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bioRxiv · 10.1101/2024.01.25.577271

Dual effects of ARX poly-alanine mutations in human cortical and interneuron development

Abstract

Infantile spasms, with an incidence of 1.6 to 4.5 per 10,000 live births, are a relentless and devastating childhood epilepsy marked by severe seizures but also leads to lifelong intellectual disability. Alarmingly, up to 5% of males with this condition carry a mutation in the Aristaless-related homeobox (ARX) gene. Our current lack of human-specific models for developmental epilepsy, coupled with discrepancies between animal studies and human data, underscores the gap in knowledge and urgent need for innovative human models, organoids being one of the best available. Here, we used human neural organoid models, cortical organoids (CO) and ganglionic eminences organoids (GEO) which mimic cortical and interneuron development respectively, to study the consequences of PAE mutations, one of the most prevalent mutation in ARX. ARXPAE produces a decrease expression of ARX in GEOs, and an enhancement in interneuron migration. That accelerated migration is cell autonomously driven, and it can be rescued by inhibiting CXCR4. We also found that PAE mutations result in an early increase in radial glia cells and intermediate progenitor cells, followed by a subsequent loss of cortical neurons at later timepoints. Moreover, ARX expression is upregulated in COs derived from patients at 30 DIV and is associated with alterations in the expression of CDKN1C. Furthermore, ARXPAE assembloids had hyperactivity which were evident at early stages of development. With effective treatments for infantile spasms and developmental epilepsies still elusive, delving into the role of ARXPAE mutations in human brain organoids represents a pivotal step toward uncovering groundbreaking therapeutic strategies.

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BibTeXRIS

Nieto-Estevez, V., Varma, P., Mirsadeghi, S., Caballero, J., Gamero-Alameda, S., Hosseini, A., Goswami, S., Silvosa, M. J., Thodeson, D. M., Lybrand, Z. R., Giugliano, M., Navara, C., Hsieh, J.. 2024-01-25. Dual effects of ARX poly-alanine mutations in human cortical and interneuron development. https://doi.org/10.1101/2024.01.25.577271

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