High-voltage-activated calcium channels in Mueller cells acutely isolated from tiger salamander retina
Mueller cells mediate retinal function by stabilizing the ionic environment and signal glial network activity via calcium waves. Using whole-cell patch clamp recording, we describe a high-voltage-activated, slowly inactivating Ca channel current in isolated salamander Mueller cells that has unusual...
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Veröffentlicht in: | Glia 2005-01, Vol.49 (2), p.259-274 |
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creator | Welch, Nicole C Wood, Stephanie Jollimore, Christine Stevens, Kelly Kelly, Melanie EM Barnes, Steven |
description | Mueller cells mediate retinal function by stabilizing the ionic environment and signal glial network activity via calcium waves. Using whole-cell patch clamp recording, we describe a high-voltage-activated, slowly inactivating Ca channel current in isolated salamander Mueller cells that has unusual pharmacological properties. The Ca channel current has an activation midpoint of [sim]-8 mV and an inactivation midpoint of [sim]-26 mV in 10 mM Ba super(2+). The time constant for inactivation is [sim]380 ms at potentials positive to zero. The current is blocked by Cd super(2+) with an EC sub(50) of |
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Using whole-cell patch clamp recording, we describe a high-voltage-activated, slowly inactivating Ca channel current in isolated salamander Mueller cells that has unusual pharmacological properties. The Ca channel current has an activation midpoint of [sim]-8 mV and an inactivation midpoint of [sim]-26 mV in 10 mM Ba super(2+). The time constant for inactivation is [sim]380 ms at potentials positive to zero. The current is blocked by Cd super(2+) with an EC sub(50) of <100 nM. nisoldipine (10 [mu]M) blocks [sim]50%, while nifedipine (1 [mu]M), diltiazem (20 [mu]M), and verapamil (50 [mu]M) each block one-third of the current. In contrast to its typical actions, BayK 8644 blocks the current by [sim] 25%. Blockers of other Ca channel subtypes were also tested: [omega]-agatoxin IVA (200 nM) blocked only 13% of the Ca channel current, while [omega]-conotoxin GVIA (1 [mu]M) blocked 84% of the current. Immnohistochemistry supported the presence of [alpha]1A, [alpha]1B, [alpha]1C, and [alpha]1D Ca channel subunits. Mapping of dihydropyridine-binding sites with DM-BODIPY revealed a distribution of channels over the entire membrane of the Mueller cell with a higher density at the apical region. Overall, these observations suggest either the presence of a mix of L- and N-type Ca channels or a single, unconventional HVA Ca channel subtype sharing L- and N-type Ca channel characteristics.</description><identifier>ISSN: 0894-1491</identifier><identifier>DOI: 10.1002/glia.20113</identifier><language>eng</language><subject>Ambystoma tigrinum ; Caudata</subject><ispartof>Glia, 2005-01, Vol.49 (2), p.259-274</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids></links><search><creatorcontrib>Welch, Nicole C</creatorcontrib><creatorcontrib>Wood, Stephanie</creatorcontrib><creatorcontrib>Jollimore, Christine</creatorcontrib><creatorcontrib>Stevens, Kelly</creatorcontrib><creatorcontrib>Kelly, Melanie EM</creatorcontrib><creatorcontrib>Barnes, Steven</creatorcontrib><title>High-voltage-activated calcium channels in Mueller cells acutely isolated from tiger salamander retina</title><title>Glia</title><description>Mueller cells mediate retinal function by stabilizing the ionic environment and signal glial network activity via calcium waves. Using whole-cell patch clamp recording, we describe a high-voltage-activated, slowly inactivating Ca channel current in isolated salamander Mueller cells that has unusual pharmacological properties. The Ca channel current has an activation midpoint of [sim]-8 mV and an inactivation midpoint of [sim]-26 mV in 10 mM Ba super(2+). The time constant for inactivation is [sim]380 ms at potentials positive to zero. The current is blocked by Cd super(2+) with an EC sub(50) of <100 nM. nisoldipine (10 [mu]M) blocks [sim]50%, while nifedipine (1 [mu]M), diltiazem (20 [mu]M), and verapamil (50 [mu]M) each block one-third of the current. In contrast to its typical actions, BayK 8644 blocks the current by [sim] 25%. Blockers of other Ca channel subtypes were also tested: [omega]-agatoxin IVA (200 nM) blocked only 13% of the Ca channel current, while [omega]-conotoxin GVIA (1 [mu]M) blocked 84% of the current. Immnohistochemistry supported the presence of [alpha]1A, [alpha]1B, [alpha]1C, and [alpha]1D Ca channel subunits. Mapping of dihydropyridine-binding sites with DM-BODIPY revealed a distribution of channels over the entire membrane of the Mueller cell with a higher density at the apical region. 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Using whole-cell patch clamp recording, we describe a high-voltage-activated, slowly inactivating Ca channel current in isolated salamander Mueller cells that has unusual pharmacological properties. The Ca channel current has an activation midpoint of [sim]-8 mV and an inactivation midpoint of [sim]-26 mV in 10 mM Ba super(2+). The time constant for inactivation is [sim]380 ms at potentials positive to zero. The current is blocked by Cd super(2+) with an EC sub(50) of <100 nM. nisoldipine (10 [mu]M) blocks [sim]50%, while nifedipine (1 [mu]M), diltiazem (20 [mu]M), and verapamil (50 [mu]M) each block one-third of the current. In contrast to its typical actions, BayK 8644 blocks the current by [sim] 25%. Blockers of other Ca channel subtypes were also tested: [omega]-agatoxin IVA (200 nM) blocked only 13% of the Ca channel current, while [omega]-conotoxin GVIA (1 [mu]M) blocked 84% of the current. Immnohistochemistry supported the presence of [alpha]1A, [alpha]1B, [alpha]1C, and [alpha]1D Ca channel subunits. Mapping of dihydropyridine-binding sites with DM-BODIPY revealed a distribution of channels over the entire membrane of the Mueller cell with a higher density at the apical region. Overall, these observations suggest either the presence of a mix of L- and N-type Ca channels or a single, unconventional HVA Ca channel subtype sharing L- and N-type Ca channel characteristics.</abstract><doi>10.1002/glia.20113</doi></addata></record> |
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subjects | Ambystoma tigrinum Caudata |
title | High-voltage-activated calcium channels in Mueller cells acutely isolated from tiger salamander retina |
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