Abstract

AbstractLocalization of multiple hydrogels is expected to develop the structure of 3D tissue models in a location‐specific manner. Here, 3D tissue morphogenesis is spatially guided by localizing different hydrogel conditions at different parts of a tissue. To achieve the localization, a unit‐based scaffold is developed with a unique frame design to trap hydrogel solutions inside their designated units. An optimal range of unit dimensions and surface wettabilities enables a solution trapping up to several cubic millimeters without any need for chemical additives. This capability allows spatial organization of biomolecular compositions and physical conditions of hydrogels, as well as the relative position of biological samples (cells, spheroids, and reconstituted tissues) within the scaffold. Successful localization of branching development on reconstituted human epithelial tissues is achieved by localizing growth factors or cross‐linked matrix proteins within hydrogels, demonstrating a direct dependence on local hydrogel conditions. Unlike 3D‐bioprinting or microfluidic techniques, this scaffold‐based localization of hydrogels requires only a manual pipetting and no specialized tools, making it ready‐to‐use for researchers from any field. This localization technique provides a new promising route to spatially control morphogenesis, differentiation, and other developmental processes within 3D organoids or tissue models for practical biomedical applications in the future.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call