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Methods in Neuronal Cell Culture

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Ramiro Almeida

Ramiro Almeida

University of Aveiro

Dr. Ramiro de Almeida is an Assistant Professor at the Department of Medical Sciences, University of Aveiro, Portugal. Prior to joining the University of Aveiro he was a Professor at the School of Health Sciences, Porto, Portugal. Dr. Almeida received his BSc in Biochemistry and a Ph.D. in Cell Biology from the University of Coimbra, and he carried out his post-doctoral studies at Weill Cornell Medical College, New York. His laboratory combines molecular, genetic, imaging and microfluidic tools to identify the intra-axonal mechanisms utilized by developing neurons to extend axons and form synaptic connections, which ultimately result in the proper wiring of the nervous system. He is also investigating how these mechanisms can be used under injury scenarios to promote neuronal regeneration.

Collection Overview

Neurons are the primary cells of the nervous system and are responsible for the distinctive roles of the brain. Understanding the mechanisms that regulate their differentiation, development, and function is essential to understand the nervous system and how it regulates other organs. Neuronal cell cultures can be prepared from various regions of the central and peripheral nervous system. Although this model has some limitations, for example, the lack of interactions with other cell types and the absence of the layered organization of the brain, neuronal cultures reproduce most of the key properties and distinct characteristics observed in vivo and are invaluable tools to study the nervous system.

Culturing nerve cells is still a challenging task, due to technical difficulties in isolating specific brain regions and the precise requirements of each neuronal population. Primary neuronal cultures are excellent models to study fundamental aspects of neuronal development and function like axonal growth, synapse formation, neurotransmission, and neuronal plasticity; to investigate intracellular trafficking and subcellular localization of endogenous proteins; to uncover the effect of disease-related mutations; to perform drug screens, disease modeling, and toxicological studies. In this collection, we present a variety of neuronal cell culture models, which are the result of the expertise of experienced researchers in each specific neuronal type. These protocols will provide detailed information about the methodology and the most relevant procedures used to cultured neuronal cells from the mammalian nervous system.

 

Articles

Isolation and Culture of Chick Ciliary Ganglion Neurons
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Isolation and Culture of Chick Ciliary Ganglion Neurons

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2020

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Abstracts

Two-Photon Polymerization 3D-Printing of Microfluidic Neuronal Culture Devices

Ali Hosseini1,

Giovanni Noselli2,

Michele Giugliano*1

1International School of Advanced Studies, Neuroscience Area, Trieste, Italy,

2International School of Advanced Studies, Mathematics Area, Trieste, Italy