Abstract

This study aimed to investigate if autologous bone marrow mesenchymal stem cells (MSCs) could treat osteonecrosis of the femoral head (ONFH) and what the fate and distribution of the cells are in dogs. Twelve Beagle dogs were randomly divided into two groups: MSCs group and SHAM operated group. After three weeks, dogs in MSCs group and SHAM operated group were intra-arterially injected with autologous MSCs and 0.9% normal saline, respectively. Eight weeks after treatment, the necrotic volume of the femoral heads was significantly reduced in MSCs group. Moreover, the trabecular bone volume was increased and the empty lacunae rate was decreased in MSCs group. In addition, the BrdU-positive MSCs were unevenly distributed in femoral heads and various vital organs. But no obvious abnormalities were observed. Furthermore, most of BrdU-positive MSCs in necrotic region expressed osteocalcin in MSCs group and a few expressed peroxisome proliferator-activated receptor-γ (PPAR-γ). Taken together, these data indicated that intra-arterially infused MSCs could migrate into the necrotic field of femoral heads and differentiate into osteoblasts, thus improving the necrosis of femoral heads. It suggests that intra-arterial infusion of autologous MSCs might be a feasible and relatively safe method for the treatment of femoral head necrosis.

Highlights

  • Osteonecrosis of the femoral head (ONFH) is a debilitating disease that frequently affects patients between 20 and 50 years old [1]

  • Recent studies showed that ONFH is highly related to the decrease or alterations of marrow mesenchymal stem cells (MSCs) or other progenitor cells in proximal femurs [9,10,11,12,13], and it is gradually accepted that ONFH originates from the cellular level [14,15,16]

  • We investigated if MSCs could treat ONFH and the fate and distribution of autologous MSCs with intra-arterial infusion in ONFH in dogs

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Summary

Introduction

Osteonecrosis of the femoral head (ONFH) is a debilitating disease that frequently affects patients between 20 and 50 years old [1]. The efficacy of these procedures remains either variable or controversial and palliative surgical interventions have disadvantages of difficult manipulation [2, 8]. It is badly in need of developing noninvasive or less-invasive and effective strategies to protect the femoral head from collapse. Recent studies showed that ONFH is highly related to the decrease or alterations of marrow mesenchymal stem cells (MSCs) or other progenitor cells in proximal femurs [9,10,11,12,13], and it is gradually accepted that ONFH originates from the cellular level [14,15,16]

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