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<dc:title>NCLX Protein, but Not LETM1, Mediates Mitochondrial Ca2+ Extrusion, Thereby Limiting Ca2+-induced NAD(P)H Production and Modulating Matrix Redox State</dc:title>
<dc:creator>De Marchi, Umberto</dc:creator>
<dc:creator>Santo Domingo Mayoral, Jaime</dc:creator>
<dc:creator>Castelbou, Cyril</dc:creator>
<dc:creator>Sekler, Israel</dc:creator>
<dc:creator>Wiederkehr, Andreas</dc:creator>
<dc:creator>Demaurex, Nicolas</dc:creator>
<dc:description>Producción Científica</dc:description>
<dc:description>Mitochondria capture and subsequently release Ca(2+) ions, thereby sensing and shaping cellular Ca(2+) signals. The Ca(2+) uniporter MCU mediates Ca(2+) uptake, whereas NCLX (mitochondrial Na/Ca exchanger) and LETM1 (leucine zipper-EF-hand-containing transmembrane protein 1) were proposed to exchange Ca(2+) against Na(+) or H(+), respectively. Here we study the role of these ion exchangers in mitochondrial Ca(2+) extrusion and in Ca(2+)-metabolic coupling. Both NCLX and LETM1 proteins were expressed in HeLa cells mitochondria. The rate of mitochondrial Ca(2+) efflux, measured with a genetically encoded indicator during agonist stimulations, increased with the amplitude of mitochondrial Ca(2+) ([Ca(2+)]mt) elevations. NCLX overexpression enhanced the rates of Ca(2+) efflux, whereas increasing LETM1 levels had no impact on Ca(2+) extrusion. The fluorescence of the redox-sensitive probe roGFP increased during [Ca(2+)]mt elevations, indicating a net reduction of the matrix. This redox response was abolished by NCLX overexpression and restored by the Na(+)/Ca(2+) exchanger inhibitor CGP37157. The [Ca(2+)]mt elevations were associated with increases in the autofluorescence of NAD(P)H, whose amplitude was strongly reduced by NCLX overexpression, an effect reverted by Na(+)/Ca(2+) exchange inhibition. We conclude that NCLX, but not LETM1, mediates Ca(2+) extrusion from mitochondria. By controlling the duration of matrix Ca(2+) elevations, NCLX contributes to the regulation of NAD(P)H production and to the conversion of Ca(2+) signals into redox changes.</dc:description>
<dc:date>2024-02-07T14:59:11Z</dc:date>
<dc:date>2024-02-07T14:59:11Z</dc:date>
<dc:date>2014</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>J Biol Chem., Jul 2014, vol. 289, n. 29, p. 20377-85.</dc:identifier>
<dc:identifier>0021-9258</dc:identifier>
<dc:identifier>https://uvadoc.uva.es/handle/10324/65923</dc:identifier>
<dc:identifier>10.1074/jbc.M113.540898</dc:identifier>
<dc:identifier>20377</dc:identifier>
<dc:identifier>29</dc:identifier>
<dc:identifier>20385</dc:identifier>
<dc:identifier>Journal of Biological Chemistry</dc:identifier>
<dc:identifier>289</dc:identifier>
<dc:language>spa</dc:language>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:publisher>Elsevier</dc:publisher>
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