1987
DOI: 10.1016/0014-4827(87)90161-3
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Pathways of Ca2+ influx at the plasma membrane: Voltage-, receptor-, and second messenger-operated channels

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Cited by 221 publications
(53 citation statements)
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“…In a number, and possibly all cell types, the activation of receptors coupled to the hydrolysis of phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2] causes both release of Ca2 ' from intracellular stores and increased Ca2+ influx through the plasma membrane [33]. This latter event is generally thought to involve Ca2+ channels, mostly because the influx of Ca2+ depends on the transmembrane potential, i.e.…”
Section: Cu2+ Smocsmentioning
confidence: 99%
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“…In a number, and possibly all cell types, the activation of receptors coupled to the hydrolysis of phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2] causes both release of Ca2 ' from intracellular stores and increased Ca2+ influx through the plasma membrane [33]. This latter event is generally thought to involve Ca2+ channels, mostly because the influx of Ca2+ depends on the transmembrane potential, i.e.…”
Section: Cu2+ Smocsmentioning
confidence: 99%
“…(a) ROCs are those channels in which the ligand-binding site and the channel are either on the same polypeptide or in the same molecular complex [33]. Within the group of agonistactivated Ca" channels, Ca" ROCs are by far the best characterized in molecular and electrophysiological terms and incude the nicotinic channel, the N-methyl u-aspartate (MeDAsp) channel and perhaps, the ATP (external) gated channel( s).…”
Section: Receptor-activated and Second-messenger-activtrted Ca2+ Chanmentioning
confidence: 99%
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“…The mechanism by which muscarinic receptor occupancy allows Ca2t entry in these cells has been of considerable interest, with G-protein, second messenger, voltage and direct receptor-operated mechanisms being proposed (Meldolesi & Pozzan, 1987;Putney, 1990;Lambert & Nahorski, 1990b). …”
Section: Introductionmentioning
confidence: 99%
“…A similar inhibitory effect of TMB 8 on the zymosan-induced release of TxBz, PGE2 and PGD2 from cells prelabeled with [3H]arachidonic acid was observed (data not shown). Verapamil and nifedipine have been reported to inhibit Ca2+ influx from the extracellular space into excitable cells through Ca2 + channels located in the plasma membrane [22]. None of the calcium channel blockers (at a concentration of 100 pM) had a significant effect on the release of PGE2 by rat Kupffer cells after addition of zymosan, phorbol ester, A23187 or arachidonic acid (data not shown).…”
Section: Resultsmentioning
confidence: 88%