Study on the Expansion Dynamics of MDCK Epithelium by Interstitial Flow Using a Traction Force-Measurable Microfluidic Chip

The movement of collective cells is affected through changes in physical interactions of cells in response to external mechanical stimuli, including fluid flow. Most tissues are affected by fluid flow at the interstitial level, but few studies have investigated the physical effects in collective cel...

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Main Authors: Mirim Kim, Hwanseok Jang, Yongdoo Park
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Materials
Subjects:
Online Access:https://www.mdpi.com/1996-1944/14/4/935
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spelling doaj-26ab044670d649a097a3f8f3b26d9abd2021-02-17T00:03:15ZengMDPI AGMaterials1996-19442021-02-011493593510.3390/ma14040935Study on the Expansion Dynamics of MDCK Epithelium by Interstitial Flow Using a Traction Force-Measurable Microfluidic ChipMirim Kim0Hwanseok Jang1Yongdoo Park2Department of Biomedical Sciences, College of Medicine, Korea University, Seoul 02841, KoreaDepartment of Biomedical Sciences, College of Medicine, Korea University, Seoul 02841, KoreaDepartment of Biomedical Sciences, College of Medicine, Korea University, Seoul 02841, KoreaThe movement of collective cells is affected through changes in physical interactions of cells in response to external mechanical stimuli, including fluid flow. Most tissues are affected by fluid flow at the interstitial level, but few studies have investigated the physical effects in collective cells affected by a low flow rate. In this study, collective cell migration of Madin–Darby canine kidney (MDCK) epithelial cells was investigated under static or interstitial flow (0, 0.1, and 1 μL/min) using a traction microfluidic device. The optimization of calculation of cellular traction forces was first achieved by changing interrogation window size from the fluorescent bead images. Migration analysis of cell collectives patterned with a 700 μm circular shape reveals that cells under the slow flow (0.1 and 1 μL/min) showed the inhibitory migration by decreasing cell island size and cellular speed compared to that of static condition. Analysis of cellular forces shows that level of traction forces was lower in the slow flow condition (~20 Pa) compared to that of static condition (~50 Pa). Interestingly, the standard deviation of traction force of cells was dramatically decreased as the flow rate increased from 0 to 1 μL/min, which indicates that flow affects the distribution of cellular traction forces among cell collectives. Cellular tension was increased by 50% in the cells under the fluid flow rate of 1 μL/min. Treatment of calcium blocker increased the migratory speed of cells under the flow condition, whereas there is little change of cellular forces. In conclusion, it has been shown that the interstitial flow inhibited the collective movement of epithelial cells by decreasing and re-distributing cellular forces. These findings provide insights into the study of the effect of interstitial flow on cellular behavior, such as development, regeneration, and morphogenesis.https://www.mdpi.com/1996-1944/14/4/935fluid flowcollective cell migrationMDCKtraction force microscopymonolayer stress microscopymicrofluidics
collection DOAJ
language English
format Article
sources DOAJ
author Mirim Kim
Hwanseok Jang
Yongdoo Park
spellingShingle Mirim Kim
Hwanseok Jang
Yongdoo Park
Study on the Expansion Dynamics of MDCK Epithelium by Interstitial Flow Using a Traction Force-Measurable Microfluidic Chip
Materials
fluid flow
collective cell migration
MDCK
traction force microscopy
monolayer stress microscopy
microfluidics
author_facet Mirim Kim
Hwanseok Jang
Yongdoo Park
author_sort Mirim Kim
title Study on the Expansion Dynamics of MDCK Epithelium by Interstitial Flow Using a Traction Force-Measurable Microfluidic Chip
title_short Study on the Expansion Dynamics of MDCK Epithelium by Interstitial Flow Using a Traction Force-Measurable Microfluidic Chip
title_full Study on the Expansion Dynamics of MDCK Epithelium by Interstitial Flow Using a Traction Force-Measurable Microfluidic Chip
title_fullStr Study on the Expansion Dynamics of MDCK Epithelium by Interstitial Flow Using a Traction Force-Measurable Microfluidic Chip
title_full_unstemmed Study on the Expansion Dynamics of MDCK Epithelium by Interstitial Flow Using a Traction Force-Measurable Microfluidic Chip
title_sort study on the expansion dynamics of mdck epithelium by interstitial flow using a traction force-measurable microfluidic chip
publisher MDPI AG
series Materials
issn 1996-1944
publishDate 2021-02-01
description The movement of collective cells is affected through changes in physical interactions of cells in response to external mechanical stimuli, including fluid flow. Most tissues are affected by fluid flow at the interstitial level, but few studies have investigated the physical effects in collective cells affected by a low flow rate. In this study, collective cell migration of Madin–Darby canine kidney (MDCK) epithelial cells was investigated under static or interstitial flow (0, 0.1, and 1 μL/min) using a traction microfluidic device. The optimization of calculation of cellular traction forces was first achieved by changing interrogation window size from the fluorescent bead images. Migration analysis of cell collectives patterned with a 700 μm circular shape reveals that cells under the slow flow (0.1 and 1 μL/min) showed the inhibitory migration by decreasing cell island size and cellular speed compared to that of static condition. Analysis of cellular forces shows that level of traction forces was lower in the slow flow condition (~20 Pa) compared to that of static condition (~50 Pa). Interestingly, the standard deviation of traction force of cells was dramatically decreased as the flow rate increased from 0 to 1 μL/min, which indicates that flow affects the distribution of cellular traction forces among cell collectives. Cellular tension was increased by 50% in the cells under the fluid flow rate of 1 μL/min. Treatment of calcium blocker increased the migratory speed of cells under the flow condition, whereas there is little change of cellular forces. In conclusion, it has been shown that the interstitial flow inhibited the collective movement of epithelial cells by decreasing and re-distributing cellular forces. These findings provide insights into the study of the effect of interstitial flow on cellular behavior, such as development, regeneration, and morphogenesis.
topic fluid flow
collective cell migration
MDCK
traction force microscopy
monolayer stress microscopy
microfluidics
url https://www.mdpi.com/1996-1944/14/4/935
work_keys_str_mv AT mirimkim studyontheexpansiondynamicsofmdckepitheliumbyinterstitialflowusingatractionforcemeasurablemicrofluidicchip
AT hwanseokjang studyontheexpansiondynamicsofmdckepitheliumbyinterstitialflowusingatractionforcemeasurablemicrofluidicchip
AT yongdoopark studyontheexpansiondynamicsofmdckepitheliumbyinterstitialflowusingatractionforcemeasurablemicrofluidicchip
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