Fauna em Foco Science

Afshar-Saber W, Gasparoli FM, Yang Z, Teaney NA, Hobson R, Lalani L, Srinivasan G, Whye D, Karmakar R, Buttermore ED, Winden KD, Chen C, Sahin M. · Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026

An Open-Source Pipeline for Calcium Imaging and All-Optical Physiology in Human Stem Cell-Derived Neurons.

Sem tradução ainda. Este artigo está no acervo com licença aberta, mas o resumo em português ainda não foi gerado.

Resumo original em inglês

High-throughput, single-cell resolution profiling of neuronal activity is critical for understanding brain function and modeling neurological disorders, yet existing approaches are often limited by scalability and manual workflows. Here, we present an open-source, scalable imaging and analysis platform that integrates optogenetic stimulation, calcium imaging, automated acquisition, single-cell and network analyses. The platform enables robust quantification of spontaneous and evoked neuronal activity across hundreds of human stem cell-derived neurons over multiple timepoints, supporting functional phenotyping at both cellular and network levels. We demonstrate the versatility of the platform across multiple disease-relevant contexts, including models of CDKL5 Deficiency, SSADH Deficiency, and tuberous sclerosis complex (TSC). Additionally, we generate CRISPR-Cas9 knock-in hiPSC lines expressing GCaMP6s and demonstrate partial reversal through pharmacological intervention in TSC. By linking single-cell dynamics to network-level measures, this platform provides a generalizable framework for scalable functional phenotyping and high-throughput screening in human neuronal models.

Fonte e licença. Publicado sob CC BY. DOI: 10.1002/advs.202515887. Ler o artigo completo na fonte ↗

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Dados de terceiros. Metadados bibliográficos do Europe PMC, DOAJ, Crossref e OpenAlex. Taxonomia do GBIF — Global Biodiversity Information Facility, Backbone Taxonomy sob CC BY 4.0.

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