3A and

Supporting Fig. 4E). Third, we found that TGR5 KO mice were significantly more sensitive to extrahepatic cholestasis induced by BDL, because they exhibited larger and more numerous necrotic areas on H&E-stained liver sections, higher ALT, bilirubin, and ALP elevations in plasma, and increased BA overload, as compared to WT mice (Fig. 3B,C and Supporting Fig. 4F). Finally, we found that TGR5 KO mice fed with a 1% cholic acid (CA)-enriched diet exhibited an increase in plasma ALT, ALP, and bilirubin (Supporting Fig. 4G), hepatic BA overload, parenchymal neutrophil infiltration, hepatic necrosis, and elevated tumor necrosis factor alpha (TNF-α) mRNA, whereas WT mice did not[21] (Fig. 3D,E). In agreement with

the inhibitory effect of TGR5 on cytokine gene induction and production in macrophages and KCs,[10, 12, 14] we found that plasma rise in interleukin (IL)−6, TNF-α www.selleckchem.com/products/Y-27632.html and IL-1β concentrations 4 hours after PH was significantly higher in TGR5 KO than in WT mice (Fig. 4A). Hepatic infiltration by neutrophils was also strikingly more intense in TGR5 KO than WT mice after PH or BDL (Fig. 4B). Interestingly, KC depletion with clodronate liposomes, significantly reducing the post-PH induction of cytokine gene, also reduced the occurrence of hepatic necrosis Talazoparib 72 hours after PH (Fig. 4C). Altogether, these data suggest that TGR5 is mandatory for liver protection against BA toxicity and excessive cytokine production, as revealed in different experimental settings of BA overload (PH, BDL, and 1% CA-enriched diet) and BA sequestration (CT diet). Based on these

data, we investigated whether TGR5 may contribute to adapt bile flow in circumstances of BA overload after PH or BDL. Interestingly, ever biliary BA composition was more hydrophobic in TGR5 KO than in WT mice, as calculated on the basis of mass spectrometry analysis,[22] both before and after PH (Fig. 5A). This more hydrophobic BA composition in TGR5 KO mice was also found in plasma and liver before and after PH (Fig. 5B,C) as well as in feces (Supporting Fig. 5A). Namely, muricholic acid (MCA), a hydrophilic primary BA in mice, whose relative concentration is maintained or increased during cholestasis,[21] as well as the MCA/CA ratio taken as a marker of hydrophobicity, were strongly reduced in TGR5 KO mice before and after PH, as compared to WT mice (Fig. 5B,C and Supporting Fig. 5A). Of note, cytochrome P450 (7a1, 8b1, 27a1, 3A11, and 2b10) and sulfotransferase 2a mRNA expressions were similar in WT and TGR5 KO mice (Supporting Fig. 5B). Basal bile flow was slightly smaller in TGR5 KO than in WT mice, as previously reported[17]; however, 48 hours after PH, bile flow increased significantly in WT, as previously described,[5] but not in TGR5 KO mice (Fig. 6A).