Ionic Components of Electric Current at Rat Corneal Wounds

Detalhes bibliográficos
Autor(a) principal: Vieira, Ana Carolina [UNIFESP]
Data de Publicação: 2011
Outros Autores: Reid, Brian, Cao, Lin, Mannis, Mark J., Schwab, Ivan R., Zhao, Min
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: http://dx.doi.org/10.1371/journal.pone.0017411
http://repositorio.unifesp.br/handle/11600/33475
Resumo: Background: Endogenous electric fields and currents occur naturally at wounds and are a strong signal guiding cell migration into the wound to promote healing. Many cells involved in wound healing respond to small physiological electric fields in vitro. It has long been assumed that wound electric fields are produced by passive ion leakage from damaged tissue. Could these fields be actively maintained and regulated as an active wound response? What are the molecular, ionic and cellular mechanisms underlying the wound electric currents?Methodology/Principal Findings: Using rat cornea wounds as a model, we measured the dynamic timecourses of individual ion fluxes with ion-selective probes. We also examined chloride channel expression before and after wounding. After wounding, Ca(2+) efflux increased steadily whereas K(+) showed an initial large efflux which rapidly decreased. Surprisingly, Na(+) flux at wounds was inward. A most significant observation was a persistent large influx of Cl(-), which had a time course similar to the net wound electric currents we have measured previously. Fixation of the tissues abolished ion fluxes. Pharmacological agents which stimulate ion transport significantly increased flux of Cl(-), Na(+) and K(+). Injury to the cornea caused significant changes in distribution and expression of Cl(-) channel CLC2.Conclusions/Significance: These data suggest that the outward electric currents occurring naturally at corneal wounds are carried mainly by a large influx of chloride ions, and in part by effluxes of calcium and potassium ions. Ca(2+) and Cl(-) fluxes appear to be mainly actively regulated, while K(+) flux appears to be largely due to leakage. the dynamic changes of electric currents and specific ion fluxes after wounding suggest that electrical signaling is an active response to injury and offers potential novel approaches to modulate wound healing, for example eye-drops targeting ion transport to aid in the challenging management of non-healing corneal ulcers.
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spelling Ionic Components of Electric Current at Rat Corneal WoundsBackground: Endogenous electric fields and currents occur naturally at wounds and are a strong signal guiding cell migration into the wound to promote healing. Many cells involved in wound healing respond to small physiological electric fields in vitro. It has long been assumed that wound electric fields are produced by passive ion leakage from damaged tissue. Could these fields be actively maintained and regulated as an active wound response? What are the molecular, ionic and cellular mechanisms underlying the wound electric currents?Methodology/Principal Findings: Using rat cornea wounds as a model, we measured the dynamic timecourses of individual ion fluxes with ion-selective probes. We also examined chloride channel expression before and after wounding. After wounding, Ca(2+) efflux increased steadily whereas K(+) showed an initial large efflux which rapidly decreased. Surprisingly, Na(+) flux at wounds was inward. A most significant observation was a persistent large influx of Cl(-), which had a time course similar to the net wound electric currents we have measured previously. Fixation of the tissues abolished ion fluxes. Pharmacological agents which stimulate ion transport significantly increased flux of Cl(-), Na(+) and K(+). Injury to the cornea caused significant changes in distribution and expression of Cl(-) channel CLC2.Conclusions/Significance: These data suggest that the outward electric currents occurring naturally at corneal wounds are carried mainly by a large influx of chloride ions, and in part by effluxes of calcium and potassium ions. Ca(2+) and Cl(-) fluxes appear to be mainly actively regulated, while K(+) flux appears to be largely due to leakage. the dynamic changes of electric currents and specific ion fluxes after wounding suggest that electrical signaling is an active response to injury and offers potential novel approaches to modulate wound healing, for example eye-drops targeting ion transport to aid in the challenging management of non-healing corneal ulcers.Univ Calif Davis, Dept Ophthalmol, Davis, CA 95616 USAUniversidade Federal de São Paulo, Dept Ophthalmol, São Paulo, BrazilUniv Calif Davis, Dept Dermatol, Davis, CA 95616 USAUniversidade Federal de São Paulo, Dept Ophthalmol, São Paulo, BrazilWeb of ScienceNational Institutes of Health National Eye InstituteWellcome TrustResearch to Prevent Blindness, Inc.NSFCUC Davis Dermatology DepartmentCalifornia Institute of Regenerative MedicineNSFNational