Search for authorsSearch for similar articles
33
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      Latest Advances in Cryogel Technology for Biomedical Applications

      Read this article at

      ScienceOpenPublisher
      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.

          Related collections

          Most cited references427

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          Ror2 signaling regulates Golgi structure and transport through IFT20 for tumor invasiveness

          Signaling through the Ror2 receptor tyrosine kinase promotes invadopodia formation for tumor invasion. Here, we identify intraflagellar transport 20 (IFT20) as a new target of this signaling in tumors that lack primary cilia, and find that IFT20 mediates the ability of Ror2 signaling to induce the invasiveness of these tumors. We also find that IFT20 regulates the nucleation of Golgi-derived microtubules by affecting the GM130-AKAP450 complex, which promotes Golgi ribbon formation in achieving polarized secretion for cell migration and invasion. Furthermore, IFT20 promotes the efficiency of transport through the Golgi complex. These findings shed new insights into how Ror2 signaling promotes tumor invasiveness, and also advance the understanding of how Golgi structure and transport can be regulated.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Matrix elasticity directs stem cell lineage specification.

            Microenvironments appear important in stem cell lineage specification but can be difficult to adequately characterize or control with soft tissues. Naive mesenchymal stem cells (MSCs) are shown here to specify lineage and commit to phenotypes with extreme sensitivity to tissue-level elasticity. Soft matrices that mimic brain are neurogenic, stiffer matrices that mimic muscle are myogenic, and comparatively rigid matrices that mimic collagenous bone prove osteogenic. During the initial week in culture, reprogramming of these lineages is possible with addition of soluble induction factors, but after several weeks in culture, the cells commit to the lineage specified by matrix elasticity, consistent with the elasticity-insensitive commitment of differentiated cell types. Inhibition of nonmuscle myosin II blocks all elasticity-directed lineage specification-without strongly perturbing many other aspects of cell function and shape. The results have significant implications for understanding physical effects of the in vivo microenvironment and also for therapeutic uses of stem cells.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              Hydrogel: Preparation, characterization, and applications: A review

              Graphical abstract
                Bookmark

                Author and article information

                Contributors
                (View ORCID Profile)
                Journal
                Advanced Therapeutics
                Adv. Therap.
                Wiley
                2366-3987
                2366-3987
                February 10 2019
                April 2019
                February 10 2019
                April 2019
                : 2
                : 4
                : 1800114
                Affiliations
                [1 ]Center of NanotechnologyKing Abdulaziz University Jeddah 21589 Saudi Arabia
                [2 ]Center for Biomedical EngineeringDepartment of MedicineBrigham and Women's HospitalHarvard Medical School Cambridge MA 02139 USA
                [3 ]Department of Chemical EngineeringNortheastern University Boston MA 02115 USA
                [4 ]Department of Tumor ImmunologyOncode Institute, Radboud Institute for Molecular Life SciencesRadboud University Medical Center Nijmegen 6500 The Netherlands
                [5 ]Department of Pharmaceutical SciencesNortheastern University Boston MA 02115 USA
                [6 ]Department of BioengineeringNortheastern University Boston MA 02115 USA
                [7 ]Harvard John A. Paulson School of Engineering and Applied SciencesHarvard University Cambridge MA 02138 USA
                [8 ]Sorbonne UniversityUTC CNRS UMR 7338Biomechanics and Bioengineering (BMBI)University of Technology of Compiègne Compiègne 60159 France
                Article
                10.1002/adtp.201800114
                3c1af88c-1896-467d-b46f-3f356c3db8e0
                © 2019

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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

                History

                Comments

                Comment on this article