A monitoring system for axonal growth dynamics using micropatterns of permissive and Semaphorin 3F chemorepulsive signals

Jae Ryun Ryu, June Hoan Kim, Hyo Min Cho, Youhwa Jo, Boram Lee, Sunghoon Joo, Uikyu Chae, Yoonkey Nam, Il Joo Cho, Woong Sun

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)


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.

Original languageEnglish
Pages (from-to)291-305
Number of pages15
JournalLab on a Chip
Issue number2
Publication statusPublished - 2019 Jan 21

Bibliographical note

Funding Information:
This research was supported through the National Foundation of Korea (NRF), funded by the Ministry of Science, ICT & Future Planning (NRF-2016R1D1A1B01011346, NRF-2017M3A9B3061308, NRF-2015M3C7A1028790, NRF-2016R1A6A3A01009971). We thank Dr. Bokkee Eun at the Core Laboratory for Convergent Translational Research, College of Medicine, Korea University for helpful discussion, and members of the Sun laboratory for sharing the reagents.

Publisher Copyright:
© The Royal Society of Chemistry.

ASJC Scopus subject areas

  • Bioengineering
  • Biochemistry
  • General Chemistry
  • Biomedical Engineering


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