G37R SOD1 mutant alters mitochondrial complex I activity, Ca²⁺ uptake and ATP production
2011
Coussee, Evelyne | De Smet, Patrick | Bogaert, Elke | Elens, Iris | Van Damme, Philip | Willems, Peter | Koopman, Werner | Van Den Bosch, Ludo | Callewaert, Geert
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease characterized by selective death of motor neurons. Mutations in Cu/Zn superoxide dismutase-1 (SOD1) cause familial ALS but the molecular mechanisms whereby these mutations induce motor neuron death remain controversial. Here, we show that stable overexpression of mutant human SOD1 (G37R) – but not wild-type SOD1 (wt-SOD1) – in mouse neuroblastoma cells (N2a) results in morphological abnormalities of mitochondria accompanied by several dysfunctions. Activity of the oxidative phosphorylation complex I was significantly reduced in G37R cells and correlated with lower mitochondrial membrane potential and reduced levels of cytosolic ATP. Using targeted chimeric aequorin we further analyzed the consequences of mitochondrial dysfunction on cellular Ca²⁺ handling. Mitochondrial Ca²⁺ uptake, elicited by IP₃-induced Ca²⁺ release from endoplasmic reticulum (ER) was significantly reduced in G37R cells, while uptake induced by a brief Ca²⁺ pulse was not affected in permeabilized cells. The decreased mitochondrial Ca²⁺ uptake resulted in increased cytosolic Ca²⁺ transients, whereas ER Ca²⁺ load and resting cytosolic Ca²⁺ levels were not affected. Together, these findings suggest that the mechanism linking mutant G37R SOD1 and ALS involves mitochondrial respiratory chain deficiency resulting in ATP loss and impairment of mitochondrial and cytosolic Ca²⁺ homeostasis.
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