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High-content analysis of neuronal morphology in human iPSC-derived neurons.

STAR protocols (2022-08-23)
Selene Lickfett, Carmen Menacho, Annika Zink, Narasimha Swamy Telugu, Mathias Beller, Sebastian Diecke, Sidney Cambridge, Alessandro Prigione
ZUSAMMENFASSUNG

We present a high-content analysis (HCA) protocol for monitoring the outgrowth capacity of human neurons derived from induced pluripotent stem cells (iPSCs). We describe steps to perform HCA imaging, followed by quantifying the morphology of dendrites and axons within a high-throughput system to evaluate neurons obtained through various differentiation approaches. This protocol can be used to screen for modulators of neuronal morphogenesis or neurotoxicity. The approach can be applied to patient-derived iPSCs to identify patient-specific defects and possible therapeutic strategies. For complete details on the use and execution of this protocol, please refer to Zink et al. (2020) and Inak et al. (2021). The protocol can be used in combination with Zink et al. (2022).

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Produktbeschreibung

Sigma-Aldrich
Laminin aus Engelbreth-Holm-Swarm murine sarcoma basement membrane, 1-2 mg/mL in Tris-buffered saline, 0.2 μm filtered, BioReagent, suitable for cell culture
Sigma-Aldrich
Albumin aus Rinderserum, heat shock fraction, pH 7, ≥98%
Sigma-Aldrich
Cytosin β-D-Arabinofuranosid, crystalline, ≥90% (HPLC)
Sigma-Aldrich
Anti-Guinea Pig IgG (H+L), highly cross-adsorbed, CF 488A antibody produced in donkey, ~2 mg/mL, affinity isolated antibody