Project C2.2 aims to expand the understanding of how the 3D microenvironment, particularly biochemical cues and contractile intracellular forces, influences differentiation into brain, intestinal, and other organoids.
Locally tunable 3D architectures are key to achieving precise and dynamic control of organoid development, utilizing stimulus-responsive materials. These architectures will be employed alongside 3D-printed microfluidics at micrometer precision. Our strategy will advance material-controlled structural and functional organoid development, opening possibilities such as using organoids to study metastasis and other complex biological processes.
Jasmin Aghassi-Hagmann
Karlsruhe Institute of Technology (KIT)
Martin Bastmeyer
Karlsruhe Institute of Technology
Michael Boutros
Heidelberg University
Daniela Duarte Campos
Heidelberg University
Kerstin Göpfrich
Heidelberg University
Simone Mayer
Karlsruhe Institute of Technology (KIT)
Ulrich Schwarz
Heidelberg University
Christine Selhuber-Unkel
Heidelberg University
Joachim Wittbrodt
Heidelberg University