Institutes of Health National Eye Institute: 1R01EY019101Wellcome Trust: 068012NSFC: 30628026California Institute of Regenerative Medicine: RB1-01417NSF: MCB-0951199Public Library ScienceUniv Calif DavisUniversidade Federal de São Paulo (UNIFESP)Vieira, Ana Carolina [UNIFESP]Reid, BrianCao, LinMannis, Mark J.Schwab, Ivan R.Zhao, Min2016-01-24T14:06:12Z2016-01-24T14:06:12Z2011-02-25info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion12application/pdfhttp://dx.doi.org/10.1371/journal.pone.0017411Plos One. San Francisco: Public Library Science, v. 6, n. 2, 12 p., 2011.10.1371/journal.pone.0017411WOS000287764100057.pdf1932-6203http://repositorio.unifesp.br/handle/11600/33475WOS:000287764100057engPlos Oneinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-31T14:54:40Zoai:repositorio.unifesp.br/:11600/33475Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-31T14:54:40Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Ionic Components of Electric Current at Rat Corneal Wounds
title Ionic Components of Electric Current at Rat Corneal Wounds
spellingShingle Ionic Components of Electric Current at Rat Corneal Wounds
Vieira, Ana Carolina [UNIFESP]
title_short Ionic Components of Electric Current at Rat Corneal Wounds
title_full Ionic Components of Electric Current at Rat Corneal Wounds
title_fullStr Ionic Components of Electric Current at Rat Corneal Wounds
title_full_unstemmed Ionic Components of Electric Current at Rat Corneal Wounds
title_sort Ionic Components of Electric Current at Rat Corneal Wounds
author Vieira, Ana Carolina [UNIFESP]
author_facet Vieira, Ana Carolina [UNIFESP]
Reid, Brian
Cao, Lin
Mannis, Mark J.
Schwab, Ivan R.
Zhao, Min
author_role author
author2 Reid, Brian
Cao, Lin
Mannis, Mark J.
Schwab, Ivan R.
Zhao, Min
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Univ Calif Davis
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Vieira, Ana Carolina [UNIFESP]
Reid, Brian
Cao, Lin
Mannis, Mark J.
Schwab, Ivan R.
Zhao, Min
description Background: Endogenous electric fields and currents occur naturally at wounds and are a strong signal guiding cell migration into the wound to promote healing. Many cells involved in wound healing respond to small physiological electric fields in vitro. It has long been assumed that wound electric fields are produced by passive ion leakage from damaged tissue. Could these fields be actively maintained and regulated as an active wound response? What are the molecular, ionic and cellular mechanisms underlying the wound electric currents?Methodology/Principal Findings: Using rat cornea wounds as a model, we measured the dynamic timecourses of individual ion fluxes with ion-selective probes. We also examined chloride channel expression before and after wounding. After wounding, Ca(2+) efflux increased steadily whereas K(+) showed an initial large efflux which rapidly decreased. Surprisingly, Na(+) flux at wounds was inward. A most significant observation was a persistent large influx of Cl(-), which had a time course similar to the net wound electric currents we have measured previously. Fixation of the tissues abolished ion fluxes. Pharmacological agents which stimulate ion transport significantly increased flux of Cl(-), Na(+) and K(+). Injury to the cornea caused significant changes in distribution and expression of Cl(-) channel CLC2.Conclusions/Significance: These data suggest that the outward electric currents occurring naturally at corneal wounds are carried mainly by a large influx of chloride ions, and in part by effluxes of calcium and potassium ions. Ca(2+) and Cl(-) fluxes appear to be mainly actively regulated, while K(+) flux appears to be largely due to leakage. the dynamic changes of electric currents and specific ion fluxes after wounding suggest that electrical signaling is an active response to injury and offers potential novel approaches to modulate wound healing, for example eye-drops targeting ion transport to aid in the challenging management of non-healing corneal ulcers.
publishDate 2011
dc.date.none.fl_str_mv 2011-02-25
2016-01-24T14:06:12Z
2016-01-24T14:06:12Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1371/journal.pone.0017411
Plos One. San Francisco: Public Library Science, v. 6, n. 2, 12 p., 2011.
10.1371/journal.pone.0017411
WOS000287764100057.pdf
1932-6203
http://repositorio.unifesp.br/handle/11600/33475
WOS:000287764100057
url http://dx.doi.org/10.1371/journal.pone.0017411
http://repositorio.unifesp.br/handle/11600/33475
identifier_str_mv Plos One. San Francisco: Public Library Science, v. 6, n. 2, 12 p., 2011.
10.1371/journal.pone.0017411
WOS000287764100057.pdf
1932-6203
WOS:000287764100057
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Plos One
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 12
application/pdf
dc.publisher.none.fl_str_mv Public Library Science
publisher.none.fl_str_mv Public Library Science
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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