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Estep, J. A.

Publications and source records attributed to Estep, J. A..

3 recordsLinked to original sources

Functional Role for Cas Cytoplasmic Adaptor Proteins During Cortical Axon Pathfinding

Proper neural circuit organization requires individual neurons to project to their targets with high specificity. While several guidance molecules have been shown to mediate axonal fasciculation and pathfinding, less is understood about how neurons intracellularly interpret and integrate these cues. Here we provide genetic evidence that the Crk-Associated Substrate (Cas) family of intracellular adaptor proteins is required for proper fasciculation and guidance of two cortical white matter tracts: the Anterior Commissure (AC) and thalamocortical axons (TCAs). Using a Cas Triple Conditional Knock Out (Cas TcKO) mouse model, we show that Cas proteins are required for proper TCA projection by a non-neuronal cortical cell population. We also demonstrate a requirement of the {beta}1-integrin receptor for TCA projection, similarly in a population of non-neuronal cortical cells. Additional analysis of Cas TcKO mutants reveals a role for Cas proteins in AC fasciculation, here within the neurons themselves. This AC fasciculation requirement is not phenocopied in {beta}1-integrin deficient mutants, suggesting that Cas proteins might signal downstream of a different receptor during this axon pathfinding event. These findings implicate Cas proteins as key mediators of cortical axon tract fasciculation and guidance. Author SummaryIn the developing nervous system, neurons extend axons--long projections that relay information to their targets--to establish neural circuits. Axons follow specific pathways directed by extracellular guidance cues, much like street signs direct traffic. While these guidance cues are well studied, how neurons internally interpret and respond to these signals remains unclear. Here, we examine the role of the Crk-Associated Substrate (Cas) family of intracellular adaptor proteins in axon guidance within cortical axon tracts. Using genetic techniques to selectively remove Cas gene function from specific cell types, we demonstrate that Cas proteins are required for proper fasciculation (bundling) of anterior commissure axons, acting directly within the projecting axons themselves. Additionally, Cas proteins are required for proper guidance of thalamocortical projections--axons connecting the thalamus with the cortex. However, in this case, Cas proteins do not act within projecting axons but instead direct target neurons to their final positions. We further show that the {beta}1-integrin receptor is similarly required for thalamocortical axon projection. These findings provide genetic evidence for a critical role of Cas adaptor proteins in both fasciculation and guidance of cortical axon tracts.

neuroscience↗

An adhesive signaling axis regulates the establishment of the cortical glial scaffold.

The mature mammalian cortex is composed of six architecturally and functionally distinct layers. Two key steps in the assembly of this layered structure are the initial establishment of the glial scaffold and the subsequent migration of post-mitotic neurons to their final position. These processes involve the precise and timely regulation of adhesion and detachment of neural cells from their substrates. Although much is known about the roles of adhesive substrates during neuronal migration and the formation of the glial scaffold, less is understood about how these signals are interpreted and integrated within these neural cells. Here, we provide in vivo evidence that Cas proteins, a family of cytoplasmic adaptors, serve a functional and redundant role during cortical lamination. Cas triple conditional knock-out (Cas TcKO) mice display severe cortical phenotypes that feature cobblestone malformations. Molecular epistasis and genetic experiments suggest that Cas proteins act downstream of transmembrane Dystroglycan and {beta}1-Integrin in a radial glial cell-autonomous manner. Overall, these data establish a new and essential role for Cas adaptor proteins during the formation of cortical circuits and reveal a signaling axis controlling cortical scaffold formation.

neuroscience↗

The RacGAP βChimaerin is essential for cerebellar granule cell migration

During mammalian cerebellar development, postnatal granule cell progenitors proliferate in the outer part of the External Granule Layer (EGL). Postmitotic granule progenitors migrate tangentially in the inner EGL before switching to migrate radially inward, past the Purkinje cell layer, to achieve their final position in the mature Granule Cell Layer (GCL). Here, we show that the RacGAP {beta}-chimaerin is expressed by a small population of late-born, premigratory granule cells. {beta}-chimaerin deficiency causes a subset of granule cells to become arrested in the EGL, where they differentiate and form ectopic neuronal clusters. These clusters of granule cells are able to recruit aberrantly projecting mossy fibers. Collectively, these data suggest a role for {beta}-chimaerin as an intracellular mediator of Cerebellar Granule Cell radial migration.

neuroscience↗