Cargando…

Voltage-clamp recordings of light responses from wild-type and mutant mouse cone photoreceptors

We describe the first extensive study of voltage-clamp current responses of cone photoreceptors in unlabeled, dark-adapted mouse retina using only the position and appearance of cone somata as a guide. Identification was confirmed from morphology after dye filling. Photocurrents recorded from wild-t...

Descripción completa

Detalles Bibliográficos
Autores principales: Ingram, Norianne T., Sampath, Alapakkam P., Fain, Gordon L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829558/
https://www.ncbi.nlm.nih.gov/pubmed/31562185
http://dx.doi.org/10.1085/jgp.201912419
_version_ 1783465584897294336
author Ingram, Norianne T.
Sampath, Alapakkam P.
Fain, Gordon L.
author_facet Ingram, Norianne T.
Sampath, Alapakkam P.
Fain, Gordon L.
author_sort Ingram, Norianne T.
collection PubMed
description We describe the first extensive study of voltage-clamp current responses of cone photoreceptors in unlabeled, dark-adapted mouse retina using only the position and appearance of cone somata as a guide. Identification was confirmed from morphology after dye filling. Photocurrents recorded from wild-type mouse cones were biphasic with a fast cone component and a slower rod component. The rod component could be eliminated with dim background light and was not present in mouse lines lacking the rod transducin-α subunit (Gnat1(−/−)) or connexin 36 (Cx36(−/−)). Cones from Gnat1(−/−) or Cx36(−/−) mice had resting membrane potentials between −45 and −55 mV, peak photocurrents of 20–25 picoamps (pA) at a membrane potential V(m) = −50 mV, sensitivities 60–70 times smaller than rods, and a total membrane capacitance two to four times greater than rods. The rate of activation (amplification constant) was largely independent of the brightness of the flash and was 1–2 s(−2), less than half that of rods. The role of Ca(2+)-dependent transduction modulation was investigated by recording from cones in mice lacking rod transducin (Gnat1), recoverin, and/or the guanylyl-cyclase–activating proteins (GCAPs). In confirmation of previous results, responses of Gnat1(−/−);Gcaps(−/−) cones and triple-mutant Gnat1(−/−);Gcaps(−/−);Rv(−/−) cones recovered more slowly both to light flashes and steps and were more sensitive than cones expressing the GCAPs. Cones from all four mouse lines showed significant recovery and escaped saturation even in bright background light. This recovery occurred too rapidly to be caused by pigment bleaching or metaII decay and appears to reflect some modulation of response inactivation in addition to those produced by recoverin and the GCAPs. Our experiments now make possible a more detailed understanding of the cellular physiology of mammalian cone photoreceptors and the role of conductances in the inner and outer segment in producing cone light responses.
format Online
Article
Text
id pubmed-6829558
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Rockefeller University Press
record_format MEDLINE/PubMed
spelling pubmed-68295582020-05-04 Voltage-clamp recordings of light responses from wild-type and mutant mouse cone photoreceptors Ingram, Norianne T. Sampath, Alapakkam P. Fain, Gordon L. J Gen Physiol Research Articles We describe the first extensive study of voltage-clamp current responses of cone photoreceptors in unlabeled, dark-adapted mouse retina using only the position and appearance of cone somata as a guide. Identification was confirmed from morphology after dye filling. Photocurrents recorded from wild-type mouse cones were biphasic with a fast cone component and a slower rod component. The rod component could be eliminated with dim background light and was not present in mouse lines lacking the rod transducin-α subunit (Gnat1(−/−)) or connexin 36 (Cx36(−/−)). Cones from Gnat1(−/−) or Cx36(−/−) mice had resting membrane potentials between −45 and −55 mV, peak photocurrents of 20–25 picoamps (pA) at a membrane potential V(m) = −50 mV, sensitivities 60–70 times smaller than rods, and a total membrane capacitance two to four times greater than rods. The rate of activation (amplification constant) was largely independent of the brightness of the flash and was 1–2 s(−2), less than half that of rods. The role of Ca(2+)-dependent transduction modulation was investigated by recording from cones in mice lacking rod transducin (Gnat1), recoverin, and/or the guanylyl-cyclase–activating proteins (GCAPs). In confirmation of previous results, responses of Gnat1(−/−);Gcaps(−/−) cones and triple-mutant Gnat1(−/−);Gcaps(−/−);Rv(−/−) cones recovered more slowly both to light flashes and steps and were more sensitive than cones expressing the GCAPs. Cones from all four mouse lines showed significant recovery and escaped saturation even in bright background light. This recovery occurred too rapidly to be caused by pigment bleaching or metaII decay and appears to reflect some modulation of response inactivation in addition to those produced by recoverin and the GCAPs. Our experiments now make possible a more detailed understanding of the cellular physiology of mammalian cone photoreceptors and the role of conductances in the inner and outer segment in producing cone light responses. Rockefeller University Press 2019-11-04 2019-09-27 /pmc/articles/PMC6829558/ /pubmed/31562185 http://dx.doi.org/10.1085/jgp.201912419 Text en © 2019 Fain et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Research Articles
Ingram, Norianne T.
Sampath, Alapakkam P.
Fain, Gordon L.
Voltage-clamp recordings of light responses from wild-type and mutant mouse cone photoreceptors
title Voltage-clamp recordings of light responses from wild-type and mutant mouse cone photoreceptors
title_full Voltage-clamp recordings of light responses from wild-type and mutant mouse cone photoreceptors
title_fullStr Voltage-clamp recordings of light responses from wild-type and mutant mouse cone photoreceptors
title_full_unstemmed Voltage-clamp recordings of light responses from wild-type and mutant mouse cone photoreceptors
title_short Voltage-clamp recordings of light responses from wild-type and mutant mouse cone photoreceptors
title_sort voltage-clamp recordings of light responses from wild-type and mutant mouse cone photoreceptors
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6829558/
https://www.ncbi.nlm.nih.gov/pubmed/31562185
http://dx.doi.org/10.1085/jgp.201912419
work_keys_str_mv AT ingramnoriannet voltageclamprecordingsoflightresponsesfromwildtypeandmutantmouseconephotoreceptors
AT sampathalapakkamp voltageclamprecordingsoflightresponsesfromwildtypeandmutantmouseconephotoreceptors
AT faingordonl voltageclamprecordingsoflightresponsesfromwildtypeandmutantmouseconephotoreceptors