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      3D bioprinting of methacrylated hyaluronic acid (MeHA) hydrogel with intrinsic osteogenicity

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          Abstract

          In bone regenerative medicine there is a need for suitable bone substitutes. Hydrogels have excellent biocompatible and biodegradable characteristics, but their visco-elastic properties limit their applicability, especially with respect to 3D bioprinting. In this study, we modified the naturally occurring extracellular matrix glycosaminoglycan hyaluronic acid (HA), in order to yield photo-crosslinkable hydrogels with increased mechanical stiffness and long-term stability, and with minimal decrease in cytocompatibility. Application of these tailor-made methacrylated hyaluronic acid (MeHA) gels for bone tissue engineering and 3D bioprinting was the subject of investigation. Visco-elastic properties of MeHA gels, measured by rheology and dynamic mechanical analysis, showed that irradiation of the hydrogels with UV light led to increased storage moduli and elastic moduli, indicating increasing gel rigidity. Subsequently, human bone marrow derived mesenchymal stromal cells (MSCs) were incorporated into MeHA hydrogels, and cell viability remained 64.4% after 21 days of culture. Osteogenic differentiation of MSCs occurred spontaneously in hydrogels with high concentrations of MeHA polymer, in absence of additional osteogenic stimuli. Addition of bone morphogenetic protein-2 (BMP-2) to the culture medium further increased osteogenic differentiation, as evidenced by increased matrix mineralisation. MeHA hydrogels demonstrated to be suitable for 3D bioprinting, and were printed into porous and anatomically shaped scaffolds. Taken together, photosensitive MeHA-based hydrogels fulfilled our criteria for cellular bioprinted bone constructs within a narrow window of concentration.

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          Most cited references34

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          Hydrogels in regenerative medicine.

          Hydrogels, due to their unique biocompatibility, flexible methods of synthesis, range of constituents, and desirable physical characteristics, have been the material of choice for many applications in regenerative medicine. They can serve as scaffolds that provide structural integrity to tissue constructs, control drug and protein delivery to tissues and cultures, and serve as adhesives or barriers between tissue and material surfaces. In this work, the properties of hydrogels that are important for tissue engineering applications and the inherent material design constraints and challenges are discussed. Recent research involving several different hydrogels polymerized from a variety of synthetic and natural monomers using typical and novel synthetic methods are highlighted. Finally, special attention is given to the microfabrication techniques that are currently resulting in important advances in the field.
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            Natural-origin polymers as carriers and scaffolds for biomolecules and cell delivery in tissue engineering applications.

            The present paper intends to overview a wide range of natural-origin polymers with special focus on proteins and polysaccharides (the systems more inspired on the extracellular matrix) that are being used in research, or might be potentially useful as carriers systems for active biomolecules or as cell carriers with application in the tissue engineering field targeting several biological tissues. The combination of both applications into a single material has proven to be very challenging though. The paper presents also some examples of commercially available natural-origin polymers with applications in research or in clinical use in several applications. As it is recognized, this class of polymers is being widely used due to their similarities with the extracellular matrix, high chemical versatility, typically good biological performance and inherent cellular interaction and, also very significant, the cell or enzyme-controlled degradability. These biocharacteristics classify the natural-origin polymers as one of the most attractive options to be used in the tissue engineering field and drug delivery applications.
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              Small functional groups for controlled differentiation of hydrogel-encapsulated human mesenchymal stem cells.

              Cell-matrix interactions have critical roles in regeneration, development and disease. The work presented here demonstrates that encapsulated human mesenchymal stem cells (hMSCs) can be induced to differentiate down osteogenic and adipogenic pathways by controlling their three-dimensional environment using tethered small-molecule chemical functional groups. Hydrogels were formed using sufficiently low concentrations of tether molecules to maintain constant physical characteristics, encapsulation of hMSCs in three dimensions prevented changes in cell morphology, and hMSCs were shown to differentiate in normal growth media, indicating that the small-molecule functional groups induced differentiation. To our knowledge, this is the first example where synthetic matrices are shown to control induction of multiple hMSC lineages purely through interactions with small-molecule chemical functional groups tethered to the hydrogel material. Strategies using simple chemistry to control complex biological processes would be particularly powerful as they could make production of therapeutic materials simpler, cheaper and more easily controlled.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                6 June 2017
                2017
                : 12
                : 6
                : e0177628
                Affiliations
                [1 ]Department of Orthopaedics, University Medical Center Utrecht, Utrecht, the Netherlands
                [2 ]Department of Pharmaceutics, Utrecht Institute for Pharmaceutical Sciences (UIPS), Utrecht University, Utrecht, the Netherlands
                [3 ]Faculty of Veterinary Medicine, Utrecht University, Utrecht, the Netherlands
                Kyoto Daigaku, JAPAN
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                • Conceptualization: MP BG FM CO WD TV JA.

                • Data curation: MP BG MR AA FM CO WD TV JA.

                • Formal analysis: MP BG.

                • Funding acquisition: FM CO WD TV JA.

                • Investigation: MP BG MR AA.

                • Methodology: MP BG MR AA FM CO WD TV JA.

                • Project administration: MP BG JA.

                • Resources: FM CO WD TV JA.

                • Supervision: FM CO WD TV JA.

                • Validation: MP BG JA.

                • Visualization: MP JA.

                • Writing – original draft: MP.

                • Writing – review & editing: MP BG MR AA FM CO WD TV JA.

                Author information
                http://orcid.org/0000-0002-2996-9697
                Article
                PONE-D-16-27336
                10.1371/journal.pone.0177628
                5460858
                28586346
                da41571f-b02b-46f0-a046-7f388dea0466
                © 2017 Poldervaart et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 10 August 2016
                : 1 May 2017
                Page count
                Figures: 6, Tables: 1, Pages: 15
                Funding
                Funded by: Reumafonds (NL)
                Award Recipient :
                Funded by: Biomedical Materials Institute
                Award ID: P2.04 BONE-IP
                Award Recipient :
                MP: This research forms part of the Project P2.04 BONE-IP of the research program of the BioMedical Materials institute, co-funded by the Dutch Ministry of Economic Affairs. Funding sources had no role in study design, data collection and analysis or data interpretation. JA was supported by the Dutch Arthritis Foundation.
                Categories
                Research Article
                Physical Sciences
                Materials Science
                Materials by Structure
                Amorphous Solids
                Gels
                Physical Sciences
                Materials Science
                Materials by Structure
                Mixtures
                Gels
                Biology and life sciences
                Biotechnology
                Bioengineering
                Tissue engineering
                3D bioprinting
                Engineering and technology
                Bioengineering
                Tissue engineering
                3D bioprinting
                Physical Sciences
                Chemistry
                Polymer Chemistry
                Macromolecules
                Polymers
                Physical Sciences
                Materials Science
                Materials by Structure
                Polymers
                Biology and Life Sciences
                Developmental Biology
                Cell Differentiation
                Biology and Life Sciences
                Biotechnology
                Bioengineering
                Tissue Engineering
                Engineering and Technology
                Bioengineering
                Tissue Engineering
                Research and Analysis Methods
                Specimen Preparation and Treatment
                Staining
                Group-Specific Staining
                Alizarin Staining
                Engineering and technology
                Electronics engineering
                3D printing
                Physical Sciences
                Chemistry
                Electrochemistry
                Electrochemical Cells
                Primary Cells
                Custom metadata
                The minimal underlying data sets necessary for replication of the study are available within the manuscript itself.

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                Uncategorized

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