Counteracting bone fragility with human amniotic mesenchymal stem cells

Sci Rep. 2016 Dec 20:6:39656. doi: 10.1038/srep39656.

Abstract

The impaired maturation of bone-forming osteoblasts results in reduced bone formation and subsequent bone weakening, which leads to a number of conditions such as osteogenesis imperfecta (OI). Transplantation of human fetal mesenchymal stem cells has been proposed as skeletal anabolic therapy to enhance bone formation, but the mechanisms underlying the contribution of the donor cells to bone health are poorly understood and require further elucidation. Here, we show that intraperitoneal injection of human amniotic mesenchymal stem cells (AFSCs) into a mouse model of OI (oim mice) reduced fracture susceptibility, increased bone strength, improved bone quality and micro-architecture, normalised bone remodelling and reduced TNFα and TGFβ sigalling. Donor cells engrafted into bones and differentiated into osteoblasts but importantly, also promoted endogenous osteogenesis and the maturation of resident osteoblasts. Together, these findings identify AFSC transplantation as a countermeasure to bone fragility. These data have wider implications for bone health and fracture reduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amnion / cytology*
  • Animals
  • Bone Remodeling
  • Bone and Bones / metabolism
  • Cell Differentiation
  • Disease Models, Animal
  • Female
  • Flow Cytometry
  • Fractures, Bone / prevention & control*
  • Gene Expression Profiling
  • Genetic Markers
  • Humans
  • Male
  • Mesenchymal Stem Cell Transplantation*
  • Mesenchymal Stem Cells / cytology*
  • Mice
  • Osteoblasts / metabolism
  • Osteogenesis
  • Osteogenesis Imperfecta / prevention & control*
  • Stress, Mechanical
  • Transforming Growth Factor beta / metabolism
  • Tumor Necrosis Factor-alpha / metabolism
  • X-Ray Microtomography

Substances

  • Genetic Markers
  • Transforming Growth Factor beta
  • Tumor Necrosis Factor-alpha