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      Applications of Human Amniotic Membrane for Tissue Engineering

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          Abstract

          An important component of tissue engineering (TE) is the supporting matrix upon which cells and tissues grow, also known as the scaffold. Scaffolds must easily integrate with host tissue and provide an excellent environment for cell growth and differentiation. Human amniotic membrane (hAM) is considered as a surgical waste without ethical issue, so it is a highly abundant, cost-effective, and readily available biomaterial. It has biocompatibility, low immunogenicity, adequate mechanical properties (permeability, stability, elasticity, flexibility, resorbability), and good cell adhesion. It exerts anti-inflammatory, antifibrotic, and antimutagenic properties and pain-relieving effects. It is also a source of growth factors, cytokines, and hAM cells with stem cell properties. This important source for scaffolding material has been widely studied and used in various areas of tissue repair: corneal repair, chronic wound treatment, genital reconstruction, tendon repair, microvascular reconstruction, nerve repair, and intraoral reconstruction. Depending on the targeted application, hAM has been used as a simple scaffold or seeded with various types of cells that are able to grow and differentiate. Thus, this natural biomaterial offers a wide range of applications in TE applications. Here, we review hAM properties as a biocompatible and degradable scaffold. Its use strategies (i.e., alone or combined with cells, cell seeding) and its degradation rate are also presented.

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          Tissue engineering

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            Biomaterials & scaffolds for tissue engineering

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              Concise review: isolation and characterization of cells from human term placenta: outcome of the first international Workshop on Placenta Derived Stem Cells.

              Placental tissue draws great interest as a source of cells for regenerative medicine because of the phenotypic plasticity of many of the cell types isolated from this tissue. Furthermore, placenta, which is involved in maintaining fetal tolerance, contains cells that display immunomodulatory properties. These two features could prove useful for future cell therapy-based clinical applications. Placental tissue is readily available and easily procured without invasive procedures, and its use does not elicit ethical debate. Numerous reports describing stem cells from different parts of the placenta, using nearly as numerous isolation and characterization procedures, have been published. Considering the complexity of the placenta, an urgent need exists to define, as clearly as possible, the region of origin and methods of isolation of cells derived from this tissue. On March 23-24, 2007, the first international Workshop on Placenta Derived Stem Cells was held in Brescia, Italy. Most of the research published in this area focuses on mesenchymal stromal cells isolated from various parts of the placenta or epithelial cells isolated from amniotic membrane. The aim of this review is to summarize and provide the state of the art of research in this field, addressing aspects such as cell isolation protocols and characteristics of these cells, as well as providing preliminary indications of the possibilities for use of these cells in future clinical applications.
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                Author and article information

                Contributors
                Role: Academic Editor
                Role: Academic Editor
                Role: Academic Editor
                Role: Academic Editor
                Role: Academic Editor
                Journal
                Membranes (Basel)
                Membranes (Basel)
                membranes
                Membranes
                MDPI
                2077-0375
                25 May 2021
                June 2021
                : 11
                : 6
                : 387
                Affiliations
                [1 ]Université de Bordeaux, INSERM, BIOTIS, U1026, F-33000 Bordeaux, France; mathilde.fenelon@ 123456u-bordeaux.fr (M.F.); sylvain.catros@ 123456u-bordeaux.fr (S.C.); jean-christophe.fricain@ 123456inserm.fr (J.-C.F.)
                [2 ]Service de Chirurgie Orale, CHU Bordeaux, F-33076 Bordeaux, France
                [3 ]Laboratoire de Nanomédecine, Imagerie, Thérapeutique EA 4662, Université Bourgogne Franche-Comté, F-25000 Besançon, France; c3meyer@ 123456chu-besancon.fr (C.M.); laurentobert@ 123456yahoo.fr (L.O.); fauber@ 123456chu-besancon.fr (F.A.)
                [4 ]Service de Chirurgie Maxillo-Faciale, Stomatologie et Odontologie Hospitalière, CHU Besançon, F-25000 Besançon, France; alouvrier@ 123456chu-besancon.fr
                [5 ]Service de Chirurgie Orthopédique, Traumatologique et Plastique, CHU Besançon, F-25000 Besançon, France
                [6 ]Service de Chirurgie Pédiatrique, CHU Besançon, F-25000 Besançon, France
                [7 ]Inserm CIC 1431, CHU Besançon, F-25000 Besançon, France
                [8 ]Université Bourgogne Franche-Comté, INSERM, EFS BFC, UMR1098, Interactions Hôte-Greffon-Tumeur/Ingénierie Cellulaire et Génique, LabEx LipSTIC, F-25000 Besançon, France
                Author notes
                Author information
                https://orcid.org/0000-0002-3419-3467
                Article
                membranes-11-00387
                10.3390/membranes11060387
                8227127
                34070582
                4f64c273-f7ad-4182-8219-17a684f515e9
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 10 April 2021
                : 20 May 2021
                Categories
                Review

                amniotic membrane,cells,biological scaffold,tissue engineering,repair,reconstruction

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