Cytoplasmic accumulation and aggregation of TDP-43 upon proteasome inhibition in cultured neurons

Janet van Eersel, Yazi D. Ke, Amadeus Gladbach, Mian Bi, Jürgen Götz, Jillian J. Kril, Lars M. Ittner

Research output: Contribution to journalArticle

65 Citations (Scopus)

Abstract

Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) are characterized by intraneuronal deposition of the nuclear TAR DNA-binding protein 43 (TDP-43) caused by unknown mechanisms. Here, we studied TDP-43 in primary neurons under different stress conditions and found that only proteasome inhibition by MG-132 or lactacystin could induce significant cytoplasmic accumulation of TDP-43, a histopathological hallmark in disease. This cytoplasmic accumulation was accompanied by phosphorylation, ubiquitination and aggregation of TDP-43, recapitulating major features of disease. Proteasome inhibition produced similar effects in both hippocampal and cortical neurons, as well as in immortalized motor neurons. To determine the contribution of TDP-43 to cell death, we reduced TDP-43 expression using small interfering RNA (siRNA), and found that reduced levels of TDP-43 dose-dependently rendered neurons more vulnerable to MG-132. Taken together, our data suggests a role for the proteasome in subcellular localization of TDP-43, and possibly in disease.

Original languageEnglish
Article numbere22850
Pages (from-to)1-13
Number of pages13
JournalPLoS ONE
Volume6
Issue number7
DOIs
Publication statusPublished - 3 Aug 2011
Externally publishedYes

Fingerprint Dive into the research topics of 'Cytoplasmic accumulation and aggregation of TDP-43 upon proteasome inhibition in cultured neurons'. Together they form a unique fingerprint.

Cite this