Ionic Components of Electric Current at Rat Corneal Wounds
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , , , , |
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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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 |
_version_ |
1814268345445253120 |