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Wafer-Scale Patterning of Protein Templates for Hydrogel Fabrication.
Kim, Anna A; Castillo, Erica A; Lane, Kerry V; Torres, Gabriela V; Chirikian, Orlando; Wilson, Robin E; Lance, Sydney A; Pardon, Gaspard; Pruitt, Beth L.
Afiliación
  • Kim AA; Department of Materials Science and Engineering, Uppsala University, 751 03 Uppsala, Sweden.
  • Castillo EA; Department of Mechanical Engineering, University of California, Santa Barbara, CA 93106, USA.
  • Lane KV; Department of Mechanical Engineering, University of California, Santa Barbara, CA 93106, USA.
  • Torres GV; Department of Mechanical Engineering, Stanford University, Stanford, CA 94305, USA.
  • Chirikian O; Department of Mechanical Engineering, University of California, Santa Barbara, CA 93106, USA.
  • Wilson RE; Department of Mechanical Engineering, University of California, Santa Barbara, CA 93106, USA.
  • Lance SA; Biomolecular Science and Engineering Program, University of California, Santa Barbara, CA 93106, USA.
  • Pardon G; Department of Mechanical Engineering, Stanford University, Stanford, CA 94305, USA.
  • Pruitt BL; Department of Mechanical Engineering, Stanford University, Stanford, CA 94305, USA.
Micromachines (Basel) ; 12(11)2021 Nov 12.
Article en En | MEDLINE | ID: mdl-34832798
Human-induced pluripotent stem cell-derived cardiomyocytes are a potentially unlimited cell source and promising patient-specific in vitro model of cardiac diseases. Yet, these cells are limited by immaturity and population heterogeneity. Current in vitro studies aiming at better understanding of the mechanical and chemical cues in the microenvironment that drive cellular maturation involve deformable materials and precise manipulation of the microenvironment with, for example, micropatterns. Such microenvironment manipulation most often involves microfabrication protocols which are time-consuming, require cleanroom facilities and photolithography expertise. Here, we present a method to increase the scale of the fabrication pipeline, thereby enabling large-batch generation of shelf-stable microenvironment protein templates on glass chips. This decreases fabrication time and allows for more flexibility in the subsequent steps, for example, in tuning the material properties and the selection of extracellular matrix or cell proteins. Further, the fabrication of deformable hydrogels has been optimized for compatibility with these templates, in addition to the templates being able to be used to acquire protein patterns directly on the glass chips. With our approach, we have successfully controlled the shapes of cardiomyocytes seeded on Matrigel-patterned hydrogels.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Micromachines (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Suecia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Micromachines (Basel) Año: 2021 Tipo del documento: Article País de afiliación: Suecia