Tissue geometry drives deterministic organoid patterning

Author:

Gjorevski N.1ORCID,Nikolaev M.1ORCID,Brown T. E.23ORCID,Mitrofanova O.1,Brandenberg N.1ORCID,DelRio F. W.4ORCID,Yavitt F. M.23ORCID,Liberali P.5ORCID,Anseth K. S.23ORCID,Lutolf M. P.16ORCID

Affiliation:

1. Laboratory of Stem Cell Bioengineering, Institute of Bioengineering, School of Life Sciences (SV) and School of Engineering (STI), Ecole Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.

2. Department of Chemical and Biological Engineering, University of Colorado, Boulder, CO 80309, USA.

3. BioFrontiers Institute, University of Colorado, Boulder, CO 80303, USA.

4. Material, Physical, and Chemical Sciences Center, Sandia National Laboratories, Albuquerque, NM 87185, USA.

5. Friedrich Miescher Institute for Biomedical Research (FMI), Basel, Switzerland.

6. Institute of Chemical Sciences and Engineering, School of Basic Science (SB), EPFL, Lausanne, Switzerland.

Abstract

Spatial and temporal organoid control Stem cell–derived organoids form through self-organization and serve as models for organ development, function, and disease, with potential applications in drug development and personalized medicine. However, in the absence of external guidance, developmental processes are stochastic, resulting in variable end products that differ significantly from the native organ. Gjorevski et al . developed approaches for specifying the initial organoid geometry to build intestinal organoids of defined shape, size, and cell distributions, forming structures that are predictable, more similar to normal organs, and reproducible (see the Perspective by Huycke and Gartner). These methods identify symmetry-breaking mechanisms in intestinal morphogenesis and have potential for standardizing organoid-based therapies and facilitating the refinement of mechanistic studies. —BAP

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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