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. 2014 Nov 3;124(12):5424–5436. doi: 10.1172/JCI76289

Figure 3. LysM-Cre Tgr5fl/fl mice display impaired insulin responsiveness.

Figure 3

(A) Body weight curves of Tgr5fl/fl and LysM-Cre Tgr5fl/fl mice fed HFD for 12 weeks. n = 12 per group. (B) Body composition (fat and lean mass) of Tgr5fl/fl and LysM-Cre Tgr5fl/fl mice, determined by EchoMRI. n = 12 per group. (C) Left: Blood glucose levels during ITT (insulin; 0.75 U/kg) in Tgr5fl/fl and LysM-Cre Tgr5fl/fl mice fed HFD for 10 weeks. Right: Average AUC. n = 12 per group. (D) Left: Plasma insulin levels during OGTT in Tgr5fl/fl and LysM-Cre Tgr5fl/fl mice fed HFD for 8 weeks. Right: Average AUC. n = 12 per group. (E) Left: Blood glucose levels during OGTT in Tgr5fl/fl and LysM-Cre Tgr5fl/fl mice fed HFD. Right: AUC. n = 12 per group. (F) HOMA-IR of HFD-fed Tgr5fl/fl and LysM-Cre Tgr5fl/fl mice. n = 12 per group. (GI) Western blot of phospho-AKT (Ser473), total AKT, and HSP90 in (G) liver, (H) gastrocnemius muscle, and (I) eWAT of HFD-fed Tgr5fl/fl and LysM-Cre Tgr5fl/fl mice injected i.p. with vehicle or insulin (1 U/kg; 10 min). Quantitative densitometry of Western blots is also shown. n = 6 per group. Results represent mean ± SEM. *P < 0.05, **P < 0.01 vs. genotype; #P < 0.001 vs. control, 2-tailed Student’s t test or 1- or 2-way ANOVA with Bonferroni post-hoc analysis as appropriate.