A low affinity Ca2+ receptor controls the final steps in peptide secretion from pituitary melanotrophs

Using flash photolysis of caged Ca2+ and the membrane capacitance to monitor exocytosis, we have studied the response of single melanotrophs to a step rise in cytosolic Ca2+ concentration ([Ca2+]i). Exocytosis begins with a rapid burst. This burst is followed by a slower phase, which is inhibited at...

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Published inNeuron (Cambridge, Mass.) Vol. 11; no. 1; pp. 93 - 104
Main Authors THOMAS, P, WONG, J. G, LEE, A. K, ALMERS, W
Format Journal Article
LanguageEnglish
Published Cambridge, MA Cell Press 01.07.1993
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Summary:Using flash photolysis of caged Ca2+ and the membrane capacitance to monitor exocytosis, we have studied the response of single melanotrophs to a step rise in cytosolic Ca2+ concentration ([Ca2+]i). Exocytosis begins with a rapid burst. This burst is followed by a slower phase, which is inhibited at cytosolic pH 6.2, and an ultraslow phase, which is strongly temperature sensitive. The exocytic burst starts with a delay of 6-11 ms and continues at a rate that grows steeply with [Ca2+]i and is half-maximal at [Ca2+]i = 27 microM. At least 3 Ca2+ ions are required to trigger exocytosis. The rate constant at saturating [Ca2+]i suggests that exocytosis of a dense core vesicle takes 40 ms after all Ca2+ ions have bound to their regulatory sites. If docked dense core vesicles cause the exocytic burst, they must decorate the plasma membrane at a mean density of 0.5/micron2.
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ISSN:0896-6273
1097-4199
DOI:10.1016/0896-6273(93)90274-U