Enhanced mGluR₅ intracellular activity causes psychiatric alterations in Niemann Pick type C disease.

ABSTRACT: Niemann-Pick disease Type C (NPC) is caused by mutations in the cholesterol transport protein NPC1 leading to the endolysosomal accumulation of the lipid and to psychiatric alterations. Using an NPC mouse model (Npc1^nmf164) we show aberrant mGluR₅ lysosomal accumulation and reduction at plasma membrane in NPC1 deficient neurons. This phenotype was induced in wild-type (wt) neurons by genetic and pharmacological NPC1 silencing. Extraction of cholesterol normalized mGluR₅ distribution in NPC1-deficient neurons. Intracellular accumulation of mGluR₅ was functionally active leading to enhanced mGluR-dependent long-term depression (mGluR-LTD) in Npc1^nmf164 hippocampal slices. mGluR-LTD was lower or higher in Npc1^nmf164 slices comp

SUBMITTER: Toledano-Zaragoza A 

PROVIDER: S-EPMC11499878 | biostudies-literature | 2024 Oct

REPOSITORIES: biostudies-literature