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Arnold, V.

Publications and source records attributed to Arnold, V..

2 recordsLinked to original sources

3R-Compliant Murine Ex Vivo Platform for Scalable Brain Cancer Modeling and Drug Screening

Translating in vitro findings into in vivo applications remains a major challenge in brain cancer drug discovery, largely due to inadequate models for assessing neurotoxicity and tumor microenvironment (TME) dynamics. Here, we present a novel, highly modular murine ex vivo platform based on adult neural stem cells (aNSCs), designed for scalable, medium-throughput drug screening and mechanistic studies for brain cancer research. This system integrates progressive 2D and 3D models, including assembled models for tumor migration, cancer core models mimicking tumor localization within neural tissue and advanced cancer core models incorporating immune cells to recapitulate key TME interactions. With high reproducibility, defined cell composition and rapid formation within 72 hours, these assembloids provide a translationally relevant and ethical alternative to animal models. Aligned with 3R principles, this platform bridges the gap between in vitro and in vivo studies, offering a powerful tool for innovating brain cancer drug discovery.

cancer biology↗

Early Disruption of Photoreceptor Cell Architecture and Loss of Vision in a Humanized Pig Model of Usher Syndrome

Usher syndrome (USH) is the most common form of monogenic deaf-blindness. Loss of vision is untreatable and, so far, there are no suitable animal models for testing therapeutic strategies. By introducing a human mutation into the harmonin-encoding USH1C gene in pigs, we generated the first translational animal model for USH type 1 with characteristic hearing defect, vestibular dysfunction and visual impairment. Changes in photoreceptor architecture, quantitative motion analysis and electroretinography were characteristics of the reduced retinal virtue in USH1C pigs. Primary cells from those animals and USH1C patients showed significantly elongated primary cilia, compared to wild-type, confirming the nature of USH as a true and general ciliopathy and proving the therapeutic capacity of gene supplementation and gene repair approaches.

genetics↗