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Electrospinning PCL Scaffolds Manufacture for Three-Dimensional Breast Cancer Cell Culture

In vitro cell culture is traditionally performed within two-dimensional (2D) environments, providing a quick and cheap way to study cell properties in a laboratory. However, 2D systems differ from the in vivo environment and may not mimic the physiological cell behavior realistically. For instance,...

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Autores principales: Rabionet, Marc, Yeste, Marc, Puig, Teresa, Ciurana, Joaquim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418676/
https://www.ncbi.nlm.nih.gov/pubmed/30971005
http://dx.doi.org/10.3390/polym9080328
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author Rabionet, Marc
Yeste, Marc
Puig, Teresa
Ciurana, Joaquim
author_facet Rabionet, Marc
Yeste, Marc
Puig, Teresa
Ciurana, Joaquim
author_sort Rabionet, Marc
collection PubMed
description In vitro cell culture is traditionally performed within two-dimensional (2D) environments, providing a quick and cheap way to study cell properties in a laboratory. However, 2D systems differ from the in vivo environment and may not mimic the physiological cell behavior realistically. For instance, 2D culture models are thought to induce cancer stem cells (CSCs) differentiation, a rare cancer cell subpopulation responsible for tumor initiation and relapse. This fact hinders the development of therapeutic strategies for tumors with a high relapse percentage, such as triple negative breast cancer (TNBC). Thus, three-dimensional (3D) scaffolds have emerged as an attractive alternative to monolayer culture, simulating the extracellular matrix structure and maintaining the differentiation state of cells. In this work, scaffolds were fabricated through electrospinning different poly(ε-caprolactone)-acetone solutions. Poly(ε-caprolactone) (PCL) meshes were seeded with triple negative breast cancer (TNBC) cells and 15% PCL scaffolds displayed significantly (p < 0.05) higher cell proliferation and elongation than the other culture systems. Moreover, cells cultured on PCL scaffolds exhibited higher mammosphere forming capacity and aldehyde dehydrogenase activity than 2D-cultured cells, indicating a breast CSCs enrichment. These results prove the powerful capability of electrospinning technology in terms of poly(ε-caprolactone) nanofibers fabrication. In addition, this study has demonstrated that electrospun 15% PCL scaffolds are suitable tools to culture breast cancer cells in a more physiological way and to expand the niche of breast CSCs. In conclusion, three-dimensional cell culture using PCL scaffolds could be useful to study cancer stem cell behavior and may also trigger the development of new specific targets against such malignant subpopulation.
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spelling pubmed-64186762019-04-02 Electrospinning PCL Scaffolds Manufacture for Three-Dimensional Breast Cancer Cell Culture Rabionet, Marc Yeste, Marc Puig, Teresa Ciurana, Joaquim Polymers (Basel) Article In vitro cell culture is traditionally performed within two-dimensional (2D) environments, providing a quick and cheap way to study cell properties in a laboratory. However, 2D systems differ from the in vivo environment and may not mimic the physiological cell behavior realistically. For instance, 2D culture models are thought to induce cancer stem cells (CSCs) differentiation, a rare cancer cell subpopulation responsible for tumor initiation and relapse. This fact hinders the development of therapeutic strategies for tumors with a high relapse percentage, such as triple negative breast cancer (TNBC). Thus, three-dimensional (3D) scaffolds have emerged as an attractive alternative to monolayer culture, simulating the extracellular matrix structure and maintaining the differentiation state of cells. In this work, scaffolds were fabricated through electrospinning different poly(ε-caprolactone)-acetone solutions. Poly(ε-caprolactone) (PCL) meshes were seeded with triple negative breast cancer (TNBC) cells and 15% PCL scaffolds displayed significantly (p < 0.05) higher cell proliferation and elongation than the other culture systems. Moreover, cells cultured on PCL scaffolds exhibited higher mammosphere forming capacity and aldehyde dehydrogenase activity than 2D-cultured cells, indicating a breast CSCs enrichment. These results prove the powerful capability of electrospinning technology in terms of poly(ε-caprolactone) nanofibers fabrication. In addition, this study has demonstrated that electrospun 15% PCL scaffolds are suitable tools to culture breast cancer cells in a more physiological way and to expand the niche of breast CSCs. In conclusion, three-dimensional cell culture using PCL scaffolds could be useful to study cancer stem cell behavior and may also trigger the development of new specific targets against such malignant subpopulation. MDPI 2017-08-01 /pmc/articles/PMC6418676/ /pubmed/30971005 http://dx.doi.org/10.3390/polym9080328 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rabionet, Marc
Yeste, Marc
Puig, Teresa
Ciurana, Joaquim
Electrospinning PCL Scaffolds Manufacture for Three-Dimensional Breast Cancer Cell Culture
title Electrospinning PCL Scaffolds Manufacture for Three-Dimensional Breast Cancer Cell Culture
title_full Electrospinning PCL Scaffolds Manufacture for Three-Dimensional Breast Cancer Cell Culture
title_fullStr Electrospinning PCL Scaffolds Manufacture for Three-Dimensional Breast Cancer Cell Culture
title_full_unstemmed Electrospinning PCL Scaffolds Manufacture for Three-Dimensional Breast Cancer Cell Culture
title_short Electrospinning PCL Scaffolds Manufacture for Three-Dimensional Breast Cancer Cell Culture
title_sort electrospinning pcl scaffolds manufacture for three-dimensional breast cancer cell culture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6418676/
https://www.ncbi.nlm.nih.gov/pubmed/30971005
http://dx.doi.org/10.3390/polym9080328
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