The unfolded protein response in models of human mutant G93A amyotrophic lateral sclerosis

T. Prell*, J. Lautenschläger, O. W. Witte, M. T. Carri, J. Grosskreutz

*Corresponding author for this work
32 Citations (Scopus)


Recent studies indicate that endoplasmic reticulum (ER) stress is involved in the pathogenesis of familial and sporadic amyotrophic lateral sclerosis (ALS). ER stress occurs when the ER-mitochondria calcium cycle (ERMCC) is disturbed and misfolded proteins accumulate in the ER. To cope with ER stress, the cell engages the unfolded protein response (UPR). While activation of the UPR has been shown in some ALS models and tissues, ER stress elements have not been studied directly in motor neurons. Here we investigated the expression of XBP1 and ATF6α and phosphorylation of eIF2α, and their modulation, in mutated SOD1 G93A NSC34 and animal model of ALS. Expression of XBP1 and ATF6α mRNA and protein was enhanced in SOD1 G93A NSC34 cells. Activation of ATF6α and XBP1 and phosphorylation of eIF2α were detectable in mutated SOD1 G93A motor but not in wild-type motor neurons. Treatment with the ER stressor thapsigargin enhanced phosphorylation of eIF2α and activated proteolysis of ATF6α and splicing of XBP1 in NSC34 and motor neurons in a time-dependent manner. The present study thus provides direct evidence of activated UPR in motor neurons which overexpress human pathogenic mutant SOD1 G93A, providing evidence that ER stress plays a major role in ALS.

Original languageEnglish
JournalEuropean Journal of Neuroscience
Issue number5
Pages (from-to)652-660
Number of pages9
Publication statusPublished - 03.2012
Externally publishedYes

Research Areas and Centers

  • Centers: Center for Neuromuscular Diseases


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