FP7Reintegration grant2010–2014

ZEBRAFISH MYELIN · Analysis of myelinated axon development in zebrafish

FP7 — People (Marie Curie Actions)

Duration
2010-05-01 → 2014-04-30
EU contribution
€100,000
Participants
1
Scheme
MC-IRG

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Results in brief

Analysis of myelinated axon development in zebrafish

The majority of axons in our nervous systems are wrapped by a lipid rich structure called the myelin sheath that is made by specialised glial cells. Myelin provides electrical insulation to axons, facilitates rapid energy-efficient nerve conduction, and is essential for long-term nervous system health. Disruption to myelin contributes to the symptoms of numerous devastating conditions, including the demyelinating disease multiple sclerosis, MS. Although our nervous systems have some ability to repair damaged myelin, this process, called remyelination, eventual fails, which leads to the axonal and neuronal degeneration associated with currently untreatable stages of MS. Dr. Lyons’s European Commission International Reintegration project was to perform an “Analysis of myelinated axon development in zebrafish”. Zebrafish are an incredibly powerful model for the study of myelinated axons for several reasons. The small size, optical transparency, relative simplicity, and rapid development of zebrafish embryos, means that biological events can be observed at high resolution as they occur in the living animal. During the period of Dr. Lyons’s International Reintegration Grant, his laboratory generated a suite of transgenic animals to directly visualise and manipulate myelination in the living zebrafish. With these tools they showed that individual axons regulate myelin sheath production by oligodendrocytes, that individual oligodendrocytes generate their myelin sheaths during a very short period of only a few hours and they elucidated how the myelin sheath itself is “wrapped” around those axons. As an indication of the general importance of the laboratory’s reagents, they have shared tools with >40 laboratories worldwide to date. Zebrafish are also the preeminent vertebrate laboratory model system with which one can carry out large-scale genetic and chemical “screens” to test in a systematic and high-throughput manner how manipulation of different genes or by using chemical compounds can affect biological processes of interest. During his IRG, Dr. Lyons initiated a new genetic screen at the University of Edinburgh and identified new genes required for myelination, and continues to identify more. The group also established platforms to carry out chemical screens to identify chemical compounds that can regulate and promote myelination, with a view to using this information to commence drug development projects for the treatment of diseases such as MS. The work carried out during Dr. Lyons’s IRG lead to numerous new avenues of funding, most recently to the award of long-term funding from the Wellcome Trust, by way of a Senior Research Fellowship in Basic Biomedical Science. Dr. Lyons has also established numerous exciting collaborations, both within the University of Edinburgh and the UK, with prominent European and internationally renowned scientists, and with the major MS drug developer Biogen Idec. Most importantly, during his IRG funding period Dr. Lyons has established a vibrant research group, and has established himself as an internationally recognised leader in the study of myelinated axons.

Data: CORDIS, © European Union

Project objective

Myelinated axons are an essential component of the vertebrate nervous system. Myelin is a plasma membrane extension of specialised glial cells that wraps around axons to facilitate the rapid conduction of neuronal impulses. Disruption of myelinated axons contributes to the symptoms of numerous human diseases, such as Multiple Sclerosis (MS). Our understanding of the molecular and cellular mechanisms that co-ordinate myelin formation and those that contribute to the progression of human diseases of myelinated axons such as MS remain rudimentary. We have helped establish the zebrafish as a powerful laboratory organism with which to dissect myelin formation. Through a forward genetic screen we identified ten genes essential normal myelinated axon formation. We identified new roles for genes previously implicated in myelinated axon development, isolated two completely novel regulators and identified mutations in four genes relevant to human diseases of myelinated axons. Disruption to the human homologue of one of those genes, kif1b, was recently associated with MS, and our initial studies identified important roles for this protein in myelinated axon formation. In this proposal we ask for support to continue our analysis of kif1b function. Although our genetic screen was a success it did not approach saturation and additional screens would clearly identify other factors essential for myelinated axon development. Gene discovery screens, however, take a long time to carry out, are quite labour intensive and can preclude the identification of mutations in genes required for multiple stages of development. In this proposal we outline novel methodologies to identify protein function in biological processes of interest by combining high-throughput screening of the phenotypic effects of small molecules on zebrafish with cutting edge technology to identify the protein targets of compounds that exert interesting effects.

Original text from CORDIS.

Participants

Links

Data: CORDIS, © European Union