Remodeling of Liver and Plasma Lipidomes in Mice Lacking Cyclophilin D

• Published in: International journal of molecular sciences 2022-09, Vol.23 (19), p.11274
• Main Authors: Koszegi, Balazs, Balogh, Gabor, Berente, Zoltan, Vranesics, Anett, Pollak, Edit, Molnar, Laszlo, Takatsy, Aniko, Poor, Viktoria, Wahr, Matyas, Antus, Csenge, Eros, Krisztian, Vigh, Laszlo, Gallyas, Jr, Ferenc, Peter, Maria, Veres, Balazs
• Format: Article
• Language: English
• Subjects: Ablation; Animals; cyclophilin D; Cyclophilins - genetics; Cyclophilins - metabolism; Discriminant analysis; Electron microscopy; Fat metabolism; Fatty acids; Glucose; Glucose metabolism; Hepatocytes; High fat diet; Histochemistry; Lipid composition; Lipid metabolism; Lipidomics; Lipids; Liver; Liver - metabolism; Long-term effects; Magnetic resonance imaging; Membrane Lipids; Membrane permeability; Metabolic pathways; Metabolism; Mice; Mice, Knockout; Mitochondria; Mitochondrial Membrane Transport Proteins - metabolism; Mitochondrial permeability transition pore; NMR; Nuclear magnetic resonance; Peptidyl-Prolyl Isomerase F; Plasma; Ultrastructure
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms231911274

In recent years, several studies aimed to investigate the metabolic effects of non-functioning or absent cyclophilin D (CypD), a crucial regulatory component of mitochondrial permeability transition pores. It has been reported that the lack of CypD affects glucose and lipid metabolism. However, the findings are controversial regarding the metabolic pathways involved, and most reports describe the effect of a high-fat diet on metabolism. We performed a lipidomic analysis of plasma and liver samples of CypD-/- and wild-type (WT) mice to reveal the lipid-specific alterations resulting from the absence of CypD. In the CypD-/- mice compared to the WT animals, we found a significant change in 52% and 47% of the measured 225 and 201 lipid species in liver and plasma samples, respectively. The higher total lipid content detected in these tissues was not accompanied by abdominal fat accumulation assessed by nuclear magnetic resonance imaging. We also documented characteristic changes in the lipid composition of the liver and plasma as a result of CypD ablation with the relative increase in polyunsaturated membrane lipid species. In addition, we did not observe remarkable differences in the lipid distribution of hepatocytes using histochemistry, but we found characteristic changes in the hepatocyte ultrastructure in CypD-/- animals using electron microscopy. Our results highlight the possible long-term effects of CypD inhibition as a novel therapeutic consideration for various diseases.