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      Design of biomimetic cellular scaffolds for co-culture system and their application

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          Abstract

          The extracellular matrix of most natural tissues comprises various types of cells, including fibroblasts, stem cells, and endothelial cells, which communicate with each other directly or indirectly to regulate matrix production and cell functionality. To engineer multicellular interactions in vitro, co-culture systems have achieved tremendous success achieving a more realistic microenvironment of in vivo metabolism than monoculture system in the past several decades. Recently, the fields of tissue engineering and regenerative medicine have primarily focused on three-dimensional co-culture systems using cellular scaffolds, because of their physical and biological relevance to the extracellular matrix of actual tissues. This review discusses several materials and methods to create co-culture systems, including hydrogels, electrospun fibers, microfluidic devices, and patterning for biomimetic co-culture system and their applications for specific tissue regeneration. Consequently, we believe that culture systems with appropriate physical and biochemical properties should be developed, and direct or indirect cell–cell interactions in the remodeled tissue must be considered to obtain an optimal tissue-specific microenvironment.

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          Most cited references103

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          Capturing complex 3D tissue physiology in vitro.

          The emergence of tissue engineering raises new possibilities for the study of complex physiological and pathophysiological processes in vitro. Many tools are now available to create 3D tissue models in vitro, but the blueprints for what to make have been slower to arrive. We discuss here some of the 'design principles' for recreating the interwoven set of biochemical and mechanical cues in the cellular microenvironment, and the methods for implementing them. We emphasize applications that involve epithelial tissues for which 3D models could explain mechanisms of disease or aid in drug development.
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            Tight junctions: from simple barriers to multifunctional molecular gates.

            Epithelia and endothelia separate different tissue compartments and protect multicellular organisms from the outside world. This requires the formation of tight junctions, selective gates that control paracellular diffusion of ions and solutes. Tight junctions also form the border between the apical and basolateral plasma-membrane domains and are linked to the machinery that controls apicobasal polarization. Additionally, signalling networks that guide diverse cell behaviours and functions are connected to tight junctions, transmitting information to and from the cytoskeleton, nucleus and different cell adhesion complexes. Recent advances have broadened our understanding of the molecular architecture and cellular functions of tight junctions.
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              Adherens junctions: from molecules to morphogenesis.

              How adhesive interactions between cells generate and maintain animal tissue structure remains one of the most challenging and long-standing questions in cell and developmental biology. Adherens junctions (AJs) and the cadherin-catenin complexes at their core are therefore the subjects of intense research. Recent work has greatly advanced our understanding of the molecular organization of AJs and how cadherin-catenin complexes engage actin, microtubules and the endocytic machinery. As a result, we have gained important insights into the molecular mechanisms of tissue morphogenesis.
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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
                18 August 2017
                Jan-Dec 2017
                : 8
                : 2041731417724640
                Affiliations
                [1 ]Department of Chemical and Biomolecular Engineering, Yonsei University, Seoul, Republic of Korea
                [2 ]Program in Nanoscience and Technology, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, Korea
                [3 ]Advanced Institutes of Convergence Technology, Suwon, Korea
                Author notes
                [*]Won-Gun Koh, Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonsei-Ro, Seodaemoon-Gu, Seoul 120-749, Republic of Korea. Email: wongun@ 123456yonsei.ac.kr
                [*]Kangwon Lee, Program in Nanoscience and Technology, Graduate School of Convergence Science and Technology, Seoul National University, Seoul 16229, Korea. Email: kangwonlee@ 123456snu.ac.kr
                Article
                10.1177_2041731417724640
                10.1177/2041731417724640
                5564857
                29081966
                f2019a1e-ddd9-40f3-8da3-036ceb7084f0
                © The Author(s) 2017

                This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License ( http://www.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 May 2017
                : 16 July 2017
                Categories
                Intelligent Scaffolds for Modulating and Promoting Tissue Regeneration
                Custom metadata
                January-December 2017

                Biomedical engineering
                co-culture,tissue engineering,cellular scaffold,hydrogel,electrospun
                Biomedical engineering
                co-culture, tissue engineering, cellular scaffold, hydrogel, electrospun

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