TRIIODOTHYRONINE (T3) TRIGGERS A METABOLIC REPROGRAMMING ON MICE DENDRITIC CELLS (DC)

BLANCO ANTONELLA; NEGRETTI- BORGA DANA MARÍA; PUENTES ELIDA NAHIR; PIRES TEIXEIRA MARIANA ; DONADIO ANA CAROLINA; MONTESINOS MARÍA DEL MAR; PELLIZAS CLAUDIA GABRIELA

Mar del Plata

Congreso; REUNIÓN CONJUNTA SAIC SAI&FAIC SAFIS 2022; 2022

Sociedad Argentina de Investigación Clíncia, Sociedad Argentina de Inmunología, Sociedad Argentina de Fisiología

Our group previously demonstrated that T3 triggers adaptive pro-inflammatory and cytotoxic responses through DC activation, restraining regulatory signals. These results were successfully exploited in T3-stimulated DC (T3-DC)-based antitumor vaccines against melanoma and colon carcinoma in mice. It is known that metabolic reprogramming of DC supports its TLR-driven maturation, favoring glycolysis over oxidative phosphorylation (OXPHOS), and is controlled by different time-dependent pathways. Sustained commitment to glycolysis relays on OXPHOS inhibition caused by nitric oxide (NO) produced by inducible NO Synthase (iNOS). On this basis, and given the potential of T3-DC vaccines, our aim was to assess T3 effects on DC’s metabolic programming. Immature bone marrow derived DC (iDC) were obtained from C57BL/6 mice and stimulated (or not) with T3 (10nM) for different time points. Glucose and lactate were measured in culture’s supernatants (SN) from iDC and T3-DC with commercial kits. Glucose uptake was evaluated using the glucose analog fluorescent dye 2-NBDG by FACS. Glucose transporter 1 (Glut-1) and iNOS expression were analyzed by Western Blot. Nitrite levels in SN were measured by the Griess reaction. Statistical analysis: t test or t test with Welch’s correction, p