A novel tool that embeds 3Rs principles in multiple sclerosis research

Multiple sclerosis (MS) is the most common cause of nontraumatic neurological disability in young adults in Europe and North America. This debilitating disease is modelled in animals by inducing central nervous system (CNS) autoimmunity in which the animal's defence system against bacteria and viruses, instead attacks cells in the animal's CNS. This results in experimental autoimmune encephalomyelitis (EAE); a condition characterised by paralysis in the experimental animal. Thus, EAE is classed as severe under the Animals (Scientific Procedures) Act 1986. Although EAE has helped us understand aspects of MS and informed drug discovery and testing, there is an urgent need to find an alternative that eliminates or reduces its use. Here we will develop and verify a cell culture (brain in a dish) model of EAE to replace experiments in living animals.

With our combined expertise in EAE, myelinating cell cultures, axon degeneration and electrophysiology, we will provide a validated cell culture tool to:

  • Model EAE/MS using embryonic mice, that (i) reduces the use of EAE by the research and pharmaceutical communities (ii) will be used to generate new concepts, ideas, toxicity screening and target validation and (iii) to investigate how axons are injured and can be rescued in the context of progressive MS.
  • Publicise this model to maximise its uptake
  • Provide training in the 3Rs principles in general, and in the context of understanding, investigating and identifying therapies for neurodegenerative disorders.
  • Instil a long-term appreciation and adoption of the 3Rs principles
  • Elucidate the mechanisms and molecules responsible for axon injury, providing rationale targets for therapeutic intervention.
  • Provide mentoring and training in many skills, including adoption of rigorous and unbiased approaches to addressing research questions.

The model will be amenable to:

  • Electrophysiological analysis which replace the EAE disability score for testing the benefits/toxicity of putative therapeutics.
  • Screening up to 180 molecules simultaneously for axon protection properties, using immunocytochemistry and a 96-well format
  • Single cell transcriptomic analysis, immunohistochemistry, western blotting, qRT-PCR, ELISA and other assays to provide mechanistic insights in basic research applications.
  • The model cannot replace all in vivo work, but it will be particularly useful in testing therapies for progressive forms on MS in which CNS-intrinsic processes are principal contributors to disability progression. More details on 3Rs benefits are detailed in the supporting information.

The PhD student will receive practical and theoretical training in 3Rs principles throughout the duration of the studentship from Biological Services staff including qualified veterinarians, animal care staff and the Dr Edgar, who has almost 20 years hands-on experience in a wide range of procedures, training and reporting.

We will provide ‘hands-on’ training as required and also detailed written instructions and videos if hands-on training is not feasible, making adoption straight forward. The model cannot fully replicate the in vivo situation involving the gut microbiome, peripheral and/or adaptive immune system, vasculature and endocrine systems, but conversely, this limitation allows uncoupling of CNS-intrinsic molecules and mechanism to address important questions, such as what drives progression in progressive forms of MS.

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PhD Studentship

Status:

Inactive

Principal investigator

Dr Julia Edgar

Institution

University of Glasgow

Co-Investigator

Professor Christopher Linington

Grant reference number

NC/T002247/1

Award date:

Jan 2020 - Jan 2023

Grant amount

£90,000