Our body 
transmits information throughout the body along neurons. Electrical 
signals are sent down neuronal axons which are insulated on the outside 
with myelin to ensure rapid conduction of information. Myelin is a 
lipid-rich structure which extends from the plasma membrane of glial 
cells.
Disruption of myelin production leads to devastating neuronal 
conditions such as multiple sclerosis (MS). Although our body has the 
ability to repair damaged myelin, in degenerative conditions this 
process of remyelination fails. As a result, it is of paramount 
importance to study the molecular and cellular mechanisms that 
co-ordinate myelin formation in order to understand how loss of myelin 
progresses to disease development.
In this context, scientists on the EU-funded 'Analysis of myelinated
 axon development in zebrafish' (ZEBRAFISH MYELIN) project used 
zebrafish as a model for studying myelin formation. Zebrafish constitute
 an ideal model due to small size, transparency and rapid development, 
enabling researchers to observe biological events at high resolution.
Through a series of transgenic animals, scientists were able to 
manipulate myelination and visualise the outcome. They discovered that 
individual axons regulate myelin sheath production by oligodendrocytes 
over a very short time. The research team also successfully elucidated 
how myelin forms around neuronal axons and identified new genes and 
regulator molecules of the process of myelination.
The ZEBRAFISH MYELIN project findings have clinical implications as 
they will improve our understanding of neuronal degeneration in MS, 
culminating in the identification of novel therapeutic targets. The 
zebrafish model could also be used for the pharmacological screening of 
small molecules with therapeutic potential.
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