Author:
Assoni Amanda Faria,Guerrero Erika N.,Wardenaar René,Oliveira Danyllo,Bakker Petra L.,Carvalho Valdemir Melechco,Okamoto Oswaldo Keith,Zatz Mayana,Foijer Floris
Abstract
AbstractAmyotrophic lateral sclerosis type 6 (ALS6) is a familial subtype of ALS linked to Fused in Sarcoma (FUS) gene mutation. FUS mutations lead to decreased global protein synthesis, but the mechanism that drives this has not been established. Here, we used ALS6 patient-derived induced pluripotent stem cells (hIPSCs) to study the effect of the ALS6 FUSR521Hmutation on the translation machinery in motor neurons (MNs). We find, in agreement with findings of others, that protein synthesis is decreased in ALS6 MNs. Furthermore, ALS6 MNs are more sensitive to oxidative stress and display reduced expression of TGF-β and mTORC gene pathways when stressed. Finally, we show that IFNγtreatment reduces apoptosis of ALS6 MNs exposed to oxidative stress and partially restores the translation rates in ALS6 MNs. Overall, these findings suggest that a functional IFNγresponse is important for FUS-mediated protein synthesis, possibly by FUS nuclear translocation in ALS6.Highlights and eTOC blurbALS6 patient-derived motor neurons show decreased viability and reduced production of innate immune cytokines following oxidative stressFUS cytoplasmic localization coincides with decreased protein synthesis ratesIFNγtreatment of ALS6 patient-derived motor neurons reduces apoptosis and ameliorates translation rates resulting from oxidative stress
Publisher
Cold Spring Harbor Laboratory