9
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Liver tissue engineering: From implantable tissue to whole organ engineering

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          The term “liver tissue engineering” summarizes one of the ultimate goals of modern biotechnology: the possibility of reproducing in total or in part the functions of the liver in order to treat acute or chronic liver disorders and, ultimately, create a fully functional organ to be transplanted or used as an extracorporeal device. All the technical approaches in the area of liver tissue engineering are based on allocating adult hepatocytes or stem cell‐derived hepatocyte‐like cells within a three‐dimensional structure able to ensure their survival and to maintain their functional phenotype. The hosting structure can be a construct in which hepatocytes are embedded in alginate and/or gelatin or are seeded in a pre‐arranged scaffold made with different types of biomaterials. According to a more advanced methodology termed three‐dimensional bioprinting, hepatocytes are mixed with a bio‐ink and the mixture is printed in different forms, such as tissue‐like layers or spheroids. In the last decade, efforts to engineer a cell microenvironment recapitulating the dynamic native extracellular matrix have become increasingly successful, leading to the hope of satisfying the clinical demand for tissue (or organ) repair and replacement within a reasonable timeframe. Indeed, the preclinical work performed in recent years has shown promising results, and the advancement in the biotechnology of bioreactors, ex vivo perfusion machines, and cell expansion systems associated with a better understanding of liver development and the extracellular matrix microenvironment will facilitate and expedite the translation to technical applications. ( Hepatology Communications 2018;2:131–141)

          Related collections

          Most cited references59

          • Record: found
          • Abstract: found
          • Article: not found

          Alternative projections of mortality and disability by cause 1990–2020: Global Burden of Disease Study

          The Lancet, 349(9064), 1498-1504
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Size- and shape-dependent foreign body immune response to materials implanted in rodents and non-human primates

            The efficacy of implanted biomedical devices is often compromised by host recognition and subsequent foreign body responses. Here, we demonstrate the role of the geometry of implanted materials on their biocompatibility in vivo. In rodent and non-human primate animal models, implanted spheres 1.5 mm and above in diameter across a broad spectrum of materials, including hydrogels, ceramics, metals, and plastics, significantly abrogated foreign body reactions and fibrosis when compared to smaller spheres. We also show that for encapsulated rat pancreatic islet cells transplanted into streptozotocin-treated diabetic C57BL/6 mice, islets prepared in 1.5 mm alginate capsules were able to restore blood-glucose control for up to 180 days, a period more than 5-fold longer than for transplanted grafts encapsulated within conventionally sized 0.5-mm alginate capsules. Our findings suggest that the in vivo biocompatibility of biomedical devices can be significantly improved by simply tuning their spherical dimensions.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Engineering Complex Tissues

                Bookmark

                Author and article information

                Contributors
                m.pinzani@ucl.ac.uk
                Journal
                Hepatol Commun
                Hepatol Commun
                10.1002/(ISSN)2471-254X
                HEP4
                Hepatology Communications
                John Wiley and Sons Inc. (Hoboken )
                2471-254X
                21 December 2017
                February 2018
                : 2
                : 2 ( doiID: 10.1002/hep4.v2.2 )
                : 131-141
                Affiliations
                [ 1 ] University College London, Division of Medicine, Institute for Liver and Digestive Health Royal Free Hospital London United Kingdom
                Author notes
                [*] [* ] ADDRESS CORRESPONDENCE AND REPRINT REQUESTS TO:

                Massimo Pinzani, M.D., Ph.D.

                Royal Free Hospital & University College London

                Institute for Liver and Digestive Health, Division of Medicine

                Rowland Hill Street

                London, NW3 2PF, United Kingdom

                E‐mail: m.pinzani@ 123456ucl.ac.uk

                Tel: +44‐0207‐4332850

                Article
                HEP41136
                10.1002/hep4.1136
                5796330
                29404520
                a686e0bb-2451-42e2-bac6-2834441b14c9
                © 2017 The Authors. Hepatology Communications published by Wiley Periodicals, Inc., on behalf of the American Association for the Study of Liver Diseases.

                This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 02 September 2017
                : 22 October 2017
                : 02 November 2017
                Page count
                Figures: 2, Tables: 1, Pages: 11, Words: 6971
                Funding
                Funded by: University College London Biomedical Research Centre
                Funded by: The Royal Free Charity
                Funded by: The Fiorina Foundation
                Funded by: Royal Free Peter Samuel Award
                Funded by: Innovate UK
                Funded by: National Institute for Health Research
                Award ID: 2017‐2019
                Funded by: Royal Free Charity
                Categories
                Review Article
                Review Articles
                Custom metadata
                2.0
                hep41136
                February 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.3.2.2 mode:remove_FC converted:02.02.2018

                Comments

                Comment on this article