Abstract

Precise wiring of cortical circuits during development depends upon axon extension, guidance, and branching to appropriate targets. Motile growth cones at axon tips navigate through the nervous system by responding to molecular cues, which modulate signaling pathways within axonal growth cones. Intracellular calcium signaling has emerged as a major transducer of guidance cues but exactly how calcium signaling pathways modify the actin and microtubule cytoskeleton to evoke growth cone behaviors and axon branching is still mysterious. Axons must often pause their extension in tracts while their branches extend into targets. Some evidence suggests a competition between growth of axons and branches but the mechanisms are poorly understood. Since it is difficult to study growing axons deep within the mammalian brain, much of what we know about signaling pathways and cytoskeletal dynamics of growth cones comes from tissue culture studies, in many cases, of non-mammalian species. Consequently it is not well understood how guidance cues relevant to mammalian neural development in vivo signal to the growth cone cytoskeleton during axon outgrowth and guidance. In this review we describe our recent work in dissociated cultures of developing rodent sensorimotor cortex in the context of the current literature on molecular guidance cues, calcium signaling pathways, and cytoskeletal dynamics that regulate growth cone behaviors. A major challenge is to relate findings in tissue culture to mechanisms of cortical development in vivo. Toward this goal, we describe our recent work in cortical slices, which preserve the complex cellular and molecular environment of the mammalian brain but allow direct visualization of growth cone behaviors and calcium signaling. Findings from this work suggest that mechanisms regulating axon growth and guidance in dissociated culture neurons also underlie development of cortical connectivity in vivo.

Highlights

  • The development of appropriate connections is essential for the nervous system to function correctly

  • In collateral branches semaphorin 3A caused collapse of splayed microtubules and disappearance of actin bundles leading to a decrease in cortical axon branching. These results demonstrate that axon outgrowth and branching may in some cases be differentially regulated since netrin-1 and semaphorin 3A increased or decreased cortical axon branching respectively without affecting axon length

  • mitogen activated protein kinases (MAPKs) over expression increased axon branching whereas MAPK inhibition prevented netrin-1 induced branching but did not affect axon length. These results demonstrate for the first time that the axon guidance cue netrin-1 evokes rapid cortical axon branching through repetitive Ca2+ transients that activate the downstream kinases calmodulin-dependent protein kinase II (CaMKII) and MAPK, which are sensitive to changes in the frequency of Ca2+ transients

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Summary

Introduction

The development of appropriate connections is essential for the nervous system to function correctly. We identified guidance cues that promote cortical axon outgrowth, guidance, and branching, the intracellular calcium signaling pathways that evoke these axonal responses and the cytoskeletal mechanisms that regulate them.

Results
Conclusion
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