Neuronal Overexpression of HTDP-43 in Mimics the Cellular Pathology Commonly Observed in TDP-43 Proteinopathies
Overview
Affiliations
Inclusions consisting of transactive response DNA-binding protein 43 (TDP-43) are a characteristic feature of amyotrophic lateral sclerosis (ALS). has been instrumental in studying the underlying mechanisms of TDP-43 pathology. Here, we extend the possibilities of previous studies by examining a model expressing human wild-type ( ) pan-neuronally. We show that disease-related (hyper)phosphorylation and cytosolic localisation of hTDP-43 are present in hTDP-43 worms and that these features can be enhanced by adjusting the environmental temperature.
Eck R, Stair J, Kraemer B, Liachko N Front Neurosci. 2024; 17:1300705.
PMID: 38239833 PMC: 10794587. DOI: 10.3389/fnins.2023.1300705.
Neuronal overexpression of hTDP-43 in impairs motor function.
Koopman M, Gungordu L, Seinstra R, Nollen E MicroPubl Biol. 2023; 2023.
PMID: 37159576 PMC: 10163325. DOI: 10.17912/micropub.biology.000768.
Neuronal overexpression of human TDP-43 in causes a range of sensorimotor phenotypes.
Koopman M, Gungordu L, Seinstra R, Nollen E MicroPubl Biol. 2023; 2023.
PMID: 37151213 PMC: 10157381. DOI: 10.17912/micropub.biology.000766.