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Developmental regulation of calcium-dependent feedback in Xenopus rods

The kinetics of activation and inactivation in the phototransduction pathway of developing Xenopus rods were studied. The gain of the activation steps in transduction (amplification) increased and photoresponses became more rapid as the rods matured from the larval to the adult stage. The time to pe...

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Autores principales: Solessio, Eduardo, Mani, Shobana S., Cuenca, Nicolas, Engbretson, Gustav A., Barlow, Robert B., Knox, Barry E.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2234010/
https://www.ncbi.nlm.nih.gov/pubmed/15504902
http://dx.doi.org/10.1085/jgp.200409162
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author Solessio, Eduardo
Mani, Shobana S.
Cuenca, Nicolas
Engbretson, Gustav A.
Barlow, Robert B.
Knox, Barry E.
author_facet Solessio, Eduardo
Mani, Shobana S.
Cuenca, Nicolas
Engbretson, Gustav A.
Barlow, Robert B.
Knox, Barry E.
author_sort Solessio, Eduardo
collection PubMed
description The kinetics of activation and inactivation in the phototransduction pathway of developing Xenopus rods were studied. The gain of the activation steps in transduction (amplification) increased and photoresponses became more rapid as the rods matured from the larval to the adult stage. The time to peak was significantly shorter in adults (1.3 s) than tadpoles (2 s). Moreover, adult rods recovered twice as fast from saturating flashes than did larval rods without changes of the dominant time constant (2.5 s). Guanylate cyclase (GC) activity, determined using IBMX steps, increased in adult rods from ∼1.1 s(−1) to 3.7 s(−1) 5 s after a saturating flash delivering 6,000 photoisomerizations. In larval rods, it increased from 1.8 s(−1) to 4.0 s(−1) 9 s after an equivalent flash. However, the ratio of amplification to the measured dark phosphodiesterase activity was constant. Guanylate cyclase–activating protein (GCAP1) levels and normalized Na(+)/Ca(2+), K(+) exchanger currents were increased in adults compared with tadpoles. Together, these results are consistent with the acceleration of the recovery phase in adult rods via developmental regulation of calcium homeostasis. Despite these large changes, the single photon response amplitude was ∼0.6 pA throughout development. Reduction of calcium feedback with BAPTA increased adult single photon response amplitudes threefold and reduced its cutoff frequency to that observed with tadpole rods. Linear mathematical modeling suggests that calcium-dependent feedback can account for the observed differences in the power spectra of larval and adult rods. We conclude that larval Xenopus maximize sensitivity at the expense of slower response kinetics while adults maximize response kinetics at the expense of sensitivity.
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spelling pubmed-22340102008-03-21 Developmental regulation of calcium-dependent feedback in Xenopus rods Solessio, Eduardo Mani, Shobana S. Cuenca, Nicolas Engbretson, Gustav A. Barlow, Robert B. Knox, Barry E. J Gen Physiol Article The kinetics of activation and inactivation in the phototransduction pathway of developing Xenopus rods were studied. The gain of the activation steps in transduction (amplification) increased and photoresponses became more rapid as the rods matured from the larval to the adult stage. The time to peak was significantly shorter in adults (1.3 s) than tadpoles (2 s). Moreover, adult rods recovered twice as fast from saturating flashes than did larval rods without changes of the dominant time constant (2.5 s). Guanylate cyclase (GC) activity, determined using IBMX steps, increased in adult rods from ∼1.1 s(−1) to 3.7 s(−1) 5 s after a saturating flash delivering 6,000 photoisomerizations. In larval rods, it increased from 1.8 s(−1) to 4.0 s(−1) 9 s after an equivalent flash. However, the ratio of amplification to the measured dark phosphodiesterase activity was constant. Guanylate cyclase–activating protein (GCAP1) levels and normalized Na(+)/Ca(2+), K(+) exchanger currents were increased in adults compared with tadpoles. Together, these results are consistent with the acceleration of the recovery phase in adult rods via developmental regulation of calcium homeostasis. Despite these large changes, the single photon response amplitude was ∼0.6 pA throughout development. Reduction of calcium feedback with BAPTA increased adult single photon response amplitudes threefold and reduced its cutoff frequency to that observed with tadpole rods. Linear mathematical modeling suggests that calcium-dependent feedback can account for the observed differences in the power spectra of larval and adult rods. We conclude that larval Xenopus maximize sensitivity at the expense of slower response kinetics while adults maximize response kinetics at the expense of sensitivity. The Rockefeller University Press 2004-11 /pmc/articles/PMC2234010/ /pubmed/15504902 http://dx.doi.org/10.1085/jgp.200409162 Text en Copyright © 2004, The Rockefeller University Press 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 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Solessio, Eduardo
Mani, Shobana S.
Cuenca, Nicolas
Engbretson, Gustav A.
Barlow, Robert B.
Knox, Barry E.
Developmental regulation of calcium-dependent feedback in Xenopus rods
title Developmental regulation of calcium-dependent feedback in Xenopus rods
title_full Developmental regulation of calcium-dependent feedback in Xenopus rods
title_fullStr Developmental regulation of calcium-dependent feedback in Xenopus rods
title_full_unstemmed Developmental regulation of calcium-dependent feedback in Xenopus rods
title_short Developmental regulation of calcium-dependent feedback in Xenopus rods
title_sort developmental regulation of calcium-dependent feedback in xenopus rods
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2234010/
https://www.ncbi.nlm.nih.gov/pubmed/15504902
http://dx.doi.org/10.1085/jgp.200409162
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