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      Engineered scaffolds based on mesenchymal stem cells/preosteoclasts extracellular matrix promote bone regeneration

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          Abstract

          Recently, extracellular matrix-based tissue-engineered bone is a promising approach to repairing bone defects, and the seed cells are mostly mesenchymal stem cells. However, bone remodelling is a complex biological process, in which osteoclasts perform bone resorption and osteoblasts dominate bone formation. The interaction and coupling of these two kinds of cells is the key to bone repair. Therefore, the extracellular matrix secreted by the mesenchymal stem cells alone cannot mimic a complex bone regeneration microenvironment, and the addition of extracellular matrix by preosteoclasts may contribute as an effective strategy for bone regeneration. Here, we established the mesenchymal stem cell/preosteoclast extracellular matrix -based tissue-engineered bones and demonstrated that engineered-scaffolds based on mesenchymal stem cell/ preosteoclast extracellular matrix significantly enhanced osteogenesis in a 3 mm rat femur defect model compared with mesenchymal stem cell alone. The bioactive proteins released from the mesenchymal stem cell/ preosteoclast extracellular matrix based tissue-engineered bones also promoted the migration, adhesion, and osteogenic differentiation of mesenchymal stem cells in vitro. As for the mechanisms, the iTRAQ-labeled mass spectrometry was performed, and 608 differentially expressed proteins were found, including the IGFBP5 and CXCL12. Through in vitro studies, we proved that CXCL12 and IGFBP5 proteins, mainly released from the preosteoclasts, contributed to mesenchymal stem cells migration and osteogenic differentiation, respectively. Overall, our research, for the first time, introduce pre-osteoclast into the tissue engineering of bone and optimize the strategy of constructing extracellular matrix–based tissue-engineered bone using different cells to simulate the natural bone regeneration environment, which provides new sight for bone tissue engineering.

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          Most cited references38

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          Current State of Fabrication Technologies and Materials for Bone Tissue Engineering

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            Osteoclasts Provide Coupling Signals to Osteoblast Lineage Cells Through Multiple Mechanisms

            Bone remodeling is essential for the repair and replacement of damaged and old bone. The major principle underlying this process is that osteoclast-mediated resorption of a quantum of bone is followed by osteoblast precursor recruitment; these cells differentiate to matrix-producing osteoblasts, which form new bone to replace what was resorbed. Evidence from osteopetrotic syndromes indicate that osteoclasts not only resorb bone, but also provide signals to promote bone formation. Osteoclasts act upon osteoblast lineage cells throughout their differentiation by facilitating growth factor release from resorbed matrix, producing secreted proteins and microvesicles, and expressing membrane-bound factors. These multiple mechanisms mediate the coupling of bone formation to resorption in remodeling. Additional interactions of osteoclasts with osteoblast lineage cells, including interactions with canopy and reversal cells, are required to achieve coordination between bone formation and resorption during bone remodeling.
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              Immunological aspects of allogeneic mesenchymal stem cell therapies.

              Allogeneic mesenchymal stem or stromal cells (MSCs) are proposed as cell therapies for degenerative, inflammatory, and autoimmune diseases. The feasibility of allogeneic MSC therapies rests heavily on the concept that these cells avoid or actively suppress the immunological responses that cause rejection of most allogeneic cells and tissues. In this article the validity of the immune privileged status of allogeneic MSCs is explored in the context of recent literature. Current data that provide the mechanistic basis for immune modulation by MSCs are reviewed with particular attention to how MSCs modify the triggering and effector functions of innate and adaptive immunity. The ability of MSCs to induce regulatory dendritic and T-cell populations is discussed with regard to cell therapy for autoimmune disease. Finally, we examine the evidence for and against the immune privileged status of allogeneic MSCs in vivo. Allogeneic MSCs emerge as cells that are responsive to local signals and exert wide-ranging, predominantly suppressive, effects on innate and adaptive immunity. Nonetheless, these cells also retain a degree of immunogenicity in some circumstances that may limit MSC longevity and attenuate their beneficial effects. Ultimately successful allogeneic cell therapies will rely on an improved understanding of the parameters of MSC-immune system interactions in vivo.
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                Author and article information

                Journal
                J Tissue Eng
                J Tissue Eng
                TEJ
                sptej
                Journal of Tissue Engineering
                SAGE Publications (Sage UK: London, England )
                2041-7314
                7 June 2020
                Jan-Dec 2020
                : 11
                : 2041731420926918
                Affiliations
                [1 ]Department of Biomedical Materials Science, School of Biomedical Engineering, Third Military Medical University, Chongqing, China
                [2 ]Department of Orthopedics, Southwest Hospital, Third Military Medical University, Chongqing, China
                [3 ]State Key Laboratory of Trauma, Burns and Combined Injury, Third Military Medical University, Chongqing, China
                Author notes
                [*]Shiwu Dong, Department of Biomedical Materials Science, School of Biomedical Engineering, Third Military Medical University, Gaotanyan Street No. 30, Chongqing 400038, China. Email: dongshiwu@ 123456tmmu.edu.cn
                [*]

                These authors contributed equally to this work

                Author information
                https://orcid.org/0000-0002-5032-4893
                Article
                10.1177_2041731420926918
                10.1177/2041731420926918
                7278336
                32551034
                818cd897-336a-4db2-ad01-12e3bc958a2d
                © The Author(s) 2020

                This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License ( https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page ( https://us.sagepub.com/en-us/nam/open-access-at-sage).

                History
                : 2 January 2020
                : 26 April 2020
                Funding
                Funded by: national natural science foundation of china, FundRef https://doi.org/10.13039/501100001809;
                Award ID: 31870962
                Funded by: national natural science foundation of china, FundRef https://doi.org/10.13039/501100001809;
                Award ID: 81930067
                Funded by: southwest hospital, FundRef https://doi.org/10.13039/501100011476;
                Award ID: SWH2018LJ-03
                Funded by: the Medical Science and Technology Youth Cultivation Project of PLA, ;
                Award ID: 20QNPY022
                Funded by: third military medical university, FundRef https://doi.org/10.13039/501100007055;
                Award ID: 2018XYY05
                Funded by: the Key Project of Logistics Research Plan of the PLA, ;
                Award ID: AWS17J004
                Categories
                Original Article
                Custom metadata
                January-December 2020
                ts1

                Biomedical engineering
                msc/poc ecm-based teb,bone regeneration,extracellular matrix proteins,igfbp5,cxcl12

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