GSAP regulates lipid homeostasis and mitochondrial function associated with Alzheimer's disease Journal Article


Authors: Xu, P.; Chang, J. C.; Zhou, X.; Wang, W.; Bamkole, M.; Wong, E.; Bettayeb, K.; Jiang, L. L.; Huang, T.; Luo, W.; Xu, H.; Nairn, A. C.; Flajolet, M.; Ip, N. Y.; Li, Y. M.; Greengard, P.
Article Title: GSAP regulates lipid homeostasis and mitochondrial function associated with Alzheimer's disease
Abstract: Biochemical, pathogenic, and human genetic data confirm that GSAP (γ-secretase activating protein), a selective γ-secretase modulatory protein, plays important roles in Alzheimer's disease (AD) and Down's syndrome. However, the molecular mechanism(s) underlying GSAP-dependent pathogenesis remains largely elusive. Here, through unbiased proteomics and single-nuclei RNAseq, we identified that GSAP regulates multiple biological pathways, including protein phosphorylation, trafficking, lipid metabolism, and mitochondrial function. We demonstrated that GSAP physically interacts with the Fe65-APP complex to regulate APP trafficking/partitioning. GSAP is enriched in the mitochondria-associated membrane (MAM) and regulates lipid homeostasis through the amyloidogenic processing of APP. GSAP deletion generates a lipid environment unfavorable for AD pathogenesis, leading to improved mitochondrial function and the rescue of cognitive deficits in an AD mouse model. Finally, we identified a novel GSAP single-nucleotide polymorphism that regulates its brain transcript level and is associated with an increased AD risk. Together, our findings indicate that GSAP impairs mitochondrial function through its MAM localization and that lowering GSAP expression reduces pathological effects associated with AD. © 2021 Xu et al.
Journal Title: Journal of Experimental Medicine
Volume: 218
Issue: 8
ISSN: 0022-1007
Publisher: Rockefeller University Press  
Date Published: 2021-08-02
Start Page: e20202446
Language: English
DOI: 10.1084/jem.20202446
PUBMED: 34156424
PROVIDER: scopus
PMCID: PMC8222926
DOI/URL:
Notes: Article -- Export Date: 2 August 2021 -- Source: Scopus
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  1. Yueming Li
    132 Li
  2. Jerry C Chang
    3 Chang
  3. Wan Fung Wong
    12 Wong