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      Asperosaponin VI stimulates osteogenic differentiation of rat adipose-derived stem cells

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          Abstract

          In the aging population, the decrease on osteogenic differentiation resulted into a significant reduction in bone formation. Bone tissue engineering has been a successful technique for treatment of bone defects. It is reported that adipose-derived stem cells (ADSCs) have pluripotency to differentiate into adipocytes and osteoblasts. However little is revealed about the effect of the herbal medicine Asperosaponin VI (ASA VI) on ADSCs differentiation. In our study, we isolated and identified ADSCs from rats. We examined the effect of different concentrations of ASA VI in ADSCs on alkaline phosphatase (ALP) activity, calcium deposition, the expression of bone-related proteins and the release of inflammatory cytokines. Flowcytometry assay showed ADSCs were highly expressed CD44 and CD105, but hardly expressed CD34 and CD45, suggesting ADSCs were successfully isolated for follow-up experiments. ALP activity examination and Alizarin red (AR) stain showed that ASA VI enhanced the ALP activity and promoted matrix mineralization in ADSCs. In addition, bone-related protein OCN and RUNX2, and Smad2/3 phosphorylation was upregulated after ASA VI treatment in ADSCs. ELISA results showed that ASA VI blocked the release of TNF-α, IL-6 and IL-1β in ADSCs. Considering this results, we concluded that ASA VI promotes osteogenic differentiation of ADSCs through inducing the expression of bone-related proteins. These findings enriched the function of ASA VI as a regenerative medicine and shed new light for the treatment of bone defects in clinical research.

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          Most cited references28

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          Bone remodelling at a glance.

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            Flavonoids of Herba Epimedii regulate osteogenesis of human mesenchymal stem cells through BMP and Wnt/beta-catenin signaling pathway.

            Herba Epimedii is one of the most commonly used Chinese herbs for treating osteoporosis. In the present study, the flavonoids of Herba Epimedii (HEF) have shown to promote the osteogenic differentiation of human bone marrow-derived mesenchymal stem cells. They were noted to enhance the mRNA expression of BMP-2, BMP-4, Runx2, beta-catenin and cyclinD1, all of which are BMP or Wnt-signaling pathway related regulators. The osteogenic effect was inhibited by the introduction of noggin and DKK-1, which is classical inhibitor of BMP and Wnt/beta-catenin signaling, respectively. These results suggest that HEF exerts promoting effect on osteogenic differentiation, which plausibly functions via the BMP and Wnt/beta-catenin signaling pathways. Considering the therapeutic efficiency and economical issues, HEF may be a potential candidate for promoting bone regeneration. On the other hand, osteogenic differentiation of MSCs may also be a promising and attractive tool to apply in bone repair.
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              Role of mesenchymal stem cells in regenerative medicine: application to bone and cartilage repair.

              Mesenchymal stem cells (MSC) are multipotent cells with the ability to differentiate into mesenchyme-derived cells including osteoblasts and chondrocytes. To provide an overview and expert opinion on the in vivo ability of MSC to home into tissues, their regenerative properties and potential applications for cell-based therapies to treat bone and cartilage disorders. Data sources including the PubMed database, abstract booklets and conference proceedings were searched for publications pertinent to MSC and their properties with emphasis on the in vivo studies and clinical use in cartilage and bone regeneration and repair. The search included the most current information possible. MSC can migrate to injured tissues and some of their reparative properties are mediated by paracrine mechanisms including their immunomodulatory actions. MSC possess a critical potential in regenerative medicine for the treatment of skeletal diseases, such as osteoarthritis or fracture healing failure, where treatments are partially effective or palliative.
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                Author and article information

                Contributors
                Journal
                Regen Ther
                Regen Ther
                Regenerative Therapy
                Japanese Society for Regenerative Medicine
                2352-3204
                10 May 2019
                December 2019
                10 May 2019
                : 11
                : 17-24
                Affiliations
                [a ]Department of Pediatric Orthopaedics, Henan Luoyang Orthopedic Hospital (Henan Provincial Orthopedic Hospital), China
                [b ]Joint Department, Henan Luoyang Orthopedic Hospital (Henan Provincial Orthopedic Hospital), China
                [c ]Pharmacy Department, Henan Luoyang Orthopedic Hospital (Henan Provincial Orthopedic Hospital), China
                Author notes
                []Corresponding author. Joint Department, Henan Luoyang Orthopedic Hospital (Henan Provincial Orthopedic Hospital), No. 100 yongping Road, zhengdong new district, zhengzhou, Henan, 471002, China. sunyongqiangsyq@ 123456163.com
                Article
                S2352-3204(18)30087-7
                10.1016/j.reth.2019.03.007
                6518317
                5fc81d08-3d6c-413d-812f-da02444fdd34
                ©?2019 The Japanese Society for Regenerative Medicine. Production and hosting by Elsevier B.V.

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 11 November 2018
                : 14 February 2019
                : 20 March 2019
                Categories
                Original Article

                asperosaponin vi,adipose-derived stem cells,osteogenic differentiation,bone defects,asa vi, asperosaponin vi,mscs, mesenchymal stem cells,adscs, adipose-derived stem cells,runx2, runt-related transcription factor 2,ocn, osteocalcin,alp, alkaline phosphatase,ar, alizarin red,pe, phycoerythrin

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