Temporary alteration of neuronal network communication is a protective response to redox imbalance that requires GPI-anchored prion protein

• Published in: Redox biology Vol. 63; p. 102733
• Main Authors: Foliaki, Simote T., Wood, Aleksandar, Williams, Katie, Smith, Anna, Walters, Ryan O., Baune, Chase, Groveman, Bradley R., Haigh, Cathryn L.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01-07-2023; Elsevier
• Subjects: Animals; Disease Models, Animal; Hippocampal CA1 long-term potentiation; Mice; Neuronal cytoskeleton; Neuronal network communication; Neurons - metabolism; Oxidation-Reduction; Oxidative stress; Prion disease; Prion Diseases; Prion protein; Prion Proteins - genetics; Prion Proteins - metabolism; Prions - metabolism; PrP; Research Paper; Synaptic Transmission; Oxidative stress; Prion disease; Synaptic transmission; Neuronal network communication; Prion protein; PrP; Neuronal cytoskeleton; Hippocampal CA1 long-term potentiation
• ISSN: 2213-2317; 2213-2317
• DOI: 10.1016/j.redox.2023.102733

Cellular prion protein (PrPC) protects neurons against oxidative stress damage. This role is lost upon its misfolding into insoluble prions in prion diseases, and correlated with cytoskeletal breakdown and neurophysiological deficits. Here we used mouse neuronal models to assess how PrPC protects the neuronal cytoskeleton, and its role in network communication, from oxidative stress damage. Oxidative stress was induced extrinsically by potassium superoxide (KO2) or intrinsically by Mito-Paraquat (MtPQ), targeting the mitochondria. In mouse neural lineage cells, KO2 was damaging to the cytoskeleton, with cells lacking PrPC (PrP-/-) damaged more than wild-type (WT) cells. In hippocampal slices, KO2 acutely inhibited neuronal communication in WT controls without damaging the cytoskeleton. This inhibition was not observed in PrP-/- slices. Neuronal communication and the cytoskeleton of PrP-/- slices became progressively disrupted and degenerated post-recovery, whereas the dysfunction in WT slices recovered in 5 days. This suggests that the acute inhibition of neuronal activity in WT slices in response to KO2 was a neuroprotective role of PrPC, which PrP-/- slices lacked. Heterozygous expression of PrPC was sufficient for this neuroprotection. Further, hippocampal slices from mice expressing PrPC without its GPI anchor (PrPGPI-/-) displayed acute inhibition of neuronal activity by KO2. However, they failed to restore normal activity and cytoskeletal formation post-recovery. This suggests that PrPC facilitates the depressive response to KO2 and its GPI anchoring is required to restore KO2-induced damages. Immuno spin-trapping showed increased radicals formed on the filamentous actin of PrP-/- and PrPGPI-/- slices, but not WT and PrP+/- slices, post-recovery suggesting ongoing dysregulation of redox balance in the slices lacking GPI-anchored PrPC. The MtPQ treatment of hippocampal slices temporarily inhibited neuronal communication independent of PrPC expression. Overall, GPI-anchored PrPC alters synapses and neurotransmission to protect and repair the neuronal cytoskeleton, and neuronal communication, from extrinsically induced oxidative stress damages.