Up-regulation of cholesterol synthesis by lysosomal defects requires a functional mitochondrial respiratory chain
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ABSTRACT: To understand the common and opposite effects of mitochondrial and lysosomal perturbations on cellular signaling, we performed RNAseq in HeLa cells stably silenced for the mitochondrial respiratory chain subunit UQCRC1 (as a model of chronic mitochondrial respiratory chain deficiency), for lysosomal hydrolase acid alpla-glucosidase (GAA), or for lysosomal cathepsin B (CTSB). The controls were HeLa cells with scrambled shRNA.
ORGANISM(S): Homo sapiens
PROVIDER: GSE256471 | GEO | 2024/05/24
REPOSITORIES: GEO
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