“
“The corpus callosum Dinaciclib clinical trial coordinates interhemispheric functions critical for cognition by providing axonal connectivity across the midline between cortical areas that are required for a variety of sensory, motor, and emotional processing. In addition, callosal agenesis is associated with a wide variety of neurodevelopmental and psychiatric diseases (Paul et al., 2007). The corpus

callosum develops late in gestation and is evolutionarily young, having developed in importance as neocortical size and function increased (Mihrshahi, 2006). In mice, medially projecting callosal axons reach the midline at embryonic day 15 (E15), and the first cingulate pioneer axons cross the midline at E16 (Koester and O’Leary, 1994, Ozaki and Wahlsten, 1998 and Rash and Richards, 2001). If cortical axons approach the midline but the pathfinding

cells do not cross the midline, the callosum fails to form and Probst bundles form, which consist of cortical axons projecting anterior-posterior instead of crossing the midline (Paul et al., 2007). The paired cerebral hemispheres develop by producing excitatory projection neurons in the neurogenic niche adjacent to the ventricles. These cells migrate radially away from the ventricles to generate laminae in the more superficial cortex. Maturation of the cortical neurons occurs near the meningeal Amine dehydrogenase surface, and many neurons send dendrites toward the pial surface, whereas axons generally project in the opposite direction toward the ventricle, eventually turning C59 wnt molecular weight laterally to project caudally out of the cortex or medially to project across the callosum. The midline meninges, across which the callosum forms, is the only site in the cortex where axons reach and project across the pial surface. The three cortical meningeal layers are derived from the cranial neural crest,

which generates a variety of cellular derivatives important for face and head development and evolution (Serbedzija et al., 1992). Recently, we reported that the meninges are a key regulator of embryonic cortical neurogenesis by secreting an instructive cue (retinoic acid) that regulates the onset of neuron production (Siegenthaler et al., 2009). These data, along with previous work from our laboratory and others (Borrell and Marín, 2006, Li et al., 2008, Li et al., 2009, López-Bendito et al., 2008 and Paredes et al., 2006), indicate that the meninges are an instructive signaling source during cortical development. This led us to consider the idea that the meninges may also play a role in axon guidance during callosum formation, because these axons appear to directly interact with the meninges (Alcolado et al., 1988). There are still major unanswered questions about how the corpus callosum forms.