Glucose withdrawal induces supra‐physiological levels of tyrosine phosphorylation in cells sensitive to glucose withdrawal. Glucose withdrawal induces.

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Glucose withdrawal induces supra‐physiological levels of tyrosine phosphorylation in cells sensitive to glucose withdrawal. Glucose withdrawal induces supra‐physiological levels of tyrosine phosphorylation in cells sensitive to glucose withdrawal. (A) LN18, LN229, T98, and U87 GBM cell lines were starved of glucose and pyruvate for 24 h. Trypan blue exclusion measurements demonstrated that LN18, T98, and U87, but not LN229, show a rapid and complete loss of viability following glucose withdrawal. (B) Western blotting with a phospho‐tyrosine antibody revealed that the glucose withdrawal‐sensitive cell lines (LN18, T98, and U87) exhibit a dramatic induction of phospho‐tyrosine signaling at the indicated times following glucose withdrawal. Conversely, the glucose withdrawal‐insensitive cell line LN229 showed no increase in phospho‐tyrosine levels following glucose withdrawal. Actin served as an equal loading control. (C–E) Glucose withdrawal induces supra‐physiological levels of phospho‐tyrosine signaling even in cells expressing a constitutively active tyrosine kinase. (C) Expression of the constitutively active EGFR mutant EGFRvIII in U87 cells induces high levels of phospho‐tyrosine signaling as demonstrated by western blotting with an anti‐phospho‐tyrosine antibody. (D) Expression of the constitutively active EGFRvIII mutant in U87 cells (U87‐EGFRvIII) does not alter the sensitivity to glucose withdrawal at 24 h. Error bars are standard deviation of the mean. (E) U87‐EGFRvIII cells demonstrate a rapid induction of phospho‐tyrosine signaling at the times indicated following glucose withdrawal. For phospho‐tyrosine, both dark and light film exposures are shown. (F–I) Human sarcoma‐ and melanoma‐derived cell lines also demonstrate a correlation between sensitivity to glucose withdrawal and rapid induction of supra‐physiological phospho‐tyrosine levels. (F) The sarcoma cell lines HT161 and TC32 were starved of glucose and pyruvate and their viability was measured by Trypan blue exclusion at the indicated times. TC32 cells show a rapid and complete loss of viability, whereas HT161 were relatively insensitive to glucose withdrawal. Error bars are standard deviation of the mean. (G) Western blotting with an anti‐phospho‐tyrosine antibody demonstrated that TC32, but not HT161, show induction of hyper‐phosphorylation after 2 h of glucose starvation. (H) Melanoma cell lines M202, M207, M229, and M249 were starved of glucose and pyruvate for 24 h. Trypan blue exclusion measurements revealed that M202 and M207, but not M229 or M249 cells, showed significant loss of cell viability after 24 h of glucose withdrawal. Error bars are standard deviation of the mean. (I) Western blotting demonstrated that 7 h of glucose withdrawal induced supra‐physiological tyrosine phosphorylation in M202 and M207, but not M229 or M249. Nicholas A Graham et al. Mol Syst Biol 2012;8:589 © as stated in the article, figure or figure legend