Cargando…

Quantifying cell behaviors in negative-pressure induced monolayer cell movement

BACKGROUND: Negative-pressure of 125 mmHg (NP) has been shown to accelerate wound healing. Effects of NP on human keratinocyte behaviors during wound healing process were highlighted in this study. METHODS: An NP incubator incorporating the electric cell–substrate impedance sensing (ECIS) technique...

Descripción completa

Detalles Bibliográficos
Autores principales: Chow, Shu-Er, Chen, Carl Pai-Chu, Hsu, Chih-Chin, Tsai, Wen-Chung, Wang, Jong-Shyan, Hsu, Ning-Chun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chang Gung University 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138425/
https://www.ncbi.nlm.nih.gov/pubmed/27105598
http://dx.doi.org/10.1016/j.bj.2015.08.005
_version_ 1783355345229316096
author Chow, Shu-Er
Chen, Carl Pai-Chu
Hsu, Chih-Chin
Tsai, Wen-Chung
Wang, Jong-Shyan
Hsu, Ning-Chun
author_facet Chow, Shu-Er
Chen, Carl Pai-Chu
Hsu, Chih-Chin
Tsai, Wen-Chung
Wang, Jong-Shyan
Hsu, Ning-Chun
author_sort Chow, Shu-Er
collection PubMed
description BACKGROUND: Negative-pressure of 125 mmHg (NP) has been shown to accelerate wound healing. Effects of NP on human keratinocyte behaviors during wound healing process were highlighted in this study. METHODS: An NP incubator incorporating the electric cell–substrate impedance sensing (ECIS) technique has been built to quantify monolayer keratinocytes movement in serum-free media at the ambient pressure (AP) and NP for 12 h. Monolayer cell motions were continuously recorded by ECIS in the frequency range of 22.5–64 kHz. Membrane capacitance (C(m)), cell–substratum resistance (α), and cell–cell junction resistance (R(b)) were evaluated in cells at the different pressures. RESULTS: A greater monolayer cell migration distance was found in cells at NP. Decreased cell–substratum adhesion reflected in the significantly low α (AP:NP = ∼5 Ω(0.5):∼3 Ω(0.5)⋅cm), decreased integrin expression, and increased cell–substratum distance were seen in cells at NP. A significantly increased C(m) (AP:NP = ∼4:∼8 μF/cm(2)) in association with increased membrane ruffling and microtubule filaments were observed early in the monolayer cell movement at NP. A progressive drop in the R(b) from 1.2 Ω·cm(2) to 0.8 Ω·cm(2) corresponding to the gradually decreased E-cadherin expressions were observed 6 h after wound closure after NP treatment. CONCLUSION: A quick membrane ruffling formation, an early cell–substratum separation, and an ensuing decrease in the cellular interaction occur in cells at NP. These specific monolayer cell behaviors at NP have been quantified and possibly accelerate wound healing.
format Online
Article
Text
id pubmed-6138425
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Chang Gung University
record_format MEDLINE/PubMed
spelling pubmed-61384252018-09-27 Quantifying cell behaviors in negative-pressure induced monolayer cell movement Chow, Shu-Er Chen, Carl Pai-Chu Hsu, Chih-Chin Tsai, Wen-Chung Wang, Jong-Shyan Hsu, Ning-Chun Biomed J Original Article BACKGROUND: Negative-pressure of 125 mmHg (NP) has been shown to accelerate wound healing. Effects of NP on human keratinocyte behaviors during wound healing process were highlighted in this study. METHODS: An NP incubator incorporating the electric cell–substrate impedance sensing (ECIS) technique has been built to quantify monolayer keratinocytes movement in serum-free media at the ambient pressure (AP) and NP for 12 h. Monolayer cell motions were continuously recorded by ECIS in the frequency range of 22.5–64 kHz. Membrane capacitance (C(m)), cell–substratum resistance (α), and cell–cell junction resistance (R(b)) were evaluated in cells at the different pressures. RESULTS: A greater monolayer cell migration distance was found in cells at NP. Decreased cell–substratum adhesion reflected in the significantly low α (AP:NP = ∼5 Ω(0.5):∼3 Ω(0.5)⋅cm), decreased integrin expression, and increased cell–substratum distance were seen in cells at NP. A significantly increased C(m) (AP:NP = ∼4:∼8 μF/cm(2)) in association with increased membrane ruffling and microtubule filaments were observed early in the monolayer cell movement at NP. A progressive drop in the R(b) from 1.2 Ω·cm(2) to 0.8 Ω·cm(2) corresponding to the gradually decreased E-cadherin expressions were observed 6 h after wound closure after NP treatment. CONCLUSION: A quick membrane ruffling formation, an early cell–substratum separation, and an ensuing decrease in the cellular interaction occur in cells at NP. These specific monolayer cell behaviors at NP have been quantified and possibly accelerate wound healing. Chang Gung University 2016-02 2016-03-28 /pmc/articles/PMC6138425/ /pubmed/27105598 http://dx.doi.org/10.1016/j.bj.2015.08.005 Text en © 2016 Chang Gung University. Publishing services by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Chow, Shu-Er
Chen, Carl Pai-Chu
Hsu, Chih-Chin
Tsai, Wen-Chung
Wang, Jong-Shyan
Hsu, Ning-Chun
Quantifying cell behaviors in negative-pressure induced monolayer cell movement
title Quantifying cell behaviors in negative-pressure induced monolayer cell movement
title_full Quantifying cell behaviors in negative-pressure induced monolayer cell movement
title_fullStr Quantifying cell behaviors in negative-pressure induced monolayer cell movement
title_full_unstemmed Quantifying cell behaviors in negative-pressure induced monolayer cell movement
title_short Quantifying cell behaviors in negative-pressure induced monolayer cell movement
title_sort quantifying cell behaviors in negative-pressure induced monolayer cell movement
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138425/
https://www.ncbi.nlm.nih.gov/pubmed/27105598
http://dx.doi.org/10.1016/j.bj.2015.08.005
work_keys_str_mv AT chowshuer quantifyingcellbehaviorsinnegativepressureinducedmonolayercellmovement
AT chencarlpaichu quantifyingcellbehaviorsinnegativepressureinducedmonolayercellmovement
AT hsuchihchin quantifyingcellbehaviorsinnegativepressureinducedmonolayercellmovement
AT tsaiwenchung quantifyingcellbehaviorsinnegativepressureinducedmonolayercellmovement
AT wangjongshyan quantifyingcellbehaviorsinnegativepressureinducedmonolayercellmovement
AT hsuningchun quantifyingcellbehaviorsinnegativepressureinducedmonolayercellmovement