Cargando…

Application of ECIS to Assess FCCP-Induced Changes of MSC Micromotion and Wound Healing Migration

Electric cell-substrate impedance sensing (ECIS) is an emerging technique for sensitively monitoring morphological changes of adherent cells in tissue culture. In this study, human mesenchymal stem cells (hMSCs) were exposed to different concentrations of carbonyl cyanide 4-(trifluoromethoxy)phenylh...

Descripción completa

Detalles Bibliográficos
Autores principales: Chiu, Sheng-Po, Lee, Yu-Wei, Wu, Ling-Yi, Tung, Tse-Hua, Gomez, Sofia, Lo, Chun-Min, Wang, Jia-Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679573/
https://www.ncbi.nlm.nih.gov/pubmed/31330904
http://dx.doi.org/10.3390/s19143210
_version_ 1783441366638919680
author Chiu, Sheng-Po
Lee, Yu-Wei
Wu, Ling-Yi
Tung, Tse-Hua
Gomez, Sofia
Lo, Chun-Min
Wang, Jia-Yi
author_facet Chiu, Sheng-Po
Lee, Yu-Wei
Wu, Ling-Yi
Tung, Tse-Hua
Gomez, Sofia
Lo, Chun-Min
Wang, Jia-Yi
author_sort Chiu, Sheng-Po
collection PubMed
description Electric cell-substrate impedance sensing (ECIS) is an emerging technique for sensitively monitoring morphological changes of adherent cells in tissue culture. In this study, human mesenchymal stem cells (hMSCs) were exposed to different concentrations of carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP) for 20 h and their subsequent concentration-dependent responses in micromotion and wound healing migration were measured by ECIS. FCCP disrupts ATP synthesis and results in a decrease in cell migration rates. To detect the change of cell micromotion in response to FCCP challenge, time-series resistances of cell-covered electrodes were monitored and the values of variance were calculated to verify the difference. While Seahorse XF-24 extracellular flux analyzer can detect the effect of FCCP at 3 μM concentration, the variance calculation of the time-series resistances measured at 4 kHz can detect the effect of FCCP at concentrations as low as 1 μM. For wound healing migration, the recovery resistance curves were fitted by sigmoid curve and the hill slope showed a concentration-dependent decline from 0.3 μM to 3 μM, indicating a decrease in cell migration rate. Moreover, dose dependent incline of the inflection points from 0.3 μM to 3 μM FCCP implied the increase of the half time for wound recovery migration. Together, our results demonstrate that partial uncoupling of mitochondrial oxidative phosphorylation reduces micromotion and wound healing migration of hMSCs. The ECIS method used in this study offers a simple and sensitive approach to investigate stem cell migration and its regulation by mitochondrial dynamics.
format Online
Article
Text
id pubmed-6679573
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-66795732019-08-19 Application of ECIS to Assess FCCP-Induced Changes of MSC Micromotion and Wound Healing Migration Chiu, Sheng-Po Lee, Yu-Wei Wu, Ling-Yi Tung, Tse-Hua Gomez, Sofia Lo, Chun-Min Wang, Jia-Yi Sensors (Basel) Article Electric cell-substrate impedance sensing (ECIS) is an emerging technique for sensitively monitoring morphological changes of adherent cells in tissue culture. In this study, human mesenchymal stem cells (hMSCs) were exposed to different concentrations of carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP) for 20 h and their subsequent concentration-dependent responses in micromotion and wound healing migration were measured by ECIS. FCCP disrupts ATP synthesis and results in a decrease in cell migration rates. To detect the change of cell micromotion in response to FCCP challenge, time-series resistances of cell-covered electrodes were monitored and the values of variance were calculated to verify the difference. While Seahorse XF-24 extracellular flux analyzer can detect the effect of FCCP at 3 μM concentration, the variance calculation of the time-series resistances measured at 4 kHz can detect the effect of FCCP at concentrations as low as 1 μM. For wound healing migration, the recovery resistance curves were fitted by sigmoid curve and the hill slope showed a concentration-dependent decline from 0.3 μM to 3 μM, indicating a decrease in cell migration rate. Moreover, dose dependent incline of the inflection points from 0.3 μM to 3 μM FCCP implied the increase of the half time for wound recovery migration. Together, our results demonstrate that partial uncoupling of mitochondrial oxidative phosphorylation reduces micromotion and wound healing migration of hMSCs. The ECIS method used in this study offers a simple and sensitive approach to investigate stem cell migration and its regulation by mitochondrial dynamics. MDPI 2019-07-21 /pmc/articles/PMC6679573/ /pubmed/31330904 http://dx.doi.org/10.3390/s19143210 Text en © 2019 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
Chiu, Sheng-Po
Lee, Yu-Wei
Wu, Ling-Yi
Tung, Tse-Hua
Gomez, Sofia
Lo, Chun-Min
Wang, Jia-Yi
Application of ECIS to Assess FCCP-Induced Changes of MSC Micromotion and Wound Healing Migration
title Application of ECIS to Assess FCCP-Induced Changes of MSC Micromotion and Wound Healing Migration
title_full Application of ECIS to Assess FCCP-Induced Changes of MSC Micromotion and Wound Healing Migration
title_fullStr Application of ECIS to Assess FCCP-Induced Changes of MSC Micromotion and Wound Healing Migration
title_full_unstemmed Application of ECIS to Assess FCCP-Induced Changes of MSC Micromotion and Wound Healing Migration
title_short Application of ECIS to Assess FCCP-Induced Changes of MSC Micromotion and Wound Healing Migration
title_sort application of ecis to assess fccp-induced changes of msc micromotion and wound healing migration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6679573/
https://www.ncbi.nlm.nih.gov/pubmed/31330904
http://dx.doi.org/10.3390/s19143210
work_keys_str_mv AT chiushengpo applicationofecistoassessfccpinducedchangesofmscmicromotionandwoundhealingmigration
AT leeyuwei applicationofecistoassessfccpinducedchangesofmscmicromotionandwoundhealingmigration
AT wulingyi applicationofecistoassessfccpinducedchangesofmscmicromotionandwoundhealingmigration
AT tungtsehua applicationofecistoassessfccpinducedchangesofmscmicromotionandwoundhealingmigration
AT gomezsofia applicationofecistoassessfccpinducedchangesofmscmicromotionandwoundhealingmigration
AT lochunmin applicationofecistoassessfccpinducedchangesofmscmicromotionandwoundhealingmigration
AT wangjiayi applicationofecistoassessfccpinducedchangesofmscmicromotionandwoundhealingmigration