Abstract

Bone marrow-derived mesenchymal stem cells (BM-MSCs) are the most valuable source of autologous cells for transplantation and tissue regeneration to treat osteoporosis. Although BM-MSCs are the primary cells responsible for maintaining bone metabolism and homeostasis, their regenerative ability may be attenuated in postmenopausal osteoporosis patients. Therefore, we first examined potential abnormalities of BM-MSCs in an oestrogen-deficient rat model constructed by ovariectomy (OVX-MSCs). Cell proliferation, mobilisation, and regulation of osteoclasts were downregulated in OVX-MSCs. Moreover, therapeutic effects of OVX-MSCs were decreased in OVX rats. Accordingly, we developed a new activator for BM-MSCs using human umbilical cord extracts, Wharton’s jelly extract supernatant (WJS), which improved cell proliferation, mobilisation and suppressive effects on activated osteoclasts in OVX-MSCs. Bone volume, RANK and TRACP expression of osteoclasts, as well as proinflammatory cytokine expression in bone tissues, were ameliorated by OVX-MSCs activated with WJS (OVX-MSCs-WJ) in OVX rats. Fusion and bone resorption activity of osteoclasts were suppressed in macrophage-induced and primary mouse bone marrow cell-induced osteoclasts via suppression of osteoclast-specific genes, such as Nfatc1, Clcn7, Atp6i and Dc-stamp, by co-culture with OVX-MSCs-WJ in vitro. In this study, we developed a new activator, WJS, which improved the functional abnormalities and therapeutic effects of BM-MSCs on postmenopausal osteoporosis.

Highlights

  • Bone marrow-derived mesenchymal stem cells (BM-MSCs) are the most valuable source of autologous cells for transplantation and tissue regeneration to treat osteoporosis

  • BM-MSCs derived from sham-operated rats (Sham-MSCs) but not OVX rats (OVX-MSCs) ameliorated osteoporosis in OVX rats

  • Serum tartrate-resistant acid phosphatase (TRACP) levels were significantly higher in OVX-Vehicle rats and OVX-OVX-MSCs rats compared with sham operation (Sham) rats (P = 0.011, OVX-Vehicle vs. Sham; P = 0.047, OVX-OVX-MSCs vs. Sham; Fig. 1j), while they were significantly lower in OVX-Sham-MSCs rats compared with OVX-Vehicle and OVX-OVX-MSC rats 8 weeks after the administration of each type of BM-MSC (P = 0.004, OVX-Sham-MSC vs. OVX-Vehicle; P = 0.022, OVX-Sham-MSCs vs. OVX-OVX-MSCs; Fig. 1j)

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Summary

Introduction

Bone marrow-derived mesenchymal stem cells (BM-MSCs) are the most valuable source of autologous cells for transplantation and tissue regeneration to treat osteoporosis. We developed a new activator, WJS, which improved the functional abnormalities and therapeutic effects of BM-MSCs on postmenopausal osteoporosis. Autologous transplantation of BM-MSCs has great benefits because of a low risk of rejection and exogenous infection, as well as the availability of a stable source of MSCs. several functional abnormalities of BM-MSCs have been reported in osteoporosis patients[13,14,15], which suggested that BM-MSCs derived from patients are unsuitable for cell therapy. We first aimed to investigate whether abnormal BM-MSCs derived from an oestrogen-deficient osteoporosis model exhibit sufficient therapeutic effects on osteoporosis in vivo, and clarified the abnormalities of BM-MSCs by focusing on the regulation of osteoclast activity in vitro. We investigated the therapeutic effects of activated BM-MSCs on the OVX model in vivo

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