Suppression of oxidative metabolism and mitochondrial biogenesis by the transcriptional corepressor RIP140 in mouse adipocytes
J. Clin. Invest. Aimee M. Powelka, et al. 116:125 doi:10.1172/JCI26040 [
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Figure 7RIP140 depletion enhances glycolysis and TCA cycling, but not triglyceride synthesis or de novo free fatty acid synthesis. Eight days after the induction of differentiation, 3T3-L1 adipocytes were transfected with scrambled or RIP140 siRNA. After 72 hours, cells were starved and glucose metabolism (with continued starvation [basal] or 1 μM insulin stimulation) was measured by [6-
14C]-glucose conversion into carbon dioxide (CO
2), triglycerides, and fatty acids as described in Methods. Graphs show the mean ± SEM of 3–4 independent experiments. *
P < 0.05 compared with scrambled, by Student’s
t test.