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Understanding flow dynamics, viability and metastatic potency of cervical cancer (HeLa) cells through constricted microchannel

To understand the burgeoning challenges of metastasis, a microchannel of 35 μm diameter, constricted to 7 μm for a distance of 200 μm in a total length of 3 mm, was designed and fabricated using a mask aligner made of polydimethylsiloxane (PDMS) to mimic in vivo capillaries. A thin glass cover-slide...

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Autores principales: Nath, Binita, Raza, Asif, Sethi, Vishal, Dalal, Amaresh, Ghosh, Siddhartha Sankar, Biswas, Gautam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255798/
https://www.ncbi.nlm.nih.gov/pubmed/30478455
http://dx.doi.org/10.1038/s41598-018-35646-3
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author Nath, Binita
Raza, Asif
Sethi, Vishal
Dalal, Amaresh
Ghosh, Siddhartha Sankar
Biswas, Gautam
author_facet Nath, Binita
Raza, Asif
Sethi, Vishal
Dalal, Amaresh
Ghosh, Siddhartha Sankar
Biswas, Gautam
author_sort Nath, Binita
collection PubMed
description To understand the burgeoning challenges of metastasis, a microchannel of 35 μm diameter, constricted to 7 μm for a distance of 200 μm in a total length of 3 mm, was designed and fabricated using a mask aligner made of polydimethylsiloxane (PDMS) to mimic in vivo capillaries. A thin glass cover-slide was mounted on top to monitor the motion of single or aggregated malignant HeLa cells (size 17–30 μm) microscopically through the constricted microchannel at a constant flow rate of 30 μl/h. Quantitative deconvolution of high-speed videographs of a single cell of 30 μm revealed cellular deformation while passing through constriction, having elongation index, average transit velocity and entry time of 2.67, 18 mm/s and 5.1 ms, respectively. Morphological analysis of live and apoptotic cells by dual staining with Acridine Orange/Ethidium Bromide demonstrated retention of a significant viable cell population after exit through the constriction and a viability index of 50% was quantified by dye exclusion assay. The cumulative data for microfluidic parameters, morphology and relevant metastatic MMP2 gene expression efficiency measured by real-time polymerase chain reaction revealed retention of virulence potency that could possibly cause metastasis, would be beneficial in developing futuristic MEMS device for cancer theranostics.
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spelling pubmed-62557982018-12-03 Understanding flow dynamics, viability and metastatic potency of cervical cancer (HeLa) cells through constricted microchannel Nath, Binita Raza, Asif Sethi, Vishal Dalal, Amaresh Ghosh, Siddhartha Sankar Biswas, Gautam Sci Rep Article To understand the burgeoning challenges of metastasis, a microchannel of 35 μm diameter, constricted to 7 μm for a distance of 200 μm in a total length of 3 mm, was designed and fabricated using a mask aligner made of polydimethylsiloxane (PDMS) to mimic in vivo capillaries. A thin glass cover-slide was mounted on top to monitor the motion of single or aggregated malignant HeLa cells (size 17–30 μm) microscopically through the constricted microchannel at a constant flow rate of 30 μl/h. Quantitative deconvolution of high-speed videographs of a single cell of 30 μm revealed cellular deformation while passing through constriction, having elongation index, average transit velocity and entry time of 2.67, 18 mm/s and 5.1 ms, respectively. Morphological analysis of live and apoptotic cells by dual staining with Acridine Orange/Ethidium Bromide demonstrated retention of a significant viable cell population after exit through the constriction and a viability index of 50% was quantified by dye exclusion assay. The cumulative data for microfluidic parameters, morphology and relevant metastatic MMP2 gene expression efficiency measured by real-time polymerase chain reaction revealed retention of virulence potency that could possibly cause metastasis, would be beneficial in developing futuristic MEMS device for cancer theranostics. Nature Publishing Group UK 2018-11-26 /pmc/articles/PMC6255798/ /pubmed/30478455 http://dx.doi.org/10.1038/s41598-018-35646-3 Text en © The Author(s) 2018 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
Nath, Binita
Raza, Asif
Sethi, Vishal
Dalal, Amaresh
Ghosh, Siddhartha Sankar
Biswas, Gautam
Understanding flow dynamics, viability and metastatic potency of cervical cancer (HeLa) cells through constricted microchannel
title Understanding flow dynamics, viability and metastatic potency of cervical cancer (HeLa) cells through constricted microchannel
title_full Understanding flow dynamics, viability and metastatic potency of cervical cancer (HeLa) cells through constricted microchannel
title_fullStr Understanding flow dynamics, viability and metastatic potency of cervical cancer (HeLa) cells through constricted microchannel
title_full_unstemmed Understanding flow dynamics, viability and metastatic potency of cervical cancer (HeLa) cells through constricted microchannel
title_short Understanding flow dynamics, viability and metastatic potency of cervical cancer (HeLa) cells through constricted microchannel
title_sort understanding flow dynamics, viability and metastatic potency of cervical cancer (hela) cells through constricted microchannel
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6255798/
https://www.ncbi.nlm.nih.gov/pubmed/30478455
http://dx.doi.org/10.1038/s41598-018-35646-3
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