Opposing roles of p38α-mediated phosphorylation and PRMT1-mediated arginine methylation in driving TDP-43 proteinopathy

Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disorder typically characterized by insoluble inclusions of hyperphosphorylated TDP-43. The mechanisms underlying toxic TDP-43 accumulation are not understood. Persistent activation of p38 mitogen-activated protein kinase (MAPK) is implicated in ALS. However, it is unclear how p38 MAPK affects TDP-43 proteinopathy. Here, we show that p38α MAPK inhibition reduces pathological TDP-43 phosphorylation, aggregation, cytoplasmic mislocalization, and neurotoxicity. Remarkably, p38α MAPK inhibition mitigates aberrant TDP-43 phenotypes in diverse ALS patient-derived motor neurons. p38α MAPK phosphorylates TDP-43 at pathological S409/S410 and S292, which reduces TDP-43 liquid-liquid phase separation (LLPS) but allows pathological TDP-43 aggregation. Moreover, we establish that PRMT1 methylates TDP-43 at R293. Importantly, S292 phosphorylation reduces R293 methylation, and R293 methylation reduces S409/S410 phosphorylation. Notably, R293 methylation permits TDP-43 LLPS and reduces pathological TDP-43 aggregation. Thus, strategies to reduce p38α-mediated TDP-43 phosphorylation and promote PRMT1-mediated R293 methylation could have therapeutic utility for ALS and related TDP-43 proteinopathies. [Display omitted] •p38α inhibition reduces aberrant TDP-43 phenotypes in patient-derived motor neurons•p38α phosphorylates TDP-43 at S292 and S409/S410, reducing LLPS but not aggregation•PRMT1 methylates TDP-43 at R293, reducing TDP-43 aggregation but not LLPS•Antagonistic TDP-43 methylation and phosphorylation suggest therapeutic strategies In this study, Aikio et al. establish opposing roles for p38α-mediated TDP-43 phosphorylation and PRMT1-mediated TDP-43 arginine methylation in driving TDP-43 proteinopathy. These findings suggest therapeutic strategies for ALS and related TDP-43 proteinopathies.