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Baquerre, C.

Publications and source records attributed to Baquerre, C..

3 recordsLinked to original sources

The NaaS Methodology applied to modeling chemotherapy-induced peripheral neuropathy with human hiPSC neurons

The Neuron-as-a-Sensor (NaaS) methodology is a human-relevant platform designed to detect compound-induced effects by capturing functional changes in neuronal activity. This is achieved by integrating hiPSC-derived neuronal cultures, compartmentalized MEA microfluidic devices, a detailed electrophysiology paradigm and a standardized analysis pipeline. Applied to chemotherapy-induced peripheral neuropathy (CIPN), NaaS leverages electrophysiological profiling to capture alterations in neuronal excitability beyond cytotoxicity. Using paclitaxel and oxaliplatin as reference compounds, we demonstrated drug-specific, time-dependent changes in spontaneous and thermally evoked activity that align with their distinct clinical neuropathic phenotypes. Dimensionality reduction of electrophysiological metrics enabled construction of a functional discrimination map, allowing robust separation of compound signatures from vehicle controls. These findings highlight the ability of NaaS to model clinically relevant neurotoxic effects in a scalable manner, supporting its application in both adverse effect prediction and therapeutic screening.

bioengineering↗

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↗

Reprogrammed Pteropus Bat Stem Cells Present Distinct Immune Signature And Are Highly Permissive For Henipaviruses

Bats are unique among mammals due to the ability of powered flight and exceptional longevity. They are also asymptomatic hosts for numerous viruses, including recently emerged zoonotic Henipaviruses Nipah and Hendra, which are highly pathogenic for humans and other mammals. Better understanding of how bats control viral infection requires development of relevant permissive cellular experimental models. By applying a somatic reprogramming protocol to Pteropus bat primary cells, using a novel combination of ESRRB, CDX2, and c-MYC transcription factors, we generated bat reprogrammed cells exhibiting stem cell-like characteristics and a neural stem cell-like molecular signature. These cells present a unique interferon-stimulated transcriptomic signature and both produce and respond to interferon type-I, highlighting differences between stem cells from bats and other mammals. In contrast to primary bat cells, these reprogrammed cells are highly susceptible to infection by Henipavirus, thereby enabling isolation of new bat viruses, study of virus-bat interactions, and better understanding of bat biology. Summary sentenceSomatic reprogramming provides new bat stem cells with unique immune properties and original viral permissivness

cell biology↗