Research Grant from the Hungarian Academy of Sciences(LP2016-4/2016)
European Research Council Grant ERC-CoG(724994)
Szakterületek:
Általános orvostudomány
Egyéb orvostudományok
Klinikai orvostan
Mitochondrial function in neurons is tightly linked with metabolic and signaling mechanisms
that ultimately determine neuronal performance. The subcellular distribution of these
organelles is dynamically regulated as they are directed to axonal release sites on
demand, but whether mitochondrial internal ultrastructure and molecular properties
would reflect the actual performance requirements in a synapse-specific manner, remains
to be established. Here, we examined performance-determining ultrastructural features
of presynaptic mitochondria in GABAergic and glutamatergic axons of mice and human.
Using electron-tomography and super-resolution microscopy we found, that these features
were coupled to synaptic strength: mitochondria in boutons with high synaptic activity
exhibited an ultrastructure optimized for high rate metabolism and contained higher
levels of the respiratory chain protein cytochrome-c (CytC) than mitochondria in boutons
with lower activity. The strong, cell type-independent correlation between mitochondrial
ultrastructure, molecular fingerprints and synaptic performance suggests that changes
in synaptic activity could trigger ultrastructural plasticity of presynaptic mitochondria,
likely to adjust their performance to the actual metabolic demand.