Artículos de revistas
Brain development is impaired in c-fos -/- mice
Fecha
2015-07Registro en:
Velazquez, Fabiola Noelia; Prucca, Cesar German; Etienne, Olivier; D'Astolfo, Diego S.; Silvestre, David C.; et al.; Brain development is impaired in c-fos -/- mice; Impact Journals LLC; Oncotarget; 6; 19; 7-2015; 16883-16901
1949-2553
CONICET Digital
CONICET
Autor
Velazquez, Fabiola Noelia
Prucca, Cesar German
Etienne, Olivier
D'Astolfo, Diego S.
Silvestre, David C.
Boussin, Francois D.
Caputto, Beatriz Leonor
Resumen
c-Fos is a proto-oncogene involved in diverse cellular functions. Its deregulation has been associated to abnormal development and oncogenic progression. c-fos-/- mice are viable but present a reduction in their body weight and brain size. We examined the importance of c-Fos during neocortex development at 13.5, 14.5 and 16.5 days of gestation. At E14.5, neocortex thickness, apoptosis, mitosis and expression of markers along the different stages of Neural Stem Progenitor Cells (NSPCs) differentiation in c-fos-/- and wild-type mice were analyzed. A ~15% reduction in the neocortex thickness of c-fos-/- embryos was observed which correlates with a decrease in the number of differentiated cells and an increase in apoptosis at the ventricular zone. No difference in mitosis rate was observed, although the mitotic angle was predominantly vertical in c-fos-/- embryos, suggesting a reduced trend of NSPCs to differentiate. At E13.5, changes in differentiation markers start to be apparent and are still clearly observed at E16.5. A tendency of more AP-1/DNA complexes present in nuclear extracts of cerebral cortex from c-fos-/- embryos with no differences in the lipid synthesis activity was found. These results suggest that c-Fos is involved in the normal development of NSPCs by means of its AP-1 activity.