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<mods:namePart>Vay, Laura</mods:namePart>
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<mods:namePart>Hernández San Miguel, Esther</mods:namePart>
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<mods:namePart>Domínguez Lobatón, María Carmen</mods:namePart>
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<mods:namePart>Moreno Díaz-Calderón, Alfredo</mods:namePart>
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<mods:namePart>Montero Zoccola, María Teresa</mods:namePart>
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<mods:name>
<mods:role>
<mods:roleTerm type="text">author</mods:roleTerm>
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<mods:namePart>Álvarez Martín, Javier</mods:namePart>
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<mods:dateIssued encoding="iso8601">2009</mods:dateIssued>
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<mods:identifier type="citation">Cell Calcium, 2009, vol. 45, p. 243-250</mods:identifier>
<mods:identifier type="issn">0143-4160</mods:identifier>
<mods:identifier type="uri">http://uvadoc.uva.es/handle/10324/5985</mods:identifier>
<mods:identifier type="doi">10.1016/j.ceca.2008.10.007</mods:identifier>
<mods:identifier type="publicationfirstpage">243</mods:identifier>
<mods:identifier type="publicationlastpage">250</mods:identifier>
<mods:identifier type="publicationtitle">Cell Calcium</mods:identifier>
<mods:identifier type="publicationvolume">45</mods:identifier>
<mods:abstract>Mitochondrial Ca2+ activates many processes, from mitochondrial metabolism to opening of the permeability&#xd;
transition pore (PTP) and apoptosis. However, there is considerable controversy regarding the&#xd;
free mitochondrial [Ca2+] ([Ca2+]M) levels that can be attained during cell activation or even in mitochondrial&#xd;
preparations. Studies using fluorescent dyes (rhod-2 or similar), have reported that phosphate&#xd;
precipitation precludes [Ca2+]M from increasing above 2–3 M. Instead, using low-Ca2+-affinity aequorin&#xd;
probes, we have measured [Ca2+]M values more than two orders of magnitude higher. We confirm here&#xd;
these values by making a direct in situ calibration of mitochondrial aequorin, and we show that a prolonged&#xd;
increase in [Ca2+]M to levels of 0.5–1mM was actually observed at any phosphate concentration&#xd;
(0–10mM) during continuous perfusion of 3.5–100 MCa2+-buffers. In spite of this high and maintained&#xd;
(>10 min) [Ca2+]M, mitochondria retained functionality and the [Ca2+]M drop induced by a protonophore&#xd;
was fully reversible. In addition, this high [Ca2+]M did not induce PTP opening unless additional activators&#xd;
(phenyl arsine oxide, PAO) were present. PAO induced a rapid, concentration-dependent and irreversible&#xd;
drop in [Ca2+]M. In conclusion [Ca2+]M levels of 0.5–1mM can be reached and maintained for prolonged&#xd;
periods (>10 min) in phosphate-containing medium, and massive opening of PTP requires additional pore&#xd;
activators.</mods:abstract>
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<mods:accessCondition type="useAndReproduction">Attribution-NonCommercial-NoDerivatives 4.0 International</mods:accessCondition>
<mods:subject>
<mods:topic>Calcio - Metabolismo</mods:topic>
</mods:subject>
<mods:titleInfo>
<mods:title>Mitochondrial free [Ca2+] levels and the permeability transition</mods:title>
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