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Prolonged calcium influx after termination of light-induced calcium release in invertebrate photoreceptors
In microvillar photoreceptors, light stimulates the phospholipase C cascade and triggers an elevation of cytosolic Ca(2+) that is essential for the regulation of both visual excitation and sensory adaptation. In some organisms, influx through light-activated ion channels contributes to the Ca(2+) in...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2737223/ https://www.ncbi.nlm.nih.gov/pubmed/19720959 http://dx.doi.org/10.1085/jgp.200910214 |
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author | del Pilar Gomez, Maria Nasi, Enrico |
author_facet | del Pilar Gomez, Maria Nasi, Enrico |
author_sort | del Pilar Gomez, Maria |
collection | PubMed |
description | In microvillar photoreceptors, light stimulates the phospholipase C cascade and triggers an elevation of cytosolic Ca(2+) that is essential for the regulation of both visual excitation and sensory adaptation. In some organisms, influx through light-activated ion channels contributes to the Ca(2+) increase. In contrast, in other species, such as Lima, Ca(2+) is initially only released from an intracellular pool, as the light-sensitive conductance is negligibly permeable to calcium ions. As a consequence, coping with sustained stimulation poses a challenge, requiring an alternative pathway for further calcium mobilization. We observed that after bright or prolonged illumination, the receptor potential of Lima photoreceptors is followed by the gradual development of an after-depolarization that decays in 1–4 minutes. Under voltage clamp, a graded, slow inward current (I(slow)) can be reproducibly elicited by flashes that saturate the photocurrent, and can reach a peak amplitude in excess of 200 pA. I(slow) obtains after replacing extracellular Na(+) with Li(+), guanidinium, or N-methyl-d-glucamine, indicating that it does not reflect the activation of an electrogenic Na/Ca exchange mechanism. An increase in membrane conductance accompanies the slow current. I(slow) is impervious to anion replacements and can be measured with extracellular Ca(2+) as the sole permeant species; Ba can substitute for Ca(2+) but Mg(2+) cannot. A persistent Ca(2+) elevation parallels I(slow), when no further internal release takes place. Thus, this slow current could contribute to sustained Ca(2+) mobilization and the concomitant regulation of the phototransduction machinery. Although reminiscent of the classical store depletion–operated calcium influx described in other cells, I(slow) appears to diverge in some significant aspects, such as its large size and insensitivity to SKF96365 and lanthanum; therefore, it may reflect an alternative mechanism for prolonged increase of cytosolic calcium in photoreceptors. |
format | Text |
id | pubmed-2737223 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27372232010-03-01 Prolonged calcium influx after termination of light-induced calcium release in invertebrate photoreceptors del Pilar Gomez, Maria Nasi, Enrico J Gen Physiol Article In microvillar photoreceptors, light stimulates the phospholipase C cascade and triggers an elevation of cytosolic Ca(2+) that is essential for the regulation of both visual excitation and sensory adaptation. In some organisms, influx through light-activated ion channels contributes to the Ca(2+) increase. In contrast, in other species, such as Lima, Ca(2+) is initially only released from an intracellular pool, as the light-sensitive conductance is negligibly permeable to calcium ions. As a consequence, coping with sustained stimulation poses a challenge, requiring an alternative pathway for further calcium mobilization. We observed that after bright or prolonged illumination, the receptor potential of Lima photoreceptors is followed by the gradual development of an after-depolarization that decays in 1–4 minutes. Under voltage clamp, a graded, slow inward current (I(slow)) can be reproducibly elicited by flashes that saturate the photocurrent, and can reach a peak amplitude in excess of 200 pA. I(slow) obtains after replacing extracellular Na(+) with Li(+), guanidinium, or N-methyl-d-glucamine, indicating that it does not reflect the activation of an electrogenic Na/Ca exchange mechanism. An increase in membrane conductance accompanies the slow current. I(slow) is impervious to anion replacements and can be measured with extracellular Ca(2+) as the sole permeant species; Ba can substitute for Ca(2+) but Mg(2+) cannot. A persistent Ca(2+) elevation parallels I(slow), when no further internal release takes place. Thus, this slow current could contribute to sustained Ca(2+) mobilization and the concomitant regulation of the phototransduction machinery. Although reminiscent of the classical store depletion–operated calcium influx described in other cells, I(slow) appears to diverge in some significant aspects, such as its large size and insensitivity to SKF96365 and lanthanum; therefore, it may reflect an alternative mechanism for prolonged increase of cytosolic calcium in photoreceptors. The Rockefeller University Press 2009-09 /pmc/articles/PMC2737223/ /pubmed/19720959 http://dx.doi.org/10.1085/jgp.200910214 Text en © 2009 Gomez and Nasi 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.jgp.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/). |
spellingShingle | Article del Pilar Gomez, Maria Nasi, Enrico Prolonged calcium influx after termination of light-induced calcium release in invertebrate photoreceptors |
title | Prolonged calcium influx after termination of light-induced calcium release in invertebrate photoreceptors |
title_full | Prolonged calcium influx after termination of light-induced calcium release in invertebrate photoreceptors |
title_fullStr | Prolonged calcium influx after termination of light-induced calcium release in invertebrate photoreceptors |
title_full_unstemmed | Prolonged calcium influx after termination of light-induced calcium release in invertebrate photoreceptors |
title_short | Prolonged calcium influx after termination of light-induced calcium release in invertebrate photoreceptors |
title_sort | prolonged calcium influx after termination of light-induced calcium release in invertebrate photoreceptors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2737223/ https://www.ncbi.nlm.nih.gov/pubmed/19720959 http://dx.doi.org/10.1085/jgp.200910214 |
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