Research Update March 2016

Posted - February 2016 in HSPRF News

Progress report from the research team

 

Dr. Yongjun Fan

Dr. Yongjun Fan

Mouse project

 

In December, we reported the successful establishment of the different types of mouse cortical neurons from mouse brain tissue. This process has been further refined and optimised over the last quarter, with the identity of morphologically differentiated neurons confirmed using immunostaining tests for several neuron-specific proteins.

 

The breeding program is proceeding well, allowing new cultures of mouse brain tissue to be established each week since the start of the year. With the six-week differentiation period, this means that differentiated neurons are now coming online and available for analysis on a weekly basis since mid-February.

 

These neurons are now being investigated using automated image analysis methods to quantify the expression of acetylated alpha-tubulin and for the intracellular distribution of peroxisomes and mitochondria.

 

Fan has also been investigating the expression of certain proteins in the brains of the adult mice with different genotypes – normal, heterozygous and homozygous for the SPG4 mutation. He has quantified the same proteins investigated in the SPAST patient-derived olfactory stem cells – SPG4 (SPAST), SPG3A, STMN, and acetylated-alpha tubulin.

Once these baseline quantifications of HSP mouse neurons have been completed, the next step will be drug testing on them.

Dr. Gautam Wali

Dr. Gautam Wali

 

iPSC project

 

Following on from the December report of the successful establishment of induced pluripotent HSP stem cells (iPSCs) from an HSPer with a SPAST (SPG4) mutation, the first batch of cells have now been successfully differentiated into corticospinal neurons.

This batch has been used as quality control to confirm the identity of the neurons and to confirm that neurons could be generated both from the HSPer and from 2 unaffected people. The neurons passed the quality control tests. This is a major milestone.

The process to differentiate neurons in iPSC cultures takes 8 weeks. Regular batches of iPSC cultures have been established with the goal of providing ongoing availability of differentiated neurons for analysis. These neurons derived from human tissue will undergo almost identical analysis to the mouse neurons as described in the Mouse project report.

 

Comments on this story

  1. Grant posted at 1:52 pm on 2 March 2016Reply

    This sounds great a step closer! I like everyone will be awaiting further updates. Fantastic Grant

  2. SALVATORE posted at 8:35 am on 6 March 2016Reply

    … translated from Italian:
    I get the feeling that fairly soon a countdown will start… for something really fantastic.

    HO LA NETTA SENSAZIONE CHE TRA NON MOLTO INIZIERA’ IL CONTO ALLA ROVESCIA…. PER QUALCOSA DI FANTASTICO.

  3. Brenda posted at 9:45 pm on 8 March 2016Reply

    Go Australia! I am so happy you are making progress with HSP research. I am hoping and praying treatments will be here soon. Hopefully in my lifetime. I am 41, so I hope so ! Thanks to you all!

  4. Nick posted at 8:53 pm on 20 May 2016Reply

    I have been following your research for a while now and wondering if the clinical trials will also be going on in the USA ?

    • Editor posted at 11:18 am on 21 May 2016Reply

      Editor’s Note: The planning process for clinical trials is only just beginning, so the USA is a possibility. When the time comes, there will be global publicity and communications to the HSP community everywhere, letting everyone know what is going on.

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