<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-28T19:01:52Z</responseDate><request verb="GetRecord" identifier="oai:uvadoc.uva.es:10324/5973" metadataPrefix="etdms">https://uvadoc.uva.es/oai/request</request><GetRecord><record><header><identifier>oai:uvadoc.uva.es:10324/5973</identifier><datestamp>2024-12-16T12:05:43Z</datestamp><setSpec>com_10324_1133</setSpec><setSpec>com_10324_931</setSpec><setSpec>com_10324_894</setSpec><setSpec>col_10324_1209</setSpec></header><metadata><thesis xmlns="http://www.ndltd.org/standards/metadata/etdms/1.0/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.ndltd.org/standards/metadata/etdms/1.0/ http://www.ndltd.org/standards/metadata/etdms/1.0/etdms.xsd">
<title>Calcium dynamics in catecholamine-containing secretory vesicles</title>
<creator>Moreno Díaz-Calderón, Alfredo</creator>
<creator>Domínguez Lobatón, María Carmen</creator>
<creator>Santo Domingo Mayoral, Jaime</creator>
<creator>Vay, Laura</creator>
<creator>Hernández San Miguel, Esther</creator>
<creator>Rizzuto, Rosario</creator>
<creator>Montero Zoccola, María Teresa</creator>
<creator>Álvarez Martín, Javier</creator>
<subject>Calcio en el organismo</subject>
<description>Producción Científica</description>
<description>We have used an aequorin chimera targeted to the membrane of the secretory granules to monitor the free [Ca2+] inside them in neurosecretory&#xd;
PC12 cells. More than 95% of the probe was located in a compartment with an homogeneous [Ca2+] around 40  M. Cell stimulation with&#xd;
either ATP, caffeine or high-K+ depolarization increased cytosolic [Ca2+] and decreased secretory granule [Ca2+] ([Ca2+]SG). Inositol-(1,4,5)-&#xd;
trisphosphate, cyclic ADP ribose and nicotinic acid adenine dinucleotide phosphate were all ineffective to release Ca2+ from the granules.&#xd;
Changes in cytosolic [Na+] (0–140 mM) or [Ca2+] (0–10 M) did not modify either ([Ca2+]SG). Instead, [Ca2+]SG was highly sensitive to&#xd;
changes in the pH gradient between the cytosol and the granules. Both carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone (FCCP) and&#xd;
nigericin, as well as cytosolic acidification, reversibly decreased [Ca2+]SG, while cytosolic alcalinization reversibly increased [Ca2+]SG. These&#xd;
results are consistent with the operation of a H+/Ca2+ antiporter in the vesicular membrane. This antiporter could also mediate the effects&#xd;
of ATP, caffeine and high-K+ on [Ca2+]SG, because all of them induced a transient cytosolic acidification. The FCCP-induced decrease in&#xd;
[Ca2+]SG was reversible in 10–15 min even in the absence of cytosolic Ca2+ or ATP, suggesting that most of the calcium content of the vesicles&#xd;
is bound to a slowly exchanging Ca2+ buffer. This large store buffers [Ca2+]SG changes in the long-term but allows highly dynamic free [Ca2+]SG&#xd;
changes to occur in seconds or minutes.</description>
<date>2014-09-16</date>
<date>2014-09-16</date>
<date>2005</date>
<type>info:eu-repo/semantics/article</type>
<identifier>Cell Calcium, 2005, vol. 37, p. 555-564</identifier>
<identifier>0143-4160</identifier>
<identifier>http://uvadoc.uva.es/handle/10324/5973</identifier>
<identifier>10.1016/j.ceca.2005.02.002</identifier>
<identifier>555</identifier>
<identifier>564</identifier>
<identifier>Cell Calcium</identifier>
<identifier>37</identifier>
<language>eng</language>
<rights>info:eu-repo/semantics/openAccess</rights>
<rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</rights>
<rights>Attribution-NonCommercial-NoDerivatives 4.0 International</rights>
<publisher>Elsevier Ltd.</publisher>
</thesis></metadata></record></GetRecord></OAI-PMH>