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Consistent and reproducible cultures of large-scale 3D mammary epithelial structures using an accessible bioprinting platform

BACKGROUND: Standard three-dimensional (3D) in vitro culture techniques, such as those used for mammary epithelial cells, rely on random distribution of cells within hydrogels. Although these systems offer advantages over traditional 2D models, limitations persist owing to the lack of control over c...

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Autores principales: Reid, John A., Mollica, Peter M., Bruno, Robert D., Sachs, Patrick C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180647/
https://www.ncbi.nlm.nih.gov/pubmed/30305139
http://dx.doi.org/10.1186/s13058-018-1045-4
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author Reid, John A.
Mollica, Peter M.
Bruno, Robert D.
Sachs, Patrick C.
author_facet Reid, John A.
Mollica, Peter M.
Bruno, Robert D.
Sachs, Patrick C.
author_sort Reid, John A.
collection PubMed
description BACKGROUND: Standard three-dimensional (3D) in vitro culture techniques, such as those used for mammary epithelial cells, rely on random distribution of cells within hydrogels. Although these systems offer advantages over traditional 2D models, limitations persist owing to the lack of control over cellular placement within the hydrogel. This results in experimental inconsistencies and random organoid morphology. Robust, high-throughput experimentation requires greater standardization of 3D epithelial culture techniques. METHODS: Here, we detail the use of a 3D bioprinting platform as an investigative tool to control the 3D formation of organoids through the “self-assembly” of human mammary epithelial cells. Experimental bioprinting procedures were optimized to enable the formation of controlled arrays of individual mammary organoids. We define the distance and cell number parameters necessary to print individual organoids that do not interact between print locations as well as those required to generate large contiguous organoids connected through multiple print locations. RESULTS: We demonstrate that as few as 10 cells can be used to form 3D mammary structures in a single print and that prints up to 500 μm apart can fuse to form single large structures. Using these fusion parameters, we demonstrate that both linear and non-linear (contiguous circles) can be generated with sizes of 3 mm in length/diameter. We confirm that cells from individual prints interact to form structures with a contiguous lumen. Finally, we demonstrate that organoids can be printed into human collagen hydrogels, allowing for all-human 3D culture systems. CONCLUSIONS: Our platform is adaptable to different culturing protocols and is superior to traditional random 3D culture techniques in efficiency, reproducibility, and scalability. Importantly, owing to the low-cost accessibility and computer numerical control–driven platform of our 3D bioprinter, we have the ability to disseminate our experiments with absolute precision to interested laboratories. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13058-018-1045-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-61806472018-10-18 Consistent and reproducible cultures of large-scale 3D mammary epithelial structures using an accessible bioprinting platform Reid, John A. Mollica, Peter M. Bruno, Robert D. Sachs, Patrick C. Breast Cancer Res Research Article BACKGROUND: Standard three-dimensional (3D) in vitro culture techniques, such as those used for mammary epithelial cells, rely on random distribution of cells within hydrogels. Although these systems offer advantages over traditional 2D models, limitations persist owing to the lack of control over cellular placement within the hydrogel. This results in experimental inconsistencies and random organoid morphology. Robust, high-throughput experimentation requires greater standardization of 3D epithelial culture techniques. METHODS: Here, we detail the use of a 3D bioprinting platform as an investigative tool to control the 3D formation of organoids through the “self-assembly” of human mammary epithelial cells. Experimental bioprinting procedures were optimized to enable the formation of controlled arrays of individual mammary organoids. We define the distance and cell number parameters necessary to print individual organoids that do not interact between print locations as well as those required to generate large contiguous organoids connected through multiple print locations. RESULTS: We demonstrate that as few as 10 cells can be used to form 3D mammary structures in a single print and that prints up to 500 μm apart can fuse to form single large structures. Using these fusion parameters, we demonstrate that both linear and non-linear (contiguous circles) can be generated with sizes of 3 mm in length/diameter. We confirm that cells from individual prints interact to form structures with a contiguous lumen. Finally, we demonstrate that organoids can be printed into human collagen hydrogels, allowing for all-human 3D culture systems. CONCLUSIONS: Our platform is adaptable to different culturing protocols and is superior to traditional random 3D culture techniques in efficiency, reproducibility, and scalability. Importantly, owing to the low-cost accessibility and computer numerical control–driven platform of our 3D bioprinter, we have the ability to disseminate our experiments with absolute precision to interested laboratories. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13058-018-1045-4) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-10 2018 /pmc/articles/PMC6180647/ /pubmed/30305139 http://dx.doi.org/10.1186/s13058-018-1045-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Reid, John A.
Mollica, Peter M.
Bruno, Robert D.
Sachs, Patrick C.
Consistent and reproducible cultures of large-scale 3D mammary epithelial structures using an accessible bioprinting platform
title Consistent and reproducible cultures of large-scale 3D mammary epithelial structures using an accessible bioprinting platform
title_full Consistent and reproducible cultures of large-scale 3D mammary epithelial structures using an accessible bioprinting platform
title_fullStr Consistent and reproducible cultures of large-scale 3D mammary epithelial structures using an accessible bioprinting platform
title_full_unstemmed Consistent and reproducible cultures of large-scale 3D mammary epithelial structures using an accessible bioprinting platform
title_short Consistent and reproducible cultures of large-scale 3D mammary epithelial structures using an accessible bioprinting platform
title_sort consistent and reproducible cultures of large-scale 3d mammary epithelial structures using an accessible bioprinting platform
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180647/
https://www.ncbi.nlm.nih.gov/pubmed/30305139
http://dx.doi.org/10.1186/s13058-018-1045-4
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