Adjuvant Induced Glucose Uptake by Activated T Cells is not Correlated with Increased Survival

  • Sadhak Sengupta
  • Rebecca J. Vitale
  • Paula M. Chilton
  • Thomas C. Mitchell
Part of the Advances In Experimental Medicine And Biology book series (AEMB, volume 614)


Authors contributed equally to this manuscript Natural adjuvants, such as bacterial lipopolysaccharide (LPS), activate antigen presenting cells via Toll-like receptors and, indirectly, increase the survival of antigenactivated T cells. The molecular mechanisms leading to increased survival remain poorly defined. Because T cell clonal expansion leads to high energy demands, we hypothesized that increased glucose uptake and/or utilization in adjuvant-activated T cells could be important molecular event(s) that would lead to adjuvant-associated T cell survival advantage. Using a fluorescent analog of 2-deoxyglucose, 2-NBDG, we measured glucose accumulation and rate of uptake in T cells from mice treated with antigen in the absence or presence of LPS. Although adjuvant activated T cells increased the accumulation of 2-NBDG, the rate of uptake was unchanged compared to cells activated with only antigen. Furthermore, glucose transport inhibitors, cytochalasin B or phloretin, decreased the accumulation of glucose in adjuvant- treated T cells, but this decrease did not impair adjuvant-associated survival advantages. Together, these data indicate that increased glucose uptake through glucose transporters is not required for increased survival of activated T cells.


Glucose Uptake Increase Glucose Uptake Glucose Accumulation Fluorescent Analog Inhibit Glucose Uptake 
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© Springer Science+Business Media, LLC 2008

Authors and Affiliations

  • Sadhak Sengupta
  • Rebecca J. Vitale
  • Paula M. Chilton
    • 1
  • Thomas C. Mitchell
    • 1
  1. 1.Institute for Cellular Therapeutics, University of Louisville School of MedicineLouisville

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