SUN1 facilitates CHMP7 nuclear influx and injury cascades in sporadic amyotrophic lateral sclerosis

We have recently identified the aberrant nuclear accumulation of the ESCRT-III protein CHMP7 as an initiating event that leads to a significant injury to the nuclear pore complex (NPC) characterized by the reduction of specific nucleoporins from the neuronal NPC in sporadic amyotrophic lateral sclerosis (sALS) and C9orf72 ALS/frontotemporal dementia (FTD)-induced pluripotent stem cell-derived neurons (iPSNs), a phenomenon also observed in post-mortem patient tissues. Importantly, this NPC injury is sufficient to contribute to TDP-43 dysfunction and mislocalization, a common pathological hallmark of neurodegenerative diseases. However, the molecular mechanisms and events that give rise to increased nuclear translocation and/or retention of CHMP7 to initiate this pathophysiological cascade remain largely unknown. Here, using an iPSN model of sALS, we demonstrate that impaired NPC permeability barrier integrity and interactions with the LINC complex protein SUN1 facilitate CHMP7 nuclear localization and the subsequent 'activation' of NPC injury cascades. Collectively, our data provide mechanistic insights in the pathophysiological underpinnings of ALS/FTD and highlight SUN1 as a potent contributor to and modifier of CHMP7-mediated toxicity in sALS pathogenesis. Using iPSC-derived neurons from patients with sporadic ALS, Baskerville et al. show that defects in nuclear-cytoplasmic cellular compartmentalization and specific nuclear membrane proteins trigger a nuclear influx of CHMP7. This in turn initiates nuclear pore complex injury cascades implicated in ALS pathogenesis.

Automated summary

Researchers have found that defects in nuclear-cytoplasmic cellular compartmentalization and specific nuclear membrane proteins trigger the nuclear accumulation of CHMP7 in patients with sporadic amyotrophic lateral sclerosis (sALS), leading to a cascade of nuclear pore complex injury implicated in ALS pathogenesis.