Neuron Ball Formation

Neuron ball formation is a laboratory process in which neurons and associated neural cells assemble into compact, three-dimensional aggregates, providing a model of cellular organization beyond flat cultures. When dissociated cells are maintained in suspension or on low-adhesion surfaces, cell-cell adhesion, extracellular matrix interactions, and cytoskeletal remodeling drive clustering and compaction into a ball-like structure. These aggregates can support neurite outgrowth, cell-cell signaling, and the development of organized neuronal networks. In neuroscience, neuron balls help researchers study neural development, cellular survival, network formation, and responses to drugs or injury, while offering a more physiologically relevant platform for three-dimensional experimentation.

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JoVE EoE - Neuronal Culture Techniques

Developing Neuron Balls Using a Hanging Drop Culture Technique

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2025

This video demonstrates the process of generating neuron balls using a hanging drop culture technique. Within the hanging drops, cells move towards the bottom, self-assembled into three-dimensional structures forming neuron balls, which can be used for neurobiological studies.

Presynapse Formation Assay Using Presynapse Organizer Beads and “Neuron Ball” Culture

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Cited by 3 •

2019

Presynapse formation is a dynamic process including accumulation of synaptic proteins in proper order. In this method, presynapse formation is triggered by beads conjugated with a presynapse organizer protein on axonal sheets of “neuron ball” culture, so that accumulation of synaptic proteins is easy to be analyzed during presynapse formation.

Research

JoVE Journal - Developmental Biology
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An Optogenetic Approach for Assessing Formation of Neuronal Connections in a Co-culture System

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Cited by 20 •

2015

A protocol to generate a co-culture system consisting of neurons derived from induced pluripotent stem cells (iPSCs), primary cortical neurons and astrocytes is described. This co-culture system allows detection of the formation of synaptic contacts and circuits between new, iPSC-derived neurons and pre-existing cortical neurons expressing channelrhodopsin-2.

Initiating Rapid Neurite Extension and Formation Functional Neuronal Connections

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2025

This video demonstrates a technique for the rapid initiation and extension of a neuron and creation of new connections with a target neuron using a microfluidic device and micromanipulation. This could be used for therapies that aim to reconnect neuronal circuits after trauma or in neurodegenerative diseases.

Generating 3D Co-culture Spheres of Astrocytes and Neurons to Induce Synapse Formation

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2025

This video demonstrates a procedure for co-culturing the astrocytes and neurons to form 3D spheres. These 3D spheres provide a distinct platform for examining synapse formation and neural network integration, thereby serving as a potential model for research in developmental neuroscience, neurodegenerative diseases, and neuropharmacological interventions.

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