Transcriptomics

Dataset Information

0

Neuronal ABCA7 deficiency aggravates mitochondrial dysfunction and neurodegeneration in Alzheimer’s disease [II]


ABSTRACT: Loss-of-function variants of the ABCA7 gene are associated with the increased risk of Alzheimer's disease (AD). How neuronal ABCA7 contributes to AD pathogenesis is unknown. Using neuron-specific Abca7 knockout mice (nAbca7−/−) with or without 5×FAD amyloid model background and postmortem AD brains, we investigated AD-related phenotypes through comprehensive approaches including transcriptomics and lipidomics. Lipidomics analysis detected altered lipid profiles in the brains and synaptosomes of 5×FAD; nAbca7−/− mice compared to controls. Transcriptomics profiling revealed that neuronal ABCA7 deficiency altered the expression of genes and pathways related to mitochondrial homeostasis and apoptosis, particularly in excitatory neurons. Consistently, synaptosomes isolated from 5×FAD; nAbca7−/− mice showed diminished mitochondria respiration and reduced synaptic protein levels, which are further supported by results from human AD brains. Our findings reveal that neuronal ABCA7 plays a critical role in mitochondrial homeostasis important for neuronal function and survival in the presence of AD pathology.

ORGANISM(S): Mus musculus

PROVIDER: GSE291092 | GEO | 2025/04/02

REPOSITORIES: GEO

Dataset's files

Source:
Action DRS
Other
Items per page:
1 - 1 of 1

Similar Datasets

2025-04-02 | GSE291086 | GEO
2025-04-02 | GSE291674 | GEO
2024-01-17 | GSE247360 | GEO
2025-03-13 | GSE288170 | GEO
2024-07-19 | GSE244550 | GEO
2019-10-31 | GSE139592 | GEO
| PRJNA1037158 | ENA
2023-11-13 | GSE239455 | GEO
| PRJEB29458 | ENA
2023-12-13 | PXD042905 | Pride