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. 2012 Jul 31;303(7):E908–E916. doi: 10.1152/ajpendo.00663.2011

Fig. 1.

Fig. 1.

L6-GLUT4myc cells were stably transfected with either an empty lentiviral vector or a tribbles 3 (TRIB3) short-hairpin RNA (shRNA) lentiviral vector. A: knockdown (KD) of TRIB3 protein in L6 muscle cells. B: basal (open bars) and insulin-stimulated (filled bars) glucose uptake rates were measured; values are means ± SD. C–E: L6 cells were stably transfected with either an empty lentiviral vector or a TRIB3 shRNA lentiviral vector and analyzed by Western blot for phosphorylated insulin receptor substrate-1 (p-IRS-1) at the Tyr612 site (C), p-Akt at the Ser473 site (D), and p-ERK (E) with or without 45 min of 100 nM insulin stimulation. *P < 0.05. Values are means ± SD for 3 repeated experiments.