Profilin2 regulates actin rod assembly in neuronal cells

Nuclear and cytoplasmic actin-cofilin rods are formed transiently under stress conditions to reduce actin filament turnover and ATP hydrolysis. The persistence of these structures has been implicated in disease pathology of several neurological disorders. Recently, the presence of actin rods has been discovered in Spinal Muscular Atrophy (SMA), a neurodegenerative disease affecting predominantly motoneurons leading to muscle weakness and atrophy. This finding underlined the importance of dysregulated actin dynamics in motoneuron loss in SMA. In this study, we characterized actin rods formed in a SMA cell culture model analyzing their composition by LC-MS-based proteomics. Besides actin and cofilin, we identified proteins involved in processes such as ubiquitination, translation or protein folding to be bound to actin rods. This suggests their sequestration to actin rods, thus impairing important cellular functions. Moreover, we showed the involvement of the cytoskeletal protein profilin2 and its upstream effectors RhoA/ROCK in actin rod assembly in SMA. These findings implicate that the formation of actin rods exerts detrimental effects on motoneuron homeostasis by affecting actin dynamics and disturbing essential cellular pathways.

Automated summary

Under stress conditions, nuclear and cytoplasmic actin-cofilin rods are transiently formed to reduce actin filament turnover and ATP hydrolysis. The presence of actin rods in Spinal Muscular Atrophy (SMA) highlights the importance of dysregulated actin dynamics in motoneuron loss. Analysis of the composition of actin rods in a SMA cell culture model revealed binding of proteins involved in ubiquitination, translation, and protein folding, suggesting sequestration of these proteins and impairment of essential cellular functions. Involvement of profilin2 and its upstream effectors RhoA/ROCK in actin rod assembly in SMA indicates detrimental effects on motoneuron homeostasis by affecting actin dynamics and disturbing essential cellular pathways.