Neurodegenerative disorders such as Alzheimer’s disease (AD) and Parkinson’s disease
(PD) are characterized by the accumulation of misfolded proteins in the endoplasmic reticulum (ER)
and the unfolded protein response (UPR). Modulating the UPR is one of the major challenges to
counteract the development of neurodegenerative disorders and other diseases with affected UPR.
Here, we show that miR-34a-5p directly targets the IRE1α branch of the UPR, including the genes BIP,
IRE1α, and XBP1. Upon induction of ER stress in neuronal cells, miR-34a-5p overexpression impacts
the resulting UPR via a significant reduction in IRE1α and XBP1s that in turn leads to decreased
viability, increased cytotoxicity and caspase activity. The possibility to modify the UPR signaling
pathway by a single miRNA that targets central genes of the IRE1α branch offers new perspectives
for future therapeutic approaches against neurodegeneration
