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. 2019 Feb 4;9:1350. doi: 10.1038/s41598-018-38014-3

Figure 3.

Figure 3

ApoA-I increases insulin-dependent glucose uptake in HSKMCS in an IRS-1 and PI3K/Akt/AS160-dependent manner. (A) HSKMCs were transfected with scrambled siRNA (scr siRNA) or IRS-1 siRNA. IRS-1 protein expression was quantified by immunoblotting. (B) Scr-siRNA- (open bars) and IRS-1 siRNA-transfected (closed bars) HSKMCs were pre-incubated with or without apoA-I then incubated in the presence or absence of insulin. Glucose uptake was quantified as described in the legend to Fig. 1. (C–E) Total and phosphorylated Akt, and AS160 were determined by immunoblotting after incubation in the presence (closed bars) and absence (open bars) of wortmannin. (F) Glucose uptake in HSKMCs was determined in the presence (closed bars) and absence (open bars) of wortmannin as described in Materials and Methods. All values represent the mean ± SD of three independent experiments. Glucose uptake was normalized to 1 nmol/mg/h for control scr siRNA-transfected cells. ***p < 0.001 vs. control for scr siRNA-transfected cells or cells incubated in the absence of wortmannin; p < 0.05 versus control IRS-1 siRNA-transfected cells; †††p < 0.001 versus cells incubated with wortmannin under control conditions.