1. MK SPORTS集团(中国)

    Cell culture, transfection, immunocytochemistry, and imaging

    Pietro De Camilli, Nisha Mohd Rafiq

    Published: 2024-03-19 DOI: 10.17504/protocols.io.5qpvokx3bl4o/v1
    AI 解读
    浏览 1509

    Abstract

    This protocol describes the maintenance, transfection, immunocytochemistry, and imaging of RPE1 and also transfection, immunocytochemistry, and imaging of iPSCs, i3Neurons and DA neurons.

    Attachments

    Rafiq_transfection_imaging.docx

    Steps

    General cell culture for RPE1

    1.

    Grow hTERT-RPE1 cells in DMEM/F12 (Thermo Fisher Scientific) supplemented with 10% FBS (Thermo Fisher Scientific), 1% glutaMAX, 1% penicillin-streptomycin. Keep cells at 37°C with 5% CO2 in an enclosed incubator.

    Note
    For general maintenance, when cells reach 80-90% confluency, detach them from the dish with Trypsin and dilute 1:10-20 in a new dish.

    Cell transfection for RPE1

    2.

    For live-cell imaging experiments, seed the cells on glass-bottom dishes (MatTek; 35mm) at the concentrations ranging from 1-2 × 105 cells.

    3.

    For RPE1: allow the cells to adhere for8h 0m 0s-24h 0m 0sbefore being transiently transfected using 4µL Lipofectamine™ 2000 Transfection Reagent (Invitrogen) in Opti-MEM media, mix them with the respective plasmids (1µg -2µg) and visualize after 48h 0m 0s.

    4.

    For cilia generation, serum-starve the cells in DMEM/F12 media (without FBS) for 48h 0m 0s.

    Cell transfection for iPSCs, i3Neurons and DA Neurons

    5.

    For live-cell imaging experiments, seed cells on glass-bottom dishes (MatTek; 35mm) at the concentrations ranging from 3-5 × 105 cells.

    6.

    Use2.4µL of Lipofectamine™ Stem Transfection Reagent (Invitrogen) in Opti-MEM media with respective plasmids (1µg-3µg) and visualize at least 48h 0m 0s later.

    Immunocytochemistry of RPE1, iPSCs, i3Neurons and DA Neurons

    7.

    For fixed-cell imaging experiments, seed cells on glass-bottom dishes (MatTek; 35mm) at the concentrations ranging from 1-3 x 105cells.

    • For immunofluorescence visualization, fix the cells with 4% (v/v) paraformaldehyde (Electron Microscopy Sciences) in 1× phosphate-buffered saline (PBS) for 0h 20m 0s.
    8.

    Wash cells thrice in PBS.

    9.

    Perform cell extraction with 0.25-0.5% (v/v) Triton X-100 in PBS for 0h 10m 0s.

    10.

    Wash cells thrice in PBS.

    11.

    For removal of free aldehyde groups, quench the cells with fresh1sodium borohydride (Sigma-Aldrich) in PBS for 0h 7m 0s, and then wash thrice in PBS.

    12.

    Further block the cells for 0h 30m 0s in 5% bovine serum albumin (BSA, Sigma-Aldrich) in PBS and then incubate 0h 10m 0s at 4°C with the respective antibodies listed in Table S1.

    13.

    Wash the cells with PBS thrice the following day and incubate with Alexa Fluor-conjugated secondary antibodies (Thermo Fisher Scientific) for 1h 0m 0s at Room temperature.

    14.

    Wash the cells thrice in 1×PBS.

    15.

    Use DAPI (Thermo Fisher Scientific) for nuclear staining, when necessary.

    Imaging

    16.

    For live imaging, maintain cells in a caged incubator with humidified atmosphere (5% CO2) at 37°C.

    Note
    The Yokogawa spinning disk field scanning confocal system with microlensing (CSU-W1 SoRa, Nikon) controlled by NIS elements (Nikon) software was used for imaging. Excitation wavelengths between 405-640 nm, CFI SR Plan ApoIR 60XC WI objective lens and SoRa lens-switched light path at 1x, 2.8x or 4x were used. SoRa images were deconvolved using the Batch Deconvolution (Nikon) software.

    推荐阅读

    Nature Protocols
    Protocols IO
    Current Protocols
    扫码咨询