UCP2 Invalidation Increases HK2 Protein Expression and Decreases LDHA and G6PDH Activities in Colon Tumors
(A) Mitochondrial respiration rate was determined in the presence of 10 mM pyruvate, 5 mM malate, and 1.4 mM ADP. The leak was measured after adding 1 μg/mL oligomycin (Ucp2+/+ T n = 10, Ucp2−/− T n = 9).
(B) CS enzyme activity normalized to protein content. Data represent means ± SEMs (Ucp2+/+ T n = 11, Ucp2−/− T n = 7).
(C) Scheme showing the 14CO2-producing reactions from [U-14C]-glucose (red) and [2-14C]-pyruvate (blue).
(D) [U-14C]-glucose (Ucp2+/+ n = 11, Ucp2−/− n = 12) and [2-14C]-pyruvate (Ucp2+/+ n = 7, Ucp2−/− T n = 9) oxidation into 14CO2 of Ucp2+/+and Ucp2−/− colon tumors (T). Data indicate means ± SEMs.
(E) Immunoblots and quantifications of HK2 and LDHA expression using whole-cell extracts from colon tumors. Data indicate means ± SEMs (n = 8–12).
(F) LDH enzyme activity. Data represent means ± SEMs (Ucp2+/+ n = 5, Ucp2−/− n = 6).
(G) G6PDH enzyme activity relative to Ucp2+/+ T (Ucp2+/+ n = 7, Ucp2−/− n = 8).
See also Figures S3 and S4.