Haynie, Christopher; Freitas, Claudia M. Tellez; Whitley, Kiara V.; Weber, K. Scott (Brigham Young University)
Faculty Advisor: Weber, K. Scott (Life Sciences, Microbiology and Molecular Biology)
T cells play a critical role in the adaptive immune response and undergo significant metabolic changes upon activation. T cell co-receptors influence T cell activation and function, yet their influence on T cell metabolism remains unclear. CD5, an inhibitory co-receptor expressed on the surface of T cells, is known to regulate thymocyte selection and T cell receptor (TCR) signaling. We previously observed that CD5 plays a critical role in calcium signaling in naïve helper T cells. As calcium signaling influences metabolic changes in cells, our current work focuses on understanding the role of CD5 in T cell metabolism. To understand how CD5 regulates metabolism in T cells, we used CD5 deficient T cells and compared them to wildtype CD5 sufficient T cells. We have characterized their metabolic activity using glycolytic and mitochondrial respiration assays. Interestingly, CD5 deficient naïve T cells have increased glycolysis, mitochondrial respiration, and spare respiratory capacity in comparison to wildtype T cells. We hypothesize that this is due to CD5 altering mitochondrial membrane potential and mass, gene regulation, and the influence of different cellular fuels. Understanding how CD5 regulates T cell metabolism will provide critical insights for improved immunotherapeutic strategies.