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A 3D Toolbox to Enhance Physiological Relevance of Human Tissue Models

We discuss the current challenges and future prospects of flow-based organoid models and 3D self-assembling scaffolds. The existing paradigm of 3D culture suffers from a lack of control over organoid size and shape; can be an obstacle for cell harvesting and extended cellular and molecular analysis;...

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Bibliographic Details
Published in:Trends in biotechnology (Regular ed.) 2016-09, Vol.34 (9), p.757-769
Main Authors: Picollet-D’hahan, Nathalie, Dolega, Monika E, Liguori, Lavinia, Marquette, Christophe, Le Gac, Séverine, Gidrol, Xavier, Martin, Donald K
Format: Article
Language:English
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Summary:We discuss the current challenges and future prospects of flow-based organoid models and 3D self-assembling scaffolds. The existing paradigm of 3D culture suffers from a lack of control over organoid size and shape; can be an obstacle for cell harvesting and extended cellular and molecular analysis; and does not provide access to the function of exocrine glands. Moreover, existing organ-on-chip models are mostly composed of 2D extracellular matrix (ECM)-coated elastomeric membranes that do not mimic real organ architectures. A new comprehensive 3D toolbox for cell biology has emerged to address some of these issues. Advances in microfabrication and cell-culturing approaches enable the engineering of sophisticated models that mimic organ 3D architectures and physiological conditions, while supporting flow-based drug screening and secretomics-based diagnosis.
ISSN:0167-7799
1879-3096
DOI:10.1016/j.tibtech.2016.06.012