October 21, 2019 Poster Open Access

Maussion, Gilles; Rocha, Cecilia; Soubannier, Vincent

DCAT Export

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    <dct:title>Characterization of the activity-dependent development of IPSC-derived neurons from Fragile X patients</dct:title>
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    <dcat:keyword>induced pluripotent stem cells</dcat:keyword>
    <dcat:keyword>cortical neurons</dcat:keyword>
    <dcat:keyword>Fragile X</dcat:keyword>
    <dcat:keyword>Activity</dcat:keyword>
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    <dct:description>&lt;p&gt;Fragile X syndrome is a form of syndromic autism whose genetic causes have been relatively well uncovered. It is&lt;br&gt; actually mainly caused by a CGG triplet expansion in the 5&amp;rsquo; UTR sequence of FMR1 gene, affecting mostly men. FMR1&lt;br&gt; encodes a mRNA binding protein which is involved in the regulation of local translation at the synaptic level. The&lt;br&gt; mechanisms leading from such gene mutations to a neurodevelopmental disorder still need to be investigated. While&lt;br&gt; several studies have shown that the neuronal development is driven by cellular activity and connectivity, we aim to&lt;br&gt; further investigate the effect of FMR1 repression on the neuronal activity taking advantage of IPSC-derived neurons&lt;br&gt; from patient&amp;rsquo;s cells. IPSC-derived neurons will be investigated through calcium imaging to characterized their pattern&lt;br&gt; of spontaneous activities, as well as their capability to respond to neurotransmitter through extra-synaptic receptors.&lt;br&gt; A multielectrode array approach is going to be used to analyse the overall network activities. Those studies should&lt;br&gt; provide further information on the impairment of activity-dependent neuronal development in Fragile X syndrome.&lt;/p&gt;</dct:description>
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