ALS/FTD mutant CHCHD10 mice reveal a tissue-specific toxic gain-of-function and mitochondrial stress response.

Abstract

Mutations in coiled-coil-helix-coiled-coil-helix domain containing 10 (CHCHD10), a mitochondrial protein of unknown function, cause a disease spectrum with clinical features of motor neuron disease, dementia, myopathy and cardiomyopathy. To investigate the pathogenic mechanisms of CHCHD10, we generated mutant knock-in mice harboring the mouse-equivalent of a disease-associated human S59L mutation, S55L in the endogenous mouse gene. CHCHD10S55L mice develop progressive motor deficits, myopathy, cardiomyopathy and accelerated mortality. Critically, CHCHD10 accumulates in aggregates with its paralog CHCHD2 specifically in affected tissues of CHCHD10S55L mice, leading to aberrant organelle morphology and function. Aggregates induce a potent mitochondrial integrated stress response (mtISR) through mTORC1 activation, with elevation of stress-induced transcription factors, secretion of myokines, upregulated serine and one-carbon metabolism, and downregulation of respiratory chain enzymes. Conversely, CHCHD10 ablation does not induce disease pathology or activate the mtISR, indicating that CHCHD10S55L-dependent disease pathology is not caused by loss-of-function. Overall, CHCHD10S55L mice recapitulate crucial aspects of human disease and reveal a novel toxic gain-of-function mechanism through maladaptive mtISR and metabolic dysregulation.

• Authors: Corey J Anderson, Kirsten Bredvik, Suzanne R Burstein, Crystal Davis, Samantha M Meadows, Jalia Dash, Laure Case, Teresa A Milner, Hibiki Kawamata, Aamir Zuberi, Alessandra Piersigilli, Cathleen Lutz, Giovanni Manfredi
• Journal: Acta neuropathologica (Acta Neuropathol) Vol. 138 Issue 1 Pg. 103-121 (07 2019) ISSN: 1432-0533 [Electronic] Germany
• PMID: 30877432 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Topics

• Animals
• Frontotemporal Dementia (genetics, pathology)
• Gain of Function Mutation (genetics)
• Genetic Association Studies
• Mice, Transgenic
• Mitochondria (genetics, pathology)
• Mitochondrial Membranes (metabolism)
• Mutation (genetics)
• Parkinson Disease (genetics)