Chronically stressed or stress-preconditioned neurons fail to maintain stress granule assembly

Abstract

Dysregulation of stress granules (SGs) and their resident proteins contributes to pathogenesis of a number of (neuro)degenerative diseases. Phosphorylation of eIF2μ is an event integrating different types of cellular stress and it is required for SG assembly. Phosphorylated eIF2μ (p-eIF2μ) is upregulated in the nervous system in some neurodegenerative conditions. We found that increasing p-eIF2μ level by proteasomal inhibition in cultured cells, including mouse and human neurons, before a SG-inducing stress ('stress preconditioning'), limits their ability to maintain SG assembly. This is due to upregulation of PP1 phosphatase regulatory subunits GADD34 and/or CReP in preconditioned cells and early decline of p-eIF2μ levels during subsequent acute stress. In two model systems with constitutively upregulated p-eIF2μ, mouse embryonic fibroblasts lacking CReP and brain neurons of tau transgenic mice, SG formation was also impaired. Thus, neurons enduring chronic stress or primed by a transient mild stress fail to maintain p-eIF2μ levels following subsequent acute stress, which would compromise protective function of SGs. Our findings provide experimental evidence on possible loss of function for SGs in certain neurodegenerative diseases.