Establishing a human cell model of the glial dysfunction in multiple sclerosis

Degree type


Closing date

18 July 2022



Citizenship requirement


About the research project

Multiple Sclerosis (MS) is a complex disease associated with immune cell infiltration of the central nervous system (CNS), myelin loss, and neurodegeneration. The exact cause of MS is not known, but knowledge of the key lifestyle, environmental and genetic risk factors has led to the development of 2 competing hypotheses – (i) the ‘inside-out’ hypothesis where MS starts in the CNS and leads to the activation of the peripheral immune system, and (ii) the ‘outside-in’ hypothesis where the immune system is activated peripherally and attacks the CNS. To investigate the ‘inside out’ hypothesis we will use stem cell lines produced by reprogramming blood cells from people with MS to generate key brain cell types – namely, oligodendrocytes, astrocytes, microglia, and neurons—and perform RNA sequencing and cell biology assays (e.g. flow cytometry, biochemistry, immunocytochemistry, enzyme-linked immunosorbent assays (ELISAs), confocal microscopy and image analysis) to understand the earliest contribution of brain cells to propagating MS pathology. We anticipate that this project will result in the first ever in vitro model of MS that will enable us to learn the cellular pathways that are responsible for MS initiation and progression, and provide a novel platform for the development of brain repair therapies. The student will work within the MS Research Flagship and be supported by an interdisciplinary team consisting of world-leading experts in glial and stem cell biology, genomics, and MS pathophysiology. We expect that the outcomes from this project will result in the identification of pathways that can be targeted for therapeutic intervention that will feed into our fundamental research to clinical trial pipeline.

**Multiple students can undertake different aspects of this project, and the co-supervisory team can be finalised following a discussion with A/Prof Young.

Primary Supervisor

Meet A/Prof Kaylene Young


Applicants will be considered for a Research Training Program (RTP) scholarship or Tasmania Graduate Research Scholarship (TGRS) which, if successful, provides:

  • a living allowance stipend of $28,854 per annum (2022 rate, indexed annually) for 3.5 years
  • a relocation allowance of up to $2,000
  • a tuition fees offset covering the cost of tuition fees for up to four years (domestic applicants only)

If successful, international applicants will receive a University of Tasmania Fees Offset for up to four years.

As part of the application process you may indicate if you do not wish to be considered for scholarship funding.


Applicants should review the Higher Degree by Research minimum entry requirements.

Selection Criteria

The project is competitively assessed and awarded.  Selection is based on academic merit and suitability to the project as determined by the College.

Additional essential selection criteria specific to this project:

  • A BSc (Hons) degree or equivalent

Additional desirable selection criteria specific to this project:

  • A background in neuroscience would be advantageous
  • Experience working in a laboratory

Application process

There is a three-step application process:

  1. Select your project, and check you meet the eligibility and selection criteria;
  2. Contact the Primary Supervisor, A/Prof Kaylene Young to discuss your suitability and the project's requirements; and
  3. Submit an application by the closing date listed above.
    • Copy and paste the title of the project from this advertisement into your application. If you don’t correctly do this your application may be rejected.
    • As part of your application, you will be required to submit a covering letter, a CV including 2 x referees and your project research proposal.

Following the application closing date applications will be assessed within the College. Applicants should expect to receive notification of the outcome by email by the advertised outcome date.

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