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    Culture and transfection of iPSC-derived neurons for live-imaging of axonal cargoes

    Dan Dou, Erika L.F. Holzbaur, Alexander Boecker

    Published: 2023-05-24 DOI: 10.17504/protocols.io.x54v9dj4zg3e/v1
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    Abstract

    Here, we plate, culture, and transfect human iPSC-derived excitatory glutamatergic neurons for the purpose of observing transport of axonal cargoes under spinning disk confocal microscopy. Protocol is largely as previously described (Boecker et al., 2020, 2021; Fernandopulle et al., 2018). For preceding differentiation of neurons, see “Protocol: Piggybac-mediated stable expression of NGN2 in iPSCs for differentiation into excitatory glutamatergic neurons” and “Protocol: iNeuron differentiation from human iPSCs.”

    Attachments

    550-1146.pdf

    Steps

    Culture and transfection of iPSCderived neurons for live-imaging of axonal cargoes

    1.

    In advance, prepare 10x PLO stock.

    AB
    PLO50 mg
    0.1M borate buffer50 mL

    Note
    Store 10x PLO stock at -80°C.

    2.

    The day before plating, coat imaging dishes with 1x PLO solution (10x PLO stock diluted in ddH2O).

    Note
    It is only necessary to fully coat the glass center of the imaging dish.

    3.

    The day of plating, remove PLO solution from imaging dishes and wash twice with ddH2O.

    3.1.

    Add 2mL of iNeuron culture media.

    BrainPhys supplemented with

    AB
    BDNF10 ng/mL
    NT-310 ng/mL
    Laminin1 μg/mL
    B-27 supplement1x
    3.2.

    Place dishes in cell culture incubator for >0h 30m 0s.

    4.

    Rapidly thaw cryopreserved iNeurons in 37°C water bath.

    Note
    Retrieve vial to tissue culture hood when only a small amount of ice remains visible.

    5.

    Centrifuge to remove freezing media and resuspend cell pellet in iNeuron culture media.

    BrainPhys supplemented with

    AB
    BDNF10 ng/mL
    NT-310 ng/mL
    Laminin1 μg/mL
    B-27 supplement1x
    6.

    Count cells and plate 300k neurons per 35 mm imaging dish.

    6.1.

    Add cells dropwise to the center area of the dish (so that they sink onto the glass, PLO-coated center).

    7.

    For Piggybac-delivered NGN2 neurons, include 10micromolar (µM) 5-Fluoro-2′-deoxyuridine and 10micromolar (µM) uridine at the time of plating to prevent survival of mitotic cells.

    Note
    These drugs were removed 24 hours after plating.

    8.

    Store neurons in cell culture incubator. Perform partial change of iNeuron media twice per week.

    9.

    On DIV18 (~72h 0m 0s prior to imaging), transfect iNeurons for imaging.

    Note
    Transfection conditions may require optimization, but a typical transfection will use 4µL Lipofectamine Stem and 1µg of plasmid DNA. Plasmids with the PGK or EF1α promoters express best in iNeurons.

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