Muriel Perron

@murielperron.bsky.social

CNRS researcher interested in neural stem cells, retina, and regeneration

#SdC2026 Retrouvez Carole Escartin, cheffe d'équipe à NeuroPSI, dans une table ronde et plusieurs reportages de ‪@glialclub.bsky.social sur le rôle des cellules gliales dans la maladie d’Alzheimer, dans a cadre de la semaine du cerveau ! 🔽🔽🔽

French Glial Cell Club@glialclub.bsky.social · 5mo ago

Pour la Semaine du Cerveau #SdC2026 le Club des Cellules Gliales et France #Alzheimer ont concocté pour vous une immersion dans trois laboratoires et une table ronde pour vous plonger au cœur de la recherche et mieux comprendre le rôle des cellules gliales. Replay : www.youtube.com/watch?v=5v5z...

Happy to announce that our latest paper is now out! Have you ever wondered how neural tissues control their size? In this paper, we show that cell division orientation is critical in both the cortex and retina. www.science.org/doi/10.1126/...

Oriented cell divisions induce basal progenitors and regulate neural expansion across tissues and species

A fundamental role for division orientation in progenitor output driving cortical and retinal growth is revealed.

science.org

👏 Upcoming seminars at NeuroPSI in January (11:30am): ➡️ The 23rd, Marc Dhenain, Institut de Biologie François Jacob, "Pseudo-prions to treat neurodegenerative diseases." Followed by two speakers on motor control: ➡️ The 27th, Maarten Zwart, from St Andrews. ➡️ The 30th, Graziana Gatto, from Cologne.

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The lab's first paper of the new year is out. In it, we investigate the role of the late stage retinal progenitor-enriched SoxE family factors Sox8 and Sox9 in controlling retinal development./1 www.biorxiv.org/content/10.6...

Sox8 and Sox9 regulate differentiation and nuclear positioning of retinal Müller glia

Temporal patterning of retinal progenitor cells governs the sequential generation of retinal cell types, with gliogenesis occurring late in development. Sox8 and Sox9, members of the SoxE transcription factor family, are highly expressed in late-stage retinal progenitor cells and mature Müller glia, yet their functional roles remain incompletely defined. Here we employed gain- and loss-of-function approaches, single-cell multiomic profiling, and injury models to investigate Sox8/9 function. Overexpression of SOX8 and/or SOX9 in early-stage retinal progenitor cells suppressed early-born cell fates and promoted photoreceptor generation, consistent with a role in late-stage temporal identity. Conversely, conditional deletion of Sox8 and/or Sox9 in late-stage progenitors did not impair Müller glia specification, but caused radial displacement of Müller glia nuclei into the outer retina and modest changes in glial gene expression. Loss of Sox8/9 in mature Müller glia modestly increased proliferation post-injury without inducing neurogenic competence. These findings suggest that Sox8/9 are dispensable for gliogenesis and repression of neurogenic competence, but are essential for proper laminar positioning and maturation of retinal Müller glia. ### Competing Interest Statement S.B. is a cofounder, shareholder, and scientific advisory board member of CDI Labs LLC, and receives research support from Genentech. National Eye Institute, https://ror.org/03wkg3b53, R01EY036173

biorxiv.org

🚨We are recruiting two PhD students 🚨 1) Quantitative & dynamic analysis of limb-regenerative signaling centers w/ @osvaldo-chara.bsky.social 📶🧮💻 🔗https://www.phd.tuebingen.mpg.de/80704/Quantitative-and-dynamic-analysis-of-limb-regenerative-signaling-center-interactions