LETM1-Mediated K(+) and Na(+) Homeostasis Regulates Mitochondrial Ca(2+) Efflux

Ca(2+) transport across the inner membrane of mitochondria (IMM) is of major importance for their functions in bioenergetics, cell death and signaling. It is therefore tightly regulated. It has been recently proposed that LETM1—an IMM protein with a crucial role in mitochondrial K(+)/H(+) exchange and volume homeostasis—also acts as a Ca(2+)/H(+) exchanger. Here we show for the first time that lowering LETM1 gene expression by shRNA hampers mitochondrial K(+)/H(+) and Na(+)/H(+) exchange. Decreased exchange activity resulted in matrix K(+) accumulation in these mitochondria. Furthermore, LETM1 depletion selectively decreased Na(+)/Ca(2+) exchange mediated by NCLX, as observed in the presence of ruthenium red, a blocker of the Mitochondrial Ca(2+) Uniporter (MCU). These data confirm a key role of LETM1 in monovalent cation homeostasis, and suggest that the effects of its modulation on mitochondrial transmembrane Ca(2+) fluxes may reflect those on Na(+)/H(+) exchange activity.