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      In vivo engineered extracellular matrix scaffolds with instructive niches for oriented tissue regeneration

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          Abstract

          Implanted scaffolds with inductive niches can facilitate the recruitment and differentiation of host cells, thereby enhancing endogenous tissue regeneration. Extracellular matrix (ECM) scaffolds derived from cultured cells or natural tissues exhibit superior biocompatibility and trigger favourable immune responses. However, the lack of hierarchical porous structure fails to provide cells with guidance cues for directional migration and spatial organization, and consequently limit the morpho-functional integration for oriented tissues. Here, we engineer ECM scaffolds with parallel microchannels (ECM-C) by subcutaneous implantation of sacrificial templates, followed by template removal and decellularization. The advantages of such ECM-C scaffolds are evidenced by close regulation of in vitro cell activities, and enhanced cell infiltration and vascularization upon in vivo implantation. We demonstrate the versatility and flexibility of these scaffolds by regenerating vascularized and innervated neo-muscle, vascularized neo-nerve and pulsatile neo-artery with functional integration. This strategy has potential to yield inducible biomaterials with applications across tissue engineering and regenerative medicine.

          Abstract

          Extracellular matrix (ECM) is an ideal scaffold for tissue engineering but tends to lack hierarchical structure. Here the authors implant sacrificial templates subcutaneously to build an organised ECM scaffold, and following template removal and decellularisation use these scaffolds to create functionally integrated muscle, nerve and artery in vivo.

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          An overview of tissue and whole organ decellularization processes.

          Biologic scaffold materials composed of extracellular matrix (ECM) are typically derived by processes that involve decellularization of tissues or organs. Preservation of the complex composition and three-dimensional ultrastructure of the ECM is highly desirable but it is recognized that all methods of decellularization result in disruption of the architecture and potential loss of surface structure and composition. Physical methods and chemical and biologic agents are used in combination to lyse cells, followed by rinsing to remove cell remnants. Effective decellularization methodology is dictated by factors such as tissue density and organization, geometric and biologic properties desired for the end product, and the targeted clinical application. Tissue decellularization with preservation of ECM integrity and bioactivity can be optimized by making educated decisions regarding the agents and techniques utilized during processing. An overview of decellularization methods, their effect upon resulting ECM structure and composition, and recently described perfusion techniques for whole organ decellularization techniques are presented herein. Copyright © 2011 Elsevier Ltd. All rights reserved.
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            Inactivation of porcine endogenous retrovirus in pigs using CRISPR-Cas9

            Xenotransplantation is a promising strategy to alleviate the shortage of organs for human transplantation. In addition to the concern on pig-to-human immunological compatibility, the risk of cross-species transmission of porcine endogenous retroviruses (PERVs) has impeded the clinical application of this approach. Earlier, we demonstrated the feasibility of inactivating PERV activity in an immortalized pig cell line. Here, we confirmed that PERVs infect human cells, and observed the horizontal transfer of PERVs among human cells. Using CRISPR-Cas9, we inactivated all the PERVs in a porcine primary cell line and generated PERV-inactivated pigs via somatic cell nuclear transfer. Our study highlighted the value of PERV inactivation to prevent cross-species viral transmission and demonstrated the successful production of PERV-inactivated animals to address the safety concern in clinical xenotransplantation.
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              Extracellular matrix-based materials for regenerative medicine

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                Author and article information

                Contributors
                wkcs424@163.com
                hongjun.wang@stevens.edu
                kongdeling@nankai.edu.cn
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                11 October 2019
                11 October 2019
                2019
                : 10
                : 4620
                Affiliations
                [1 ]ISNI 0000 0000 9878 7032, GRID grid.216938.7, College of Life Science, Key Laboratory of Bioactive Materials (Ministry of Education), State Key Laboratory of Medicinal Chemical Biology, Xu Rongxiang Regeneration Life Science Center, , Nankai University, ; 300071 Tianjin, China
                [2 ]ISNI 0000 0001 2180 0654, GRID grid.217309.e, Department of Biomedical Engineering, , Stevens Institute of Technology, ; Hoboken, NJ 07030 USA
                [3 ]ISNI 0000 0000 9792 1228, GRID grid.265021.2, Tianjin Key Laboratory of Medical Epigenetics, , Tianjin Medical University, ; Tianjin, China
                [4 ]ISNI 0000000086837370, GRID grid.214458.e, Department of Biologic and Materials Sciences, Department of Biomedical Engineering, Macromolecular Science and Engineering Centre, Department of Materials Science and Engineering, , University of Michigan, ; Ann Arbor, MI 48109 USA
                Author information
                http://orcid.org/0000-0002-7622-0275
                http://orcid.org/0000-0002-0191-9487
                Article
                12545
                10.1038/s41467-019-12545-3
                6789018
                31604958
                12b91ee4-9ca6-45a1-b4ea-42a3fed2e876
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 6 September 2018
                : 12 September 2019
                Funding
                Funded by: National Natural Science Foundation of China (NSFC) projects (81772000)
                Funded by: National Science Foundation (NSF-DMR award number 1508511) and NIAMS award number 1R01AR067859
                Funded by: National Key Research and Development Program of China (2017YFC1103500), Innovative Research Group Project (81921004), National Natural Science Foundation of China (NSFC) projects (81972063), Science and Technology Support Program of Tianjin (16YFZCSY01020)
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                regenerative medicine,tissue engineering,translational research,biomedical engineering

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