AI Article Synopsis

  • Neurons use axons to reach their targets, influenced by attractive or repulsive cues, but the decision-making process of growth cones when encountering repulsive signals is not fully understood.
  • Researchers created a microcontact printing culture system to isolate axonal tips in a permissive area surrounded by the repulsive signal semaphorin 3F, which affected axon growth rates and patterns.
  • The study found that axonal tips could "jump" over repulsive signals to grow straight, influenced by the spacing of the permissive dots and intracellular signaling, suggesting the system could be useful for studying factors affecting axonal growth.

Article Abstract

Neurons reach their correct targets by directional outgrowth of axons, which is mediated by attractive or repulsive cues. Growing axons occasionally cross a field of repulsive cues and stop at intermediate targets on the journey to their final destination. However, it is not well-understood how individual growth cones make decisions, and pass through repulsive territory to reach their permissive target regions. We developed a microcontact printing culture system that could trap individual axonal tips in a permissive dot area surrounded by the repulsive signal, semaphorin 3F (Sema3F). Axons of rat hippocampal neurons on the Sema3F/PLL dot array extended in the checkboard pattern with a significantly slow growth rate. The detailed analysis of the behaviors of axonal growth cones revealed the saccadic dynamics in the dot array system. The trapped axonal tips in the permissive area underwent growth cone enlargement with remarkably spiky filopodia, promoting their escape from the Sema3F constraints with straight extension of axons. This structured axonal growth on the dot pattern was disrupted by increased inter-dot distance, or perturbing intracellular signaling machineries. These data indicate that axons grow against repulsive signals by jumping over the repulsive cues, depending on contact signals and intracellular milieu. Our study suggests that our dot array culture system can be used as a screening system to easily and efficiently evaluate ECM or small molecule inhibitors interfering growth cone dynamics leading to controlling axonal growth.

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Source
http://dx.doi.org/10.1039/c8lc00845kDOI Listing

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