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Inherent aggressive character of invasive and non-invasive cells dictates the in vitro migration pattern of multicellular spheroid

Cellular migration, a process relevant to metastasis, is mostly studied in the conventional 2D condition. However, cells cultured in the 3D condition assumed to mimic the in vivo conditions better. The current study is designed to compare an invasive and non-invasive adenocarcinoma cell with an inva...

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Autores principales: Gayan, Sukanya, Teli, Abhishek, Dey, Tuli
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599661/
https://www.ncbi.nlm.nih.gov/pubmed/28912559
http://dx.doi.org/10.1038/s41598-017-10078-7
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author Gayan, Sukanya
Teli, Abhishek
Dey, Tuli
author_facet Gayan, Sukanya
Teli, Abhishek
Dey, Tuli
author_sort Gayan, Sukanya
collection PubMed
description Cellular migration, a process relevant to metastasis, is mostly studied in the conventional 2D condition. However, cells cultured in the 3D condition assumed to mimic the in vivo conditions better. The current study is designed to compare an invasive and non-invasive adenocarcinoma cell with an invasive fibrosarcoma cell to understand the migration pattern of the multicellular spheroid. It is observed that conventional haplotaxis, chemotactic and pseudo-3D migration assay cannot distinguish between the invasive and non-invasive cells conclusively under 2D condition. Invasive spheroids migrate rapidly in sprouting assay in comparison to non-invasive spheroids. Effects of cytochalasin B, marimastat and blebbistatin are tested to determine the influence of different migration modality namely actin polymerization, matrix metalloprotease and acto-myosin in both culture conditions. Altered mRNA profile of cellular migration related genes (FAK, Talin, Paxillin, p130cas and Vinculin) is observed between 2D and 3D condition followed by the changed expression of matrix metallo proteases. A distinct difference is observed in distribution and formation of focal adhesion complex under these culture conditions. This study demonstrates the efficacy of multicellular spheroids in identifying the intrinsic aggressive behavior of different cell lines as a proof of concept and recognizes the potential of spheroids as a migration model.
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spelling pubmed-55996612017-09-19 Inherent aggressive character of invasive and non-invasive cells dictates the in vitro migration pattern of multicellular spheroid Gayan, Sukanya Teli, Abhishek Dey, Tuli Sci Rep Article Cellular migration, a process relevant to metastasis, is mostly studied in the conventional 2D condition. However, cells cultured in the 3D condition assumed to mimic the in vivo conditions better. The current study is designed to compare an invasive and non-invasive adenocarcinoma cell with an invasive fibrosarcoma cell to understand the migration pattern of the multicellular spheroid. It is observed that conventional haplotaxis, chemotactic and pseudo-3D migration assay cannot distinguish between the invasive and non-invasive cells conclusively under 2D condition. Invasive spheroids migrate rapidly in sprouting assay in comparison to non-invasive spheroids. Effects of cytochalasin B, marimastat and blebbistatin are tested to determine the influence of different migration modality namely actin polymerization, matrix metalloprotease and acto-myosin in both culture conditions. Altered mRNA profile of cellular migration related genes (FAK, Talin, Paxillin, p130cas and Vinculin) is observed between 2D and 3D condition followed by the changed expression of matrix metallo proteases. A distinct difference is observed in distribution and formation of focal adhesion complex under these culture conditions. This study demonstrates the efficacy of multicellular spheroids in identifying the intrinsic aggressive behavior of different cell lines as a proof of concept and recognizes the potential of spheroids as a migration model. Nature Publishing Group UK 2017-09-14 /pmc/articles/PMC5599661/ /pubmed/28912559 http://dx.doi.org/10.1038/s41598-017-10078-7 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gayan, Sukanya
Teli, Abhishek
Dey, Tuli
Inherent aggressive character of invasive and non-invasive cells dictates the in vitro migration pattern of multicellular spheroid
title Inherent aggressive character of invasive and non-invasive cells dictates the in vitro migration pattern of multicellular spheroid
title_full Inherent aggressive character of invasive and non-invasive cells dictates the in vitro migration pattern of multicellular spheroid
title_fullStr Inherent aggressive character of invasive and non-invasive cells dictates the in vitro migration pattern of multicellular spheroid
title_full_unstemmed Inherent aggressive character of invasive and non-invasive cells dictates the in vitro migration pattern of multicellular spheroid
title_short Inherent aggressive character of invasive and non-invasive cells dictates the in vitro migration pattern of multicellular spheroid
title_sort inherent aggressive character of invasive and non-invasive cells dictates the in vitro migration pattern of multicellular spheroid
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5599661/
https://www.ncbi.nlm.nih.gov/pubmed/28912559
http://dx.doi.org/10.1038/s41598-017-10078-7
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