-9 (BMP9) and leptin might improve fracture healing. Inhibition with methyl-piperidino-pyrazole of estrogen receptor alpha signaling delays bone regeneration. Smoking causes a chondrogenic disorder, aberrant activity of the skeleton's stem and progenitor cells, and an intense initial inflammatory response. Smoking cessation 4 weeks before surgery is therefore highly recommended. The delay in fracture consolidation in diabetic animals is related to BMP6 deficiency (35 kDa). The combination of bioceramics and expanded autologous human mesenchymal stem cells from bone marrow is a new and encouraging alternative for treating recalcitrant nonunions.

Keywords: angiogenesis; bone; bone tissue engineering; fracture; healing; osteoblasts; osteoclasts; osteogenesis; periosteum.

Publication types

  • Review

MeSH terms

  • Animals
  • Bone Substitutes / pharmacology
  • Bone Substitutes / therapeutic use
  • Flavonoids / pharmacology
  • Flavonoids / therapeutic use
  • Fracture Healing* / drug effects
  • Growth Differentiation Factor 2 / pharmacology
  • Growth Differentiation Factor 2 / therapeutic use
  • Humans
  • Leptin / pharmacology
  • Leptin / therapeutic use
  • Mesenchymal Stem Cell Transplantation
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism
  • Osteocytes / cytology
  • Osteocytes / drug effects
  • Osteocytes / metabolism
  • Osteogenesis* / drug effects

Substances

  • Bone Substitutes
  • Flavonoids
  • Growth Differentiation Factor 2
  • Leptin
  • morin