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pubmed-article:9838027pubmed:abstractTextThe three subtypes of inositol trisphosphate (InsP3) receptor expressed in mammalian cells are each capable of forming intracellular Ca2+ channels that are regulated by both InsP3 and cytosolic Ca2+. The InsP3 receptors of many, though perhaps not all, tissues are biphasically regulated by cytosolic Ca2+: a rapid stimulation of the receptors by modest increases in Ca2+ concentration is followed by a slower inhibition at higher Ca2+ concentrations. Despite the widespread occurrence of this form of regulation and the belief that it is an important element of the mechanisms responsible for the complex Ca2+ signals evoked by physiological stimuli, the underlying mechanisms are not understood. Both accessory proteins and Ca2+-binding sites on InsP3 receptors themselves have been proposed to mediate the effects of cytosolic Ca2+ on InsP3 receptor function, but the evidence is equivocal. The effects of cytosolic Ca2+ on InsP3 binding and channel opening, and the possible means whereby the effects are mediated are discussed in this review.lld:pubmed
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pubmed-article:9838027pubmed:articleTitleInositol trisphosphate receptors: Ca2+-modulated intracellular Ca2+ channels.lld:pubmed
pubmed-article:9838027pubmed:affiliationDepartment of Pharmacology, Tennis Court Road, Cambridge CB2 1QJ, UK. cwt1000@cam.ac.uklld:pubmed
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