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dc.contributor.author
Fernández, Juan Manuel Francisco  
dc.contributor.author
Di Giusto, Gisela  
dc.contributor.author
Kalstein, Maia  
dc.contributor.author
Melamud, Luciana  
dc.contributor.author
Rivarola, Valeria  
dc.contributor.author
Ford, Paula  
dc.contributor.author
Capurro, Claudia Graciela  
dc.date.available
2015-08-19T14:01:33Z  
dc.date.issued
2013-02-25  
dc.identifier.citation
Fernández, Juan Manuel Francisco; Di Giusto, Gisela; Kalstein, Maia; Melamud, Luciana; Rivarola, Valeria; et al.; Cell Volume Regulation in Human Retinal Müller Cells is Associated with Changes in Transmembrane Potential; Public Library of Science; Plos One; 8; 2; 25-2-2013; 1-11  
dc.identifier.issn
1932-6203  
dc.identifier.uri
http://hdl.handle.net/11336/1724  
dc.description.abstract
Müller cells are mainly involved in controlling extracellular homeostasis in the retina, where intense neural activity alters ion concentrations and osmotic gradients, thus favoring cell swelling. This increase in cell volume is followed by a regulatory volume decrease response (RVD), which is known to be partially mediated by the activation of K and anion channels. However, the precise mechanisms underlying osmotic swelling and subsequent cell volume regulation in Müller cells have been evaluated by only a few studies. Although the activation of ion channels during the RVD response may alter transmembrane potential (V), no studies have actually addressed this issue in Müller cells. The aim of the present work is to evaluate RVD using a retinal Müller cell line (MIO-M1) under different extracellular ionic conditions, and to study a possible association between RVD and changes in V. Cell volume and V changes were evaluated using fluorescent probe techniques and a mathematical model. Results show that cell swelling and subsequent RVD were accompanied by V depolarization followed by repolarization. This response depended on the composition of extracellular media. Cells exposed to a hypoosmotic solution with reduced ionic strength underwent maximum RVD and had a larger repolarization. Both of these responses were reduced by K or Cl channel blockers. In contrast, cells facing a hypoosmotic solution with the same ionic strength as the isoosmotic solution showed a lower RVD and a smaller repolarization and were not affected by blockers. Together, experimental and simulated data led us to propose that the efficiency of the RVD process in Müller glia depends not only on the activation of ion channels, but is also strongly modulated by concurrent changes in the membrane potential. The relationship between ionic fluxes, changes in ion permeabilities and ion concentrations -all leading to changes in V- define the success of RVD.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Public Library of Science  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Aqp  
dc.subject
Muller Cells  
dc.subject
Simulation  
dc.subject
Volume Regulation  
dc.subject.classification
Bioquímica y Biología Molecular  
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Medicina Básica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
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Oftalmología  
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Medicina Clínica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Cell Volume Regulation in Human Retinal Müller Cells is Associated with Changes in Transmembrane Potential  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2016-03-30 10:35:44.97925-03  
dc.journal.volume
8  
dc.journal.number
2  
dc.journal.pagination
1-11  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
San Francisco  
dc.description.fil
Fil: Fernández, Juan Manuel Francisco. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas; Argentina; Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas. Laboratorio de Biomembranas; Argentina;  
dc.description.fil
Fil: Di Giusto, Gisela. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas. Laboratorio de Biomembranas; Argentina;  
dc.description.fil
Fil: Kalstein, Maia. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas. Laboratorio de Biomembranas; Argentina;  
dc.description.fil
Fil: Melamud, Luciana. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas. Laboratorio de Biomembranas; Argentina; Universidad de Buenos Aires. Facultad de Medicina. Centro Universitario de Neurología Dr. J.M. Ramos Mejía. Consultorio de Neuroinmunología; Argentina;  
dc.description.fil
Fil: Rivarola, Valeria. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas; Argentina; Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas. Laboratorio de Biomembranas; Argentina;  
dc.description.fil
Fil: Ford, Paula. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas; Argentina; Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas. Laboratorio de Biomembranas; Argentina;  
dc.description.fil
Fil: Capurro, Claudia Graciela. Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas; Argentina; Universidad de Buenos Aires. Facultad de Medicina. Departamento de Ciencias Fisiológicas. Laboratorio de Biomembranas; Argentina;  
dc.journal.title
Plos One  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581454/pdf/pone.0057268.pdf  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://europepmc.org/backend/ptpmcrender.fcgi?accid=PMC3581454&blobtype=pdf  
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info:eu-repo/semantics/altIdentifier/url/http://www.biomedsearch.com/nih/Cell-volume-regulation-in-cultured/23451196.html  
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info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/doi:10.1371/journal.pone.0057268  
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info:eu-repo/semantics/altIdentifier/url/http://www.plosone.org/article/fetchObject.action?uri=info:doi/10.1371/journal.pone.0057268&representation=PDF