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<dc:creator>García-Sancho Martín, Francisco Javier</dc:creator>
<dc:date>2014</dc:date>
<dc:description>Producción Científica</dc:description>
<dc:description>Cross-talk between organelles and plasma membrane Ca2+ channels is essential for&#xd;
modulation of the cytosolic Ca2+ ([Ca2+]C) signals, but such modulation may differ among&#xd;
cells. In chromaffin cells Ca2+ entry through voltage-operated channels induces calcium release&#xd;
from the endoplasmic reticulum (ER) that amplifies the signal. [Ca2+]C microdomains as high&#xd;
as 20–50 μM are sensed by subplasmalemmal mitochondria, which accumulate large amounts of&#xd;
Ca2+ through the mitochondrial Ca2+ uniporter (MCU). Mitochondria confine the high-Ca2+&#xd;
microdomains (HCMDs) to beneath the plasma membrane,where exocytosis of secretory vesicles&#xd;
happens. Cell core [Ca2+]C is much smaller (1–2 μM). By acting as a Ca2+ sink, mitochondria&#xd;
stabilise theHCMDin space and time. In non-excitableHEK293 cells, activation of store-operated&#xd;
Ca2+ entry, triggered by ERCa2+ emptying, also generated subplasmalemmal HCMDs, but, in this&#xd;
case, most of the Ca2+ was taken up by the ER rather than bymitochondria. The smaller size of the&#xd;
[Ca2+]C peak in this case (about 2 μM)may contribute to this outcome, as the sarco-endoplasmic&#xd;
reticulum Ca2+ ATPase has much higher Ca2+ affinity than MCU. It is also possible that the relative positioning of organelles, channels and effectors, as well as cytoskeleton and accessory&#xd;
proteins plays an important role.</dc:description>
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<dc:identifier>http://uvadoc.uva.es/handle/10324/6348</dc:identifier>
<dc:language>eng</dc:language>
<dc:publisher>The Physiological Society</dc:publisher>
<dc:subject>Calcio - Absorción</dc:subject>
<dc:title>The coupling of plasma membrane calcium entry to calcium uptake by endoplasmic reticulum and mitochondria</dc:title>
<dc:type>info:eu-repo/semantics/article</dc:type>
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