Dysregulation of lipid metabolism in the liver of Tspo knockout mice

Tools

Farhan, Fahad and Raghupathy, Rakesh Kotapati and Baran, Michal R. and Wong, Aileen and Biswas, Lincoln and Jiang, Hui-Rong and Craft, John A. and Shu, Xinhua (2025) Dysregulation of lipid metabolism in the liver of Tspo knockout mice. Biochimica et Biophysica Acta Molecular and Cell Biology of Lipids, 1870 (1). 159566. ISSN 1388-1981 (https://doi.org/10.1016/j.bbalip.2024.159566)

[thumbnail of Farhan-etal-BBAMCBL-2024-Dysregulation-of-lipid-metabolism-in-the-liver]
Preview
 Text. Filename: Farhan-etal-BBAMCBL-2024-Dysregulation-of-lipid-metabolism-in-the-liver.pdf
Final Published Version
License: Creative Commons Attribution 4.0 logo
Download (5MB)| Preview

Abstract

The translocator protein, TSPO, has been implicated in a wide range of cellular processes exerted from its position in the outer mitochondrial membrane from where it influences lipid metabolism and mitochondrial oxidative activity. Understanding how this protein regulates a profusion of processes requires further elucidation and to that end we have examined lipid metabolism and used an RNAseq strategy to compare transcript abundance in wildtype and Tspo knockout (KO) mouse liver. The levels of cholesterol, triglyceride and phospholipid were significantly elevated in the KO mouse liver. The expression of cholesterol homeostasis genes was markedly downregulated. Determination of the differential expression revealed that many genes were either up- or downregulated in the KO animals. However, a striking observation within the results was a decrease of transcripts for protein degradation proteins in KO animals while protease inhibitors were enriched. When the entire abundance data-set was analysed with CEMiTool, and revealed a module of proteins that were under-represented in the KO animals. These could subsequently be formed into a network comprising three interlinked clusters at the centre of which were proteins of cytoplasmic ribosomes with gene ontology terms suggesting impairment to translation. The largest cluster was dominated by proteins of lipid metabolism but also contained disparate systems of iron metabolism and behaviour. The third cluster was dominated by proteins of the electron transport chain and oxidative phosphorylation. These findings suggest that TSPO contributes to lipid metabolism, detoxification of active oxygen species and oxidative phosphorylation, and regulates mitochondrial retrograde signalling.

ORCID iDs

Farhan, Fahad, Raghupathy, Rakesh Kotapati, Baran, Michal R., Wong, Aileen, Biswas, Lincoln, Jiang, Hui-Rong ORCID logoORCID: https://orcid.org/0000-0002-5753-0091, Craft, John A. and Shu, Xinhua;
CORE (COnnecting REpositories)