Loss of hepatic Lgr4 and Lgr5 promotes nonalcoholic fatty liver disease

Saponara, E.; Penno, C.; Matadamas Guzman, M. L.; Brun, V.; Fischer, B.; Brousseau, M.; Wang, Z.-Y.; ODonnell, P.; Turner, J.; Graff Meyer, A.; Bollepalli, L.; dArio, G.; Roma, G.; Carbone, W.; Orsini, V.; Annunziato, S.; Obrecht, M.; Beckmann, N.; Saravanan, C.; Osmont, A.; Tropberger, P.; Richards, S.; Genoud, C.; Aebi, A.; Ley, S.; Ksiazek, I.; Nigsch, F.; Terraciano, L.; Bouwmeester, T.; Tchorz, J.; Ruffner, H.

doi:10.1101/2021.11.22.469602

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bioRxiv · 10.1101/2021.11.22.469602

Loss of hepatic Lgr4 and Lgr5 promotes nonalcoholic fatty liver disease

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Abstract

Background & AimsThe Rspo-Lgr4/5-Znrf3/Rnf43 module is a master regulator of hepatic Wnt/{beta}-catenin signaling and metabolic zonation, but its impact on nonalcoholic fatty liver disease (NAFLD) remains unclear. We studied whether liver-specific loss of the Wnt/{beta}-catenin modulators Leucine-Rich Repeat-Containing G Protein-Coupled Receptor 4/5 (Lgr4/5) promotes nonalcoholic fatty liver disease (NAFLD). MethodsMice with liver-specific deletion of both receptors Lgr4/5 (Lgr4/5dLKO) were fed with normal diet (ND) or high fat diet (HFD). Livers of these mice were analyzed for lipid and fibrotic content by tissue staining and immunohistochemistry (IHC), and lipoproteins, inflammation and liver enzyme markers were measured in blood. Mechanistic insights into hepatic lipid accumulation were obtained by using ex vivo primary hepatocyte cultures derived from the Lgr4/5dLKO mice. Lipid analysis of mouse livers was performed by mass spectrometry (MS)-based untargeted lipidomic analysis. ResultsWe demonstrated that liver-specific ablation of Lgr4/5-mediated Wnt signaling resulted in hepatic steatosis, impaired bile acid (BA) secretion and predisposition to liver fibrosis. Under HFD conditions, we observed progressive intrahepatic fat accumulation, developing into macro-vesicular steatosis. Serum lipoprotein levels in HFD-fed Lgr4/5dLKO mice were decreased, rather than increased, suggesting that accumulation of fat in the liver was due to impaired lipid secretion by hepatocytes. Our lipidome analysis revealed a severe alteration of several lipid species in livers of Lgr4/5dLKO mice, including triacylglycerol estolides (TG-EST), a storage form of bioactive free fatty acid (FA) esters of hydroxy FAs (FAHFAs). ConclusionsLoss of hepatic Wnt/{beta}-catenin activity by Lgr4/5 deletion led to deregulation of lipoprotein pathways, loss of BA secretion, intrinsic alterations of lipid homeostasis and the onset of NAFLD. Lay summaryThe Wnt/{beta}-catenin pathway plays an important role during development and tissue homeostasis. Loss of Wnt/{beta}-catenin activity in mouse liver leads to loss of liver zonation, but the impact on nonalcoholic fatty liver disease (NAFLD) remains unclear. We show that livers of mice developed steatosis upon deletion of the positive pathway regulators Lgr4/5. Livers of knock-out (KO) mice exhibited altered lipid composition due to impaired lipid secretion. Furthermore, livers of these mice developed a nonalcoholic steatohepatitis (NASH)-like phenotype and fibrotic features derived from activated hepatic stellate cells. Our data demonstrate a protective role of Wnt/{beta}-catenin pathway activity towards the development of NAFLD. HighlightsO_LIAbrogation of hepatic Wnt/{beta}-catenin activity and liver zonation upon Lgr4/5 deletion in mice led to hepatic steatosis. C_LIO_LILiver fat accumulation was caused by impaired lipid secretion from hepatocytes. C_LIO_LISteatotic livers contained increased levels of diverse lipid species, including polyunsaturated fatty acids and triglycerol-estolides. C_LIO_LIThese data confirmed that a decrease in Wnt/{beta}-catenin signaling led to the development of nonalcoholic fatty liver disease (NAFLD) in mice. C_LI

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Saponara, E., Penno, C., Matadamas Guzman, M. L., Brun, V., Fischer, B., Brousseau, M., Wang, Z.-Y., ODonnell, P., Turner, J., Graff Meyer, A., Bollepalli, L., dArio, G., Roma, G., Carbone, W., Orsini, V., Annunziato, S., Obrecht, M., Beckmann, N., Saravanan, C., Osmont, A., Tropberger, P., Richards, S., Genoud, C., Aebi, A., Ley, S., Ksiazek, I., Nigsch, F., Terraciano, L., Bouwmeester, T., Tchorz, J., Ruffner, H.. 2021-11-22. Loss of hepatic Lgr4 and Lgr5 promotes nonalcoholic fatty liver disease. https://doi.org/10.1101/2021.11.22.469602

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