Evento
Neural stem cells-derived neurons obtained from human pluripotent stem cells as an in vitro model for studying CDK5/p25 mediated neurodegenerative processes
Mucci, Sofia; Rodríguez Varela, Maria Soledad
; Isaja, Luciana
; Sevlever, Gustavo Emilio; Scassa, Maria Elida; Romorini, Leonardo



Tipo del evento:
Reunión
Nombre del evento:
LXIII Reunión Anual de la de la Sociedad Argentina de Investigación Clínica; LXVI Reunión Anual de la Sociedad; Reunión Anual de la Sociedad Argentina de Fisiología
Fecha del evento:
14/11/2018
Institución Organizadora:
Sociedad Argentina de Investigación Clínica;
Sociedad Argentina de Inmunología;
Sociedad Argentina de Fisiología;
Sociedad Argentina de Virología;
Asociación Argentina de Naomedicinas;
Título de la revista:
Medicina (Buenos Aires)
Editorial:
Fundación Revista Medicina
ISSN:
1669-9106
Idioma:
Inglés
Clasificación temática:
Resumen
Human embryonic and induced pluripotent stem cells (hESCs and IPSCs)can differentiate into a wide range of specialized cells,including neural stem cells (NSC). Moreover, NSC-derived neurons are proposed as a model for studying neurodegeneration. CDK5/ p35 complex is involved in neuronal homeostasis and development. However, its functionis deregulated in neurodegeneration by p35 cleavage in p25, which allows the aberrant phosphorylation of targets through the constitution of a more stable complex CDK5/p25. In this work we aimed to set up an in vitroCDK5/p25 neurodegenerative model using NSC-derived neurons obtained from hESCs and hIPSCs subjected to different cellular stressors. For this purpose, we first derived NSC from hESC (H9 line) and hIPSC (FN 2.1 line), which were further differentiated into neuronsusin a neural induction kit. NSC and neuron-like phenotype were validated by immunofluoresce and RT-qPCR of cell specific markers (sox-1, Sox-2, pax-6 and nestin for NSC; MAP5, MAP2 and Tuj-1 for neurons). Then, CDK5 and p35 mRNA and protein expression levels were analyzed in hESCs, hIPSCs, NSC and neurons by RT-qPCR and western blot. Interestingly, we observed that althought CDK5 was ubiquitous, p35 mRNA and protein were mainly expressed in neurons. We next evaluated how different stress stimuli (rotenone, glutamate and calcium ionophore A23187) affected NSC andneurons viability. We determined the percentage of cell viability after 24 hours treatment with increasing concentrations of rotenone and glutamate and 2 hours treatment with A23187 using an XTT vital dye assay. Cell viability felt downsignificantly in the case of rotenone and A23187 treatments in a concetration dependent manner. In conclusion, NSC-derived neurons obtained from hESCs andhiPSCs expressed high levels of p35 and responded to rotenone stressor, making them a suitable CDK5/p25 neurodegenerative invitro model.
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Identificadores
Colecciones
Eventos (INEU)
Eventos de INSTITUTO DE NEUROCIENCIAS
Eventos de INSTITUTO DE NEUROCIENCIAS
Eventos(SEDE CENTRAL)
Eventos de SEDE CENTRAL
Eventos de SEDE CENTRAL
Citación
Neural stem cells-derived neurons obtained from human pluripotent stem cells as an in vitro model for studying CDK5/p25 mediated neurodegenerative processes; LXIII Reunión Anual de la de la Sociedad Argentina de Investigación Clínica; LXVI Reunión Anual de la Sociedad; Reunión Anual de la Sociedad Argentina de Fisiología; Mar del Plata; Argentina; 2018; 158-158
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