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Halmai, J.

Publications and source records attributed to Halmai, J..

2 recordsLinked to original sources

Cortical Organoid Model of PPP2R5D Genetic Intellectual Disability Models Disease Severity Phenotype

Jordans Syndrome (JS) is a rare, neurodevelopmental disorder caused by de novo missense mutations in protein phosphatase 2 regulatory subunit Bdelta (PPP2R5D). JS is characterized by severe neurological impairments starting in early life. PPP2R5D encodes for B56{delta}, one of the regulatory subunits of protein phosphatase 2A (PP2A). PP2A is a heterotrimeric protein serine/threonine phosphatase that is highly expressed in the brain and the liver. Past studies have focused on PP2As role in liver and little is known about the holoenzymes behavior in neuronal cells. Although B56{delta} is known to play an important role in the substrate specificity of PP2A, the identification of validated downstream substrates in JS remains unclear. To better understand how the mutations affect neuronal cells, we developed cerebral cortical-like organoids from an engineered allele series of the most common JS mutations to characterize the physiological changes throughout different stages of neurodevelopment. Organoids were assessed for transcriptomic, protein, and electrophysiological changes utilizing bulk RNA sequencing, immunocytochemistry, Western Blot, and high-density MicroElectrode Array. The results identify differentially expressed genes and translated proteins, potential neuronal substrates, and significant electrophysiological signatures that suggest mutations in B56{delta} lead to variant-specific dysfunction of PP2A. Overexpression of PPP2R5D through AAV transduction of organoids rescued several phenotypes in the variants, suggesting different pathogenetic etiology underneath. Our findings successfully characterized cerebral cortical-like organoids in JS cell lines and demonstrated its potential as a model for studying neurodevelopmental disorder and for screening therapeutic approaches.

cell biology↗

ZC4H2 loss of function is associated with temporal dysregulation of neural stem proliferation and neuron development

ZC4H2 is an X-linked zinc finger transcription factor essential for early neurodevelopment. Pathogenic variants in ZC4H2 are associated with both central and peripheral nervous system pathologies. The molecular and cellular mechanisms driving these phenotypes remain poorly understood, particularly in human female models that have undergone X chromosome inactivation. Neuronal models were differentiated from a human female cell line with a de novo Xq11.2 deletion causing ZC4H2 loss of function, associated with arthrogryposis multiplex congenita and cognitive impairment. Using iPSC-derived neural stem cells and cortical organoids, we identified premature neuronal differentiation, reduced BMP-SMAD signaling, and decreased SMAD1/5 phosphorylation. In cortical organoids, ZC4H2 deficiency altered neurogenesis timing, retaining proliferative progenitors while prematurely activating neuronal programs, leading to enlarged organoids with persistent dysregulation of gene programs required for complete neuronal maturation. We identified ZC4H2 target genes likely to mediate these phenotypes and tested a codon-optimized transgene showing both the restoration of SMAD1/5 phosphorylation, BMPR2 gene expression, and improved neuronal complexity. These results demonstrate effective ZC4H2 restoration in complex human models and highlight therapeutic potential for ZC4H2-linked neurodevelopmental disorders.

neuroscience↗