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Calcium-independent disruption of microtubule dynamics by nanosecond pulsed electric fields in U87 human glioblastoma cells

High powered, nanosecond duration, pulsed electric fields (nsPEF) cause cell death by a mechanism that is not fully understood and have been proposed as a targeted cancer therapy. Numerous chemotherapeutics work by disrupting microtubules. As microtubules are affected by electrical fields, this stud...

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Autores principales: Carr, Lynn, Bardet, Sylvia M., Burke, Ryan C., Arnaud-Cormos, Delia, Leveque, Philippe, O’Connor, Rodney P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259788/
https://www.ncbi.nlm.nih.gov/pubmed/28117459
http://dx.doi.org/10.1038/srep41267
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author Carr, Lynn
Bardet, Sylvia M.
Burke, Ryan C.
Arnaud-Cormos, Delia
Leveque, Philippe
O’Connor, Rodney P.
author_facet Carr, Lynn
Bardet, Sylvia M.
Burke, Ryan C.
Arnaud-Cormos, Delia
Leveque, Philippe
O’Connor, Rodney P.
author_sort Carr, Lynn
collection PubMed
description High powered, nanosecond duration, pulsed electric fields (nsPEF) cause cell death by a mechanism that is not fully understood and have been proposed as a targeted cancer therapy. Numerous chemotherapeutics work by disrupting microtubules. As microtubules are affected by electrical fields, this study looks at the possibility of disrupting them electrically with nsPEF. Human glioblastoma cells (U87-MG) treated with 100, 10 ns, 44 kV/cm pulses at a frequency of 10 Hz showed a breakdown of their interphase microtubule network that was accompanied by a reduction in the number of growing microtubules. This effect is temporally linked to loss of mitochondrial membrane potential and independent of cellular swelling and calcium influx, two factors that disrupt microtubule growth dynamics. Super-resolution microscopy revealed microtubule buckling and breaking as a result of nsPEF application, suggesting that nsPEF may act directly on microtubules.
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spelling pubmed-52597882017-01-25 Calcium-independent disruption of microtubule dynamics by nanosecond pulsed electric fields in U87 human glioblastoma cells Carr, Lynn Bardet, Sylvia M. Burke, Ryan C. Arnaud-Cormos, Delia Leveque, Philippe O’Connor, Rodney P. Sci Rep Article High powered, nanosecond duration, pulsed electric fields (nsPEF) cause cell death by a mechanism that is not fully understood and have been proposed as a targeted cancer therapy. Numerous chemotherapeutics work by disrupting microtubules. As microtubules are affected by electrical fields, this study looks at the possibility of disrupting them electrically with nsPEF. Human glioblastoma cells (U87-MG) treated with 100, 10 ns, 44 kV/cm pulses at a frequency of 10 Hz showed a breakdown of their interphase microtubule network that was accompanied by a reduction in the number of growing microtubules. This effect is temporally linked to loss of mitochondrial membrane potential and independent of cellular swelling and calcium influx, two factors that disrupt microtubule growth dynamics. Super-resolution microscopy revealed microtubule buckling and breaking as a result of nsPEF application, suggesting that nsPEF may act directly on microtubules. Nature Publishing Group 2017-01-24 /pmc/articles/PMC5259788/ /pubmed/28117459 http://dx.doi.org/10.1038/srep41267 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Carr, Lynn
Bardet, Sylvia M.
Burke, Ryan C.
Arnaud-Cormos, Delia
Leveque, Philippe
O’Connor, Rodney P.
Calcium-independent disruption of microtubule dynamics by nanosecond pulsed electric fields in U87 human glioblastoma cells
title Calcium-independent disruption of microtubule dynamics by nanosecond pulsed electric fields in U87 human glioblastoma cells
title_full Calcium-independent disruption of microtubule dynamics by nanosecond pulsed electric fields in U87 human glioblastoma cells
title_fullStr Calcium-independent disruption of microtubule dynamics by nanosecond pulsed electric fields in U87 human glioblastoma cells
title_full_unstemmed Calcium-independent disruption of microtubule dynamics by nanosecond pulsed electric fields in U87 human glioblastoma cells
title_short Calcium-independent disruption of microtubule dynamics by nanosecond pulsed electric fields in U87 human glioblastoma cells
title_sort calcium-independent disruption of microtubule dynamics by nanosecond pulsed electric fields in u87 human glioblastoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5259788/
https://www.ncbi.nlm.nih.gov/pubmed/28117459
http://dx.doi.org/10.1038/srep41267
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