Hyperactive somatostatin interneurons contribute to excitotoxicity in neurodegenerative disorders.

ABSTRACT: Amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are overlapping neurodegenerative disorders whose pathogenesis remains largely unknown. Using TDP-43(A315T) mice, an ALS and FTD model with marked cortical pathology, we found that hyperactive somatostatin interneurons disinhibited layer 5 pyramidal neurons (L5-PNs) and contributed to their excitotoxicity. Focal ablation of somatostatin interneurons efficiently restored normal excitability of L5-PNs and alleviated neurodegeneration, suggesting a new therapeutic target for ALS and FTD.

SUBMITTER: Zhang W 

PROVIDER: S-EPMC4811704 | biostudies-literature | 2016 Apr

REPOSITORIES: biostudies-literature