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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dirros.openscience.si/IzpisGradiva.php?id=20828"><dc:title>Mitochondria can substitute for parvalbumin to lowercytosolic calcium levels in the murine fast skeletal muscle</dc:title><dc:creator>Marcucci,	Lorenzo	(Avtor)
	</dc:creator><dc:creator>Nogara,	Leonardo	(Avtor)
	</dc:creator><dc:creator>Canato,	Marta	(Avtor)
	</dc:creator><dc:creator>Germinario,	Elena	(Avtor)
	</dc:creator><dc:creator>Raffaello,	Anna	(Avtor)
	</dc:creator><dc:creator>Carraro,	Michela	(Avtor)
	</dc:creator><dc:creator>Bernardi,	Paolo	(Avtor)
	</dc:creator><dc:creator>Pietrangelo,	Laura	(Avtor)
	</dc:creator><dc:creator>Boncompagni,	Simona	(Avtor)
	</dc:creator><dc:creator>Protasi,	Feliciano	(Avtor)
	</dc:creator><dc:creator>Paolocci,	Nazareno	(Avtor)
	</dc:creator><dc:creator>Reggiani,	Carlo	(Avtor)
	</dc:creator><dc:subject>calcium</dc:subject><dc:subject>mitochondria</dc:subject><dc:subject>mouse skeletal muscle fibers</dc:subject><dc:subject>parvalbumin</dc:subject><dc:subject>reaction-diffusion model</dc:subject><dc:description>Aim: Parvalbumin (PV) is a primary calcium buffer in mouse fast skeletal musclefibers. Previous work showed that PV ablation has a limited impact on cytosolicCa2+ ([Ca2+]cyto) transients and contractile response, while it enhances mitochon-drial density and mitochondrial matrix-free calcium concentration ([Ca2+]mito).Here, we aimed to quantitatively test the hypothesis that mitochondria act tocompensate for PV deficiency.Methods: We determined the free Ca 2+ redistribution during a 2 s 60 Hz tetanicstimulation in the sarcoplasmic reticulum, cytosol, and mitochondria. Via a re-action–diffusion Ca 2+ model, we quantitatively evaluated mitochondrial uptakeand storage capacity requirements to compensate for PV lack and analyzed pos-sible extracellular export.Results: [Ca 2+]mito during tetanic stimulation is greater in knock-out (KO)(1362 ± 392 nM) than in wild-type (WT) (855 ± 392 nM), p &lt; 0.05. Under the as-sumption of a non-linear intramitochondrial buffering, the model predicts an ac-cumulation of 725 μmoles/Lfiber (buffering ratio 1:11 000) in KO, much higherthan in WT (137 μmoles/Lfiber, ratio 1:4500). The required transport rate via mi-tochondrial calcium uniporter (MCU) reaches 3 mM/s, compatible with availableliterature. TEM images of calcium entry units and Mn2+ quenching showed a greater capacity of store- operated calcium entry in KO compared to WT. However,levels of [Ca 2+]cyto during tetanic stimulation were not modulated to variations ofextracellular calcium.Conclusions: The model-based analysis of experimentally determined calciumdistribution during tetanic stimulation showed that mitochondria can act as abuffer to compensate for the lack of PV. This result contributes to a better under-standing of mitochondria's role in modulating [Ca2+]cyto in skeletal muscle fibers.</dc:description><dc:date>2024</dc:date><dc:date>2024-11-13 11:20:42</dc:date><dc:type>Neznano</dc:type><dc:identifier>20828</dc:identifier><dc:language>sl</dc:language><dc:rights>© 2024 The Author(s)</dc:rights></rdf:Description></rdf:RDF>
