IBIOBA - MPSP   22718
INSTITUTO DE INVESTIGACION EN BIOMEDICINA DE BUENOS AIRES - INSTITUTO PARTNER DE LA SOCIEDAD MAX PLANCK
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
IL-6 INTRACELLULAR SIGNALING IN NATURAL AND INDUCED SENESCENT CELLS
Autor/es:
SAPOCHNIK, M; ELGUERO, B; THEODOROPOULOU, M.; ATTORRESI, A; FUERTES, M; PONTEL, L; HERBSTEIN, F; SENIN, S; MÜLLER, L; ARZT, E
Lugar:
Virtual
Reunión:
Congreso; REUNIÓN DE SOCIEDADES DE BIOCIENCIAS 2021; 2021
Institución organizadora:
Sociedad Argentina de Investigación Clínica
Resumen:
Senescence is defined as a growth arrest program that preserves physiological cell functions. It has been associated with tumor suppressor mechanisms as well as a resistance mechanism to evade tumor eradication. Interleukin-6 (IL-6) is part of the secretome of senescent cells denominated senescence associated secretory phenotype (SASP). In previous work we demonstrated the relevance of the intracellular IL-6 signaling in vitro and in vivo in a model of senescent pituitary tumor cells. In this work we focus on the characterization of this signaling in a natural and therapy-induced senescent model. In MtT/S cells, a naturally senescent pituitary somatotroph cell line, to discriminate the effect of intracellular action of IL-6 we inhibited secretory pathway using two independent approaches: a) overexpression of a dominant negative form of Rab11 which is a key molecule in anterograde transport, involved in IL-6 associated vesicle exocytosis and b) treatment with brefeldin A (BFA) 100 ng/ml, a drug that blocks intracellular vesicle transport from endoplasmic reticulum to Golgi.In both cases we observed an increase in the senescent biomarkers pRb and p16INK4 (measured by western blot) and the activity of senescence associated β galactosidase (SA-β-Gal) (n=4, p