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      iPSCs: A powerful tool for skeletal muscle tissue engineering

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          Abstract

          Both volumetric muscle loss ( VML) and muscle degenerative diseases lead to an important decrease in skeletal muscle mass, condition that nowadays lacks an optimal treatment. This issue has driven towards an increasing interest in new strategies in tissue engineering, an emerging field that can offer very promising approaches. In addition, the discovery of induced pluripotent stem cells ( iPSCs) has completely revolutionized the actual view of personalized medicine, and their utilization in skeletal muscle tissue engineering could, undoubtedly, add myriad benefits. In this review, we want to provide a general vision of the basic aspects to consider when engineering skeletal muscle tissue using iPSCs. Specifically, we will focus on the three main pillars of tissue engineering: the scaffold designing, the selection of the ideal cell source and the addition of factors that can enhance the resemblance with the native tissue.

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          Most cited references59

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          3D bioprinting for engineering complex tissues.

          Bioprinting is a 3D fabrication technology used to precisely dispense cell-laden biomaterials for the construction of complex 3D functional living tissues or artificial organs. While still in its early stages, bioprinting strategies have demonstrated their potential use in regenerative medicine to generate a variety of transplantable tissues, including skin, cartilage, and bone. However, current bioprinting approaches still have technical challenges in terms of high-resolution cell deposition, controlled cell distributions, vascularization, and innervation within complex 3D tissues. While no one-size-fits-all approach to bioprinting has emerged, it remains an on-demand, versatile fabrication technique that may address the growing organ shortage as well as provide a high-throughput method for cell patterning at the micrometer scale for broad biomedical engineering applications. In this review, we introduce the basic principles, materials, integration strategies and applications of bioprinting. We also discuss the recent developments, current challenges and future prospects of 3D bioprinting for engineering complex tissues. Combined with recent advances in human pluripotent stem cell technologies, 3D-bioprinted tissue models could serve as an enabling platform for high-throughput predictive drug screening and more effective regenerative therapies.
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            Scaffolding in tissue engineering: general approaches and tissue-specific considerations.

            B Chan, K Leong (2008)
            Scaffolds represent important components for tissue engineering. However, researchers often encounter an enormous variety of choices when selecting scaffolds for tissue engineering. This paper aims to review the functions of scaffolds and the major scaffolding approaches as important guidelines for selecting scaffolds and discuss the tissue-specific considerations for scaffolding, using intervertebral disc as an example.
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              Pluripotent stem cells in disease modelling and drug discovery.

              Experimental modelling of human disorders enables the definition of the cellular and molecular mechanisms underlying diseases and the development of therapies for treating them. The availability of human pluripotent stem cells (PSCs), which are capable of self-renewal and have the potential to differentiate into virtually any cell type, can now help to overcome the limitations of animal models for certain disorders. The ability to model human diseases using cultured PSCs has revolutionized the ways in which we study monogenic, complex and epigenetic disorders, as well as early- and late-onset diseases. Several strategies are used to generate such disease models using either embryonic stem cells (ES cells) or patient-specific induced PSCs (iPSCs), creating new possibilities for the establishment of models and their use in drug screening.
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                Author and article information

                Contributors
                egallardo.imas12@h12o.es
                Journal
                J Cell Mol Med
                J. Cell. Mol. Med
                10.1111/(ISSN)1582-4934
                JCMM
                Journal of Cellular and Molecular Medicine
                John Wiley and Sons Inc. (Hoboken )
                1582-1838
                1582-4934
                01 April 2019
                June 2019
                : 23
                : 6 ( doiID: 10.1111/jcmm.2019.23.issue-6 )
                : 3784-3794
                Affiliations
                [ 1 ] Departamento de Bioquímica Facultad de Medicina Instituto de Investigaciones Biomédicas “Alberto Sols”, Universidad Autónoma de Madrid, Spain, (UAM‐CSIC) Madrid Spain
                [ 2 ] Instituto de Investigación Sanitaria Hospital 12 de Octubre (i+12) Madrid Spain
                [ 3 ] Grupo de Investigación Traslacional con células iPS Instituto de Investigación Sanitaria Hospital 12 de Octubre (i+12) Madrid Spain
                [ 4 ] Centro de Investigación Biomédica en Red (CIBERER) Madrid Spain
                Author notes
                [*] [* ] Correspondence

                María Esther Gallardo, Grupo de Investigación Traslacional con Células iPS, Instituto de Investigación Sanitaria Hospital 12 de Octubre (i+12), Madrid, Spain.

                Email: egallardo.imas12@ 123456h12o.es

                [†]

                These authors contributed equally.

                Author information
                https://orcid.org/0000-0002-8699-8734
                Article
                JCMM14292
                10.1111/jcmm.14292
                6533516
                30933431
                66481ee3-2d84-486b-a85e-2b457abbc301
                © 2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 18 January 2019
                : 05 March 2019
                : 08 March 2019
                Page count
                Figures: 3, Tables: 1, Pages: 11, Words: 8467
                Funding
                Funded by: Fondo de Investigación Sanitaria
                Funded by: FEDER Funds
                Funded by: Ministerio de Educación, Cultura y Deporte
                Funded by: Instituto de Investigación Sanitaria Hospital 12 de Octubre, i+12
                Categories
                Review
                Reviews
                Custom metadata
                2.0
                jcmm14292
                June 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.6.3 mode:remove_FC converted:24.05.2019

                Molecular medicine
                biomaterials,induced pluripotent stem cells,ipscs,ips‐skeletal muscle,personalized medicine,regenerative medicine,scaffold,tissue engineering,volumetric muscle loss

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