Neural peer pressure: intercellular dynamics and emergent phenotypes in the mosaic Rett syndrome brain

During female embryogenesis, each cell randomly inactivates either the maternal or paternal X chromosome, creating a natural mix, or mosaic, of cells with a different active X chromosome. In X-linked neurological disorders such as Rett syndrome, this results in a brain composed of two cell populations: one expressing the mutant allele and one expressing the wildtype allele. Rather than behaving as independent entities, these populations influence one another through the exchange of extracellular vesicles, free-floating biomolecules, and direct cell-cell contacts. The bidirectional communication between mutant and wildtype cells can give rise to emergent behaviors that cannot be explained by cell-autonomous mechanisms alone. Particularly, rather than a simple dichotomy of two discrete cell states, emerging evidence suggests that the mosaic Rett syndrome brain contains a spectrum of cells with intermediate phenotypes. Hence, shifting focus from isolated cellular effects to cell population-level dynamics will be crucial for advancing our understanding of mosaic conditions and developing effective therapeutic strategies.

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Publication Details

Journal
Cell Communication and Signaling
Published
2026-06-16
DOI
https://doi.org/10.1186/s12964-026-02987-w
Primary Topic
Genetics and Neurodevelopmental Disorders
Type
article
Field-Weighted Citation Impact
0.00
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article

Neural peer pressure: intercellular dynamics and emergent phenotypes in the mosaic Rett syndrome brain

Leopold Curfs, Lars Eijssen, Jarno Koetsier, Chris P. Reutelingsperger et al.
Cell Communication and Signaling
Genetics and Neurodevelopmental Disorders
article

Neural peer pressure: intercellular dynamics and emergent phenotypes in the mosaic Rett syndrome brain

Leopold Curfs, Lars Eijssen, Jarno Koetsier, Chris P. Reutelingsperger, Nasim Bahram Sangani
article en

Abstract

During female embryogenesis, each cell randomly inactivates either the maternal or paternal X chromosome, creating a natural mix, or mosaic, of cells with a different active X chromosome. In X-linked neurological disorders such as Rett syndrome, this results in a brain composed of two cell populations: one expressing the mutant allele and one expressing the wildtype allele. Rather than behaving as independent entities, these populations influence one another through the exchange of extracellular vesicles, free-floating biomolecules, and direct cell-cell contacts. The bidirectional communication between mutant and wildtype cells can give rise to emergent behaviors that cannot be explained by cell-autonomous mechanisms alone. Particularly, rather than a simple dichotomy of two discrete cell states, emerging evidence suggests that the mosaic Rett syndrome brain contains a spectrum of cells with intermediate phenotypes. Hence, shifting focus from isolated cellular effects to cell population-level dynamics will be crucial for advancing our understanding of mosaic conditions and developing effective therapeutic strategies.

Cell Communication and Signaling
Maastricht University Medical Centre (NL), Maastricht University (NL)
Openalex Percentile: Top 8%
Genetics and Neurodevelopmental Disorders
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