Stress granules inhibit fatty acid oxidation by modulating mitochondrial permeability

Amen, Triana and Kaganovich, Daniel (2021) Stress granules inhibit fatty acid oxidation by modulating mitochondrial permeability. Cell Reports, 35 (11), [109237]. (doi:10.1016/j.celrep.2021.109237).

Abstract

The formation of stress granules (SGs) is an essential aspect of the cellular response to many kinds of stress, but its adaptive role is far from clear. SG dysfunction is implicated in aging-onset neurodegenerative diseases, prompting interest in their physiological function. Here, we report that during starvation stress, SGs interact with mitochondria and regulate metabolic remodeling. We show that SG formation leads to a downregulation of fatty acid β-oxidation (FAO) through the modulation of mitochondrial voltage-dependent anion channels (VDACs), which import fatty acids (FAs) into mitochondria. The subsequent decrease in FAO during long-term starvation reduces oxidative damage and rations FAs for longer use. Failure to form SGs, whether caused by the genetic deletion of SG components or an amyotrophic lateral sclerosis (ALS)-associated mutation, translates into an inability to downregulate FAO. Because metabolic dysfunction is a common pathological element of neurodegenerative diseases, including ALS, our findings provide a direction for studying the clinical relevance of SGs.

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Contributors

Author: Triana Amen

Author: Daniel Kaganovich

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