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3D bioprinting of dynamic hydrogel bioinks enabled by small molecule modulators.
Hull, Sarah M; Lou, Junzhe; Lindsay, Christopher D; Navarro, Renato S; Cai, Betty; Brunel, Lucia G; Westerfield, Ashley D; Xia, Yan; Heilshorn, Sarah C.
Afiliación
  • Hull SM; Department of Chemical Engineering, Stanford University, Stanford, CA, USA.
  • Lou J; Department of Materials Science and Engineering, Stanford University, Stanford, CA, USA.
  • Lindsay CD; Department of Materials Science and Engineering, Stanford University, Stanford, CA, USA.
  • Navarro RS; Department of Materials Science and Engineering, Stanford University, Stanford, CA, USA.
  • Cai B; Department of Materials Science and Engineering, Stanford University, Stanford, CA, USA.
  • Brunel LG; Department of Chemical Engineering, Stanford University, Stanford, CA, USA.
  • Westerfield AD; Department of Bioengineering, Stanford University, Stanford, CA, USA.
  • Xia Y; Department of Chemistry, Stanford University, Stanford, CA, USA.
  • Heilshorn SC; Department of Materials Science and Engineering, Stanford University, Stanford, CA, USA.
Sci Adv ; 9(13): eade7880, 2023 03 31.
Article en En | MEDLINE | ID: mdl-37000873
ABSTRACT
Three-dimensional bioprinting has emerged as a promising tool for spatially patterning cells to fabricate models of human tissue. Here, we present an engineered bioink material designed to have viscoelastic mechanical behavior, similar to that of living tissue. This viscoelastic bioink is cross-linked through dynamic covalent bonds, a reversible bond type that allows for cellular remodeling over time. Viscoelastic materials are challenging to use as inks, as one must tune the kinetics of the dynamic cross-links to allow for both extrudability and long-term stability. We overcome this challenge through the use of small molecule catalysts and competitors that temporarily modulate the cross-linking kinetics and degree of network formation. These inks were then used to print a model of breast cancer cell invasion, where the inclusion of dynamic cross-links was found to be required for the formation of invasive protrusions. Together, we demonstrate the power of engineered, dynamic bioinks to recapitulate the native cellular microenvironment for disease modeling.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Andamios del Tejido / Bioimpresión Límite: Humans Idioma: En Revista: Sci Adv Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Andamios del Tejido / Bioimpresión Límite: Humans Idioma: En Revista: Sci Adv Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos