Metabolic reprogramming of hepatocytes by Schistosoma mansoni eggs

Schistosomiasis is a parasitic infection which affects more than 200 million people globally. Schistosome eggs, but not the adult worms, are mainly responsible for schistosomiasis-specific morbidity in the liver. It is unclear if S. mansoni eggs consume host metabolites, and how this compromises the...

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Veröffentlicht in:JHEP reports 2023-02, Vol.5 (2), p.100625-100625, Article 100625
Hauptverfasser: von Bülow, Verena, Gindner, Sarah, Baier, Anne, Hehr, Laura, Buss, Nicola, Russ, Lena, Wrobel, Sarah, Wirth, Victoria, Tabatabai, Kuscha, Quack, Thomas, Haeberlein, Simone, Kadesch, Patrik, Gerbig, Stefanie, Wiedemann, Katja R., Spengler, Bernhard, Mehl, Annabel, Morlock, Gertrud, Schramm, Gabriele, Pons-Kühnemann, Jörn, Falcone, Franco H., Wilson, R. Alan, Bankov, Katrin, Wild, Peter, Grevelding, Christoph G., Roeb, Elke, Roderfeld, Martin
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Sprache:eng
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Zusammenfassung:Schistosomiasis is a parasitic infection which affects more than 200 million people globally. Schistosome eggs, but not the adult worms, are mainly responsible for schistosomiasis-specific morbidity in the liver. It is unclear if S. mansoni eggs consume host metabolites, and how this compromises the host parenchyma. Metabolic reprogramming was analyzed by matrix-assisted laser desorption/ionization mass spectrometry imaging, liquid chromatography with high-resolution mass spectrometry, metabolite quantification, confocal laser scanning microscopy, live cell imaging, quantitative real-time PCR, western blotting, assessment of DNA damage, and immunohistology in hamster models and functional experiments in human cell lines. Major results were validated in human biopsies. The infection with S. mansoni provokes hepatic exhaustion of neutral lipids and glycogen. Furthermore, the distribution of distinct lipid species and the regulation of rate-limiting metabolic enzymes is disrupted in the liver of S. mansoni infected animals. Notably, eggs mobilize, incorporate, and store host lipids, while the associated metabolic reprogramming causes oxidative stress-induced DNA damage in hepatocytes. Administration of reactive oxygen species scavengers ameliorates these deleterious effects. Our findings indicate that S. mansoni eggs completely reprogram lipid and carbohydrate metabolism via soluble factors, which results in oxidative stress-induced cell damage in the host parenchyma. The authors demonstrate that soluble egg products of the parasite S. mansoni induce hepatocellular reprogramming, causing metabolic exhaustion and a strong redox imbalance. Notably, eggs mobilize, incorporate, and store host lipids, while the metabolic reprogramming causes oxidative stress-induced DNA damage in hepatocytes, independent of the host's immune response. S. mansoni eggs take advantage of the host environment through metabolic reprogramming of hepatocytes and enterocytes. By inducing DNA damage, this neglected tropical disease might promote hepatocellular damage and thus influence international health efforts. [Display omitted] •S. mansoni soluble egg products induce hepatocellular metabolic reprogramming.•S. mansoni eggs mobilize, incorporate, and store host lipids.•S. mansoni provoke parenchymal reprogramming and cause metabolic exhaustion in the liver.•S. mansoni eggs prompt a metabolic crisis-associated redox imbalance and provoke DNA damage.•S. mansoni eggs induce processes that
ISSN:2589-5559
2589-5559
DOI:10.1016/j.jhepr.2022.100625