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      Sliding Hydrogels with Mobile Molecular Ligands and Crosslinks as 3D Stem Cell Niche

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      Advanced Materials
      Wiley-Blackwell

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          Abstract

          <p class="first" id="P1">Here we report the development of sliding hydrogel with mobile crosslinks and biochemical ligands as a 3D stem cell niche. The molecular mobility of this sliding hydrogel allows stem cells to reorganize the surrounding ligands and change their morphology in 3D. Without changing matrix stiffness, sliding hydrogels support efficient stem cell differentiation toward multiple lineages including adipogenesis, chondrogenesis and osteogenesis. </p><p id="P2"> <div class="figure-container so-text-align-c"> <img alt="" class="figure" src="/document_file/3b0b1167-9f2a-4f40-8368-a3b7f9e9ff87/PubMedCentral/image/nihms-807392-f0001.jpg"/> </div> </p>

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          Most cited references20

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          Photodegradable hydrogels for dynamic tuning of physical and chemical properties.

          We report a strategy to create photodegradable poly(ethylene glycol)-based hydrogels through rapid polymerization of cytocompatible macromers for remote manipulation of gel properties in situ. Postgelation control of the gel properties was demonstrated to introduce temporal changes, creation of arbitrarily shaped features, and on-demand pendant functionality release. Channels photodegraded within a hydrogel containing encapsulated cells allow cell migration. Temporal variation of the biochemical gel composition was used to influence chondrogenic differentiation of encapsulated stem cells. Photodegradable gels that allow real-time manipulation of material properties or chemistry provide dynamic environments with the scope to answer fundamental questions about material regulation of live cell function and may affect an array of applications from design of drug delivery vehicles to tissue engineering systems.
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            Degradation-mediated cellular traction directs stem cell fate in covalently crosslinked three-dimensional hydrogels

            Although cell-matrix adhesive interactions are known to regulate stem cell differentiation, the underlying mechanisms, in particular for direct three-dimensional (3D) encapsulation within hydrogels, are poorly understood. Here, we demonstrate that in covalently crosslinked hyaluronic acid (HA) hydrogels, the differentiation of human mesenchymal stem cells (hMSCs) is directed by the generation of degradation-mediated cellular-traction, independent of cell morphology or matrix mechanics. hMSCs within HA hydrogels of equivalent elastic moduli that either permit (restrict) cell-mediated degradation exhibited high (low) degrees of cell spreading and high (low) tractions, and favoured osteogenesis (adipogenesis). In addition, switching the permissive hydrogel to a restrictive state via delayed secondary crosslinking reduced further hydrogel degradation, suppressed traction, and caused a switch from osteogenesis to adipogenesis in the absence of changes to the extended cellular morphology. Also, inhibiting tension-mediated signalling in the permissive environment mirrored the effects of delayed secondary crosslinking, whereas upregulating tension induced osteogenesis even in the restrictive environment.
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              The Polyrotaxane Gel: A Topological Gel by Figure-of-Eight Cross-links

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                Author and article information

                Journal
                Advanced Materials
                Adv. Mater.
                Wiley-Blackwell
                09359648
                September 2016
                September 2016
                : 28
                : 33
                : 7257-7263
                Article
                10.1002/adma.201601484
                5127628
                27305637
                c3b7f53e-deb1-4a7e-a5ff-b08c53f2fb50
                © 2016

                http://doi.wiley.com/10.1002/tdm_license_1.1

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