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.

Highlights

  • Transplantation of fetal and adult Mesenchymal stem/stromal cells (MSCs) in mouse models of osteogenesis imperfecta (OI) led to a decrease in long bone fracture rate, but failed to improve bone strength[23,24,25,26]

  • amniotic fluid mesenchymal stem cells (AFSCs) engrafted into bones and expressed osteoblast markers

  • AFSCs were thawed in expansion medium, plated at 104 cells/cm[2] and let to recover for 48 hours before being intraperitoneally infused (106 cells) into oim mouse neonates

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Summary

Introduction

Transplantation of fetal and adult MSCs in mouse models of osteogenesis imperfecta (OI) led to a decrease in long bone fracture rate, but failed to improve bone strength[23,24,25,26]. A number of observations support the hypothesis that donor cells mediated bone regeneration by direct cell replacement, we found that AFSCs transplantation promoted resident osteoblast maturation, stimulating endogenous osteogenesis and collagen production, thereby restoring the balance of bone remodelling. These results identify AFSCs as an ethical and available source of fetal stem cells that could be used as countermeasure to bone fragility

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