CHCHD10 and SLP2 control the stability of the PHB complex: a key factor for motor neuron viability

Genin et al. show that the mitochondrial proteins SLP2 and prohibitins are part of the pathological cascade through which the p.Ser59Leu variant of CHCHD10 gives rise to ALS. Aggregates of SLP2/prohibitins and instability of the PHB complex in the inner mitochondrial membrane lead to mitochondrial fragmentation and cell death. CHCHD10 is an amyotrophic lateral sclerosis/frontotemporal dementia gene that encodes a mitochondrial protein whose precise function is unclear. Here we show that Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing protein 10 interacts with the Stomatin-Like Protein 2 and participates in the stability of the prohibitin complex in the inner mitochondrial membrane. By using patient fibroblasts and mouse models expressing the same CHCHD10 variant (p.Ser59Leu), we show that Stomatin-Like Protein 2 forms aggregates with prohibitins, found in vivo in the hippocampus and as aggresome-like inclusions in spinal motor neurons of Chchd10(S59L/+) mice. Affected cells and tissues display instability of the prohibitin complex, which participates at least in part in the activation of the OMA1 cascade with OPA1 processing leading to mitochondrial fragmentation, abnormal mitochondrial cristae morphogenesis and neuronal death found in spinal cord and the hippocampus of Chchd10(S59L/+) animals. Destabilization of the prohibitin complex leads to the instability of the mitochondrial contact site and cristae organizing the system complex, probably by the disruption of OPA1-mitofilin interaction. Thus, Stomatin-Like Protein 2/prohibitin aggregates and destabilization of the prohibitin complex are critical in the sequence of events leading to motor neuron death in CHCHD10(S59L)-related disease.

Automated summary

Genin et al. show that SLP2 and prohibitins play a role in the pathological cascade of ALS caused by the p.Ser59Leu variant of CHCHD10. Aggregates of SLP2/prohibitins and instability of the PHB complex result in mitochondrial fragmentation and cell death.