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.