3D bioprinting of dynamic hydrogel bioinks enabled by small molecule modulators

Author:

Hull Sarah M.1ORCID,Lou Junzhe2ORCID,Lindsay Christopher D.2,Navarro Renato S.2ORCID,Cai Betty2,Brunel Lucia G.1ORCID,Westerfield Ashley D.3ORCID,Xia Yan4ORCID,Heilshorn Sarah C.2ORCID

Affiliation:

1. Department of Chemical Engineering, Stanford University, Stanford, CA, USA.

2. Department of Materials Science and Engineering, Stanford University, Stanford, CA, USA.

3. Department of Bioengineering, Stanford University, Stanford, CA, USA.

4. Department of Chemistry, Stanford University, Stanford, CA, USA.

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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