c-Fos importance for brain development

an immediate early response gene involved in cell proliferation and differentiation after extracellular stimuli, whereas its deregulation has been associated to oncogenic progression. As other members of the FOS family proteins (Fra-1, Fra-2, FosB) and proteins of the ATF family, c-Fos can heterodimerize with members of the JUN family (c-Jun, JunB, JunD) to form the transcription factor activator protein 1 (AP-1). As an AP-1 heterodimer, c-Fos is considered a master switch that transduces short-term stimuli into long-term responses. Independently of its AP-1 activity, c-Fos is also an activator of phospholipid synthesis at the cytoplasmic level in events demanding high rates of membrane biogenesis, as occurs for example in the exacerbated growth of tumor cells [1]. Only ~40% of c-fos-/-mouse embryos survive until birth showing the importance of c-Fos for development. Moreover, surviving animals live to an average age of 6-7 months, show growth retardation, severe osteopetrosis, delayed or absent gametogenesis and altered haematopoiesis. Decrease of c-fos expression leading to modifications in the composition of AP-1 factors (particularly increasing the Jun/Jun homodimers) has been associated with cellular replicative senescence [2], suggesting a possible involvement of cell senescence in premature death of c-fos-/-mice. c-Fos is currently used as a marker of neuronal activity and has been associated with a number of neural and behavioral responses to acute stimuli expression. In fact, age-related changes in neuronal function and plasticity with a concomitant decrease in the level of c-Fos have been observed in different brain regions [3]. In addition to the above-mentioned alterations, the c-fos-/-mice show behavioral alterations such as learning impairment, hyperactivity and abnormal sexual behavior. In spite of all these evidences that show a relationship between c-Fos expression and neuronal function, its role in brain development has been poorly investigated. We have recently reported that c-Fos plays an important and unsuspected role in neurogenesis [4]. Adult c-fos-/-mice present a ̴ 40-60% reduction in their body weight and their brain size is significantly smaller as compared to c-fos +/+ mice. We have shown that this correlates with a decreased brain cell number. We have thus examined the importance of c-Fos for neo-Editorial cortex development by comparing these two types of mice at different embryonic stages. c-fos-/-embryos present a ~15% reduction in the thickness of the developing cortex as compared to wt controls. Immuno-staining revealed that this was related to a decrease in neurogenesis in c-fos-/-mice during embryonic development. Indeed we showed both a …