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Self-organization of organoids from endoderm-derived cells.

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Lewis,  Allison
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Keshara,  Rashmiparvathi
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Kim,  Yung Hae
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Grapin-Botton,  Anne
Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society;

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Citation

Lewis, A., Keshara, R., Kim, Y. H., & Grapin-Botton, A. (2020). Self-organization of organoids from endoderm-derived cells. Journal of molecular medicine (Berlin, Germany), 99(4), 449-462. doi:10.1007/s00109-020-02010-w.


Cite as: https://hdl.handle.net/21.11116/0000-0008-A346-1
Abstract
Organoids constitute biological systems which are used to model organ development, homeostasis, regeneration, and disease in vitro and hold promise for use in therapy. Reflecting in vivo development, organoids form from tissue cells or pluripotent stem cells. Cues provided from the media and individual cells promote self-organization of these uniform starting cells into a structure, with emergent differentiated cells, morphology, and often functionality that resemble the tissue of origin. Therefore, organoids provide a complement to two-dimensional in vitro culture and in vivo animal models of development, providing the experimental control and flexibility of in vitro methods with the three-dimensional context of in vivo models, with fewer ethical restraints than human or animal work. However, using organoids, we are only just beginning to understand on the cellular level how the external conditions and signaling between individual cells promote the emergence of cells and structures. In this review, we focus specifically on organoids derived from endodermal tissues: the starting conditions of the cells, signaling mechanisms, and external media that allow the emergence of higher order self-organization.