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Yates, F.

Publications and source records attributed to Yates, F..

4 recordsLinked to original sources

A robust and comprehensive quality control of cerebral cortical organoids: methodology and validation

Cerebral organoids hold great promise for neuroscience research as complex in vitro models that mimic human brain development. However, they face significant challenges related to quality and reproducibility, leading to unreliability in both academic and industrial contexts. Discrepancies in morphology, size, cellular composition, and cytoarchitectural organization limit their application in biomedical studies, particularly in disease modeling, drug screening, and neurotoxicity testing, where consistent models are essential. Critically, current methods for organoid characterization often lack standardization and rely heavily on subjective assessments, restricting their broader applicability. In this study, we developed a comprehensive Quality Control (QC) framework for 60-days cortical organoids. Five key criteria: morphology, size and growth profile, cellular composition, cytoarchitectural organization, and cytotoxicity, are evaluated using a standardized scoring system. We implemented a hierarchical approach, beginning with non-invasive assessments to exclude low-quality organoids (Initial Scoring), while reserving in-depth analyses for those that passed the initial evaluation (Final Scoring). To validate this framework, we exposed 60-day cortical organoids to graded doses of hydrogen peroxide (H2O2), inducing a spectrum of quality outcomes. The QC system demonstrated its robustness and reproducibility by accurately discriminating organoid quality based on objective and quantifiable metrics. This standardized and user-friendly framework for quality assessment not only minimizes observer bias but also enhances the reliability and comparability of cerebral organoid studies. Additionally, its scalability makes it suitable for industrial applications and adaptable to other organoid types, offering a valuable tool for advancing both fundamental and preclinical research.

neuroscience↗

Deciphering Neuronal Deficit and Protein Profile Changes in Human Brain Organoids from Patients with Creatine Transporter Deficiency

Creatine transporter deficiency (CTD) is an X-linked disease caused by mutations in the SLC6A8 gene. The impaired creatine uptake in the brain results in intellectual disability, behavioral disorders, language delay, and seizures. In this work, we generated human brain organoids from induced pluripotent stem cells of healthy subjects and CTD patients. Brain organoids from CTD donors had reduced creatine uptake compared with those from healthy donors. The expression of neural progenitor cell markers SOX2 and PAX6 was reduced in CTD derived organoids, while GSK3{beta}, a key regulator of neurogenesis, was up-regulated. Shotgun proteomics combined with integrative bioinformatic and statistical analysis identified changes in abundance of proteins associated with intellectual disability, epilepsy, and autism. Re-establishment of the expression a functional SLC6A8 in CTD-derived organoids restored creatine uptake and normalized the expression of SOX2, GSK3{beta} and other key proteins associated with clinical features of CTD patients. Our brain organoid model opens new avenues for further characterizing the CTD pathophysiology and supports the concept that reinstating creatine levels in patients with CTD could result in therapeutic efficacy. Summary HeadingTherapeutic targets associated with Creatine Transporter Deficiency

neuroscience↗

A 3-dimensional molecular cartography of human cerebral organoids revealed by double-barcoded spatial transcriptomics

Spatially-resolved transcriptomics is revolutionizing our understanding of complex tissues, but their current use for the exploration of a few sections is not representative of their 3-dimensional architecture. In this work we present a low-cost strategy for manufacturing molecularly double-barcoded DNA arrays, enabling large-scale spatially-resolved transcriptomics studies. We applied this technique to spatially resolve gene expression in several human brain organoids, including the reconstruction of a 3-dimensional view from multiple consecutive sections, revealing gene expression divergencies throughout the tissue.

systems biology↗

Antifungal activity of Cinnamomum cassia and Origanum compactum essential oils against Aspergillus oryzae

Aspergillosis is a nosocomial disease that usually affects the respiratory system. While most patients develop mild symptoms, aspergillosis can become a serious health threat in immunocompromised populations and patients with pre-existing respiratory conditions. Aspergillosis is caused by fungi of the Aspergillus genus. Existing treatments include drugs such as amphotericin B, with strong side effects. Numerous studies have shown the antifungal properties of essential oils (EOs), which represent potential alternative treatments against fungal infections. Here, we screened the antifungal properties of five EOs against Aspergillus oryzae: Melaleuca alternifolia, Mentha x piperita, Thymus zygis, Origanum compactum, and Cinnamomum cassia. Of the five EOs, two demonstrated antifungal activity: Origanum compactum acted as a fungistatic, while Cinnamomum cassia showed both fungistatic and fungicidal effects against A. oryzae. Therefore, both EOs represent potential alternative treatments against Aspergillosis.

microbiology↗