Abstract

Mesenchymal stem/stromal cells (MSCs) are known to be useful for treating local bone diseases. However, it is not known if MSCs are effective for treating systemic bone diseases, as the risk for mortality following intravenous MSC administration has hindered research progress. In this study, we compared the safety and efficacy of intra-bone marrow and intravenous administration of MSCs for the treatment of ovariectomy- (OVX-) induced osteoporosis. Cells capable of forming bone were isolated from the murine compact bones and expanded in culture. Relatively pure MSCs possessing increased potential for cell proliferation, osteogenic differentiation, and inhibition of osteoclastogenesis were obtained by magnetic-activated cell sorting with the anti-Sca-1 antibody. Sca-1-sorted MSCs were administered to OVX mice, which were sacrificed 1 month later. We observed that 22% of the mice died after intravenous administration, whereas none of the mice died after intra-bone marrow administration. With respect to efficacy, intravenous administration improved bone mineral density (BMD) by increasing bone mineral content without affecting bone thickness, whereas intra-bone marrow administration improved BMD by increasing both bone mineral content and bone thickness. These results indicate that intra-bone marrow administration of pure MSCs is a safer and more effective approach for treating osteoporosis.

Highlights

  • Mesenchymal stem/stromal cells (MSCs) have attracted much interest as potent somatic stem cells for use in regenerative medicine in various tissues/organs because of their ability to differentiate into multiple lineages [1, 2]

  • Treating osteoporosis with bone marrow transplantation is unrealistic, this study showed that MSCs, as well as hematolymphoid cells, could be efficiently transplanted by intra-bone marrow injection

  • MSCs are comprised of a heterogeneous mixture of various cell populations including stem cells [11, 13], multipotent MSCs in mice express CD29 and Sca-1 but not CD11b or CD45 [11, 13, 14]

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Summary

Introduction

Mesenchymal stem/stromal cells (MSCs) have attracted much interest as potent somatic stem cells for use in regenerative medicine in various tissues/organs because of their ability to differentiate into multiple lineages (osteogenic, chondrogenic, adipogenic, myogenic, and neurogenic) [1, 2]. MSCs have recently gained attention as immunosuppressive cells that may be effective for treating immunological disorders such as graft-versus-host disease [3]. MSCs are considered therapeutically useful cells, and their clinical use is expected to increase in the future. Because MSCs were originally identified as osteogenic stem/progenitor cells [4], potential therapeutic applications for bone tissue treatment have been extensively studied [5, 6]. Stem Cells International even autologous bone grafting [5]. MSCs may be applicable for treating systemic bone diseases such as osteoporosis

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