• 云顶集团3118(中国)

    Isolation of nuclei from frozen human skeletal and cardiac muscle for single nucleus RNA and chromatin assays 

    Dinh H Diep, Sebastian Preissl, James R Hocker

    Published: 2021-12-18 DOI: 10.17504/protocols.io.b2z4qf8w
    AI 解读
    浏览 1760

    Abstract

    This protocol was adapted for the isolation of single nuclei from frozen skeletal and cardiac muscle tissues for molecular characterization with the SNARE-seq2, sci-ATAC-seq, and snRNA-seq assays.

    References:

    (1) Preissl et al (2015). Circulation Research. Doi: 10.1161/CIRCRESAHA.115.306337

    (2) Hocker et al (2021). Science Advances. Doi: 10.1126/sciadv.abf1444

    Steps

    1.

    Section flash-frozen skeletal muscle into aliquots according to desired nuclei yield and store on dry ice or at -80°C .

    Note
    Expect yield of 2000-4000 nuclei per mg of skeletal muscle tissue.

    2.

    Prepare buffers and chill components:

    ABC
    Tissue massMACS bufferNPB buffer
    10-50mg1 mL2 mL
    50-100mg2 mL4 mL
    >100mg3 mL1 mL per 25 mg

    Note: May require further optimization.

    • Prepare buffer fresh on day of nuclei isolation
    • Precool centrifuge to 4°C
    • Precool all buffers at 4°C
    • Place gentleMACS dissociator in cold room / chiller
    • Chill gentleMACS M tubes on ice
    • Chill 5.0 mL Eppendorf tubes on ice
    3.

    Transfer sectioned frozen tissue to gentleMACS M tubes.

    4.

    Add the recommended volume of MACS buffer to gentleMACS M tube.

    Note
    Allow tissue to thaw in MACS buffer for approximately 60 seconds on ice.

    5.

    Homogenize with Miltenyi tissue dissociation protocol: "Protein_01_01" on the gentleMACS instrument in the chiller/cold room.

    6.

    Briefly centrifuge the gentleMACS M tube to pull all the homogenate to the bottom.160x g,4°C

    7.

    Filter homogenate through 30 uM CellTrics filter into 5 mL Eppendorf Tubes.

    8.

    Wash gentleMACS M tube with another 1 mL of MACS buffer and filter the wash.

    9.

    900x g,4°C

    Note
    Use ramp rate: 3/9 acceleration and 3/9 deceleration.

    10.

    Decant and discard the supernatant.

    11.

    Resuspend the pellet with the recommended NPB buffer.

    12.

    Gently rotate the sample in cold room/chiller for 0h 10m 0s .

    Note
    Users should optimize lysis timing for different samples. (i.e., 5 minutes for cardiac tissues).

    13.

    Centrifuge permeabilized nuclei at 900x g,4°C .

    14.

    Decant and discard the supernatant.

    15.

    Resuspend the pellet in 500 uL PBS + RNase In.

    Note
    For SNARE-seq2: immediately fix nuclei by adding (1:1) 500 uL PBS + Rnase In + 1% paraformaldehyde. (Make 1 mL : 937.5 uL PBS+RI + 62.5 uL 16% methanol-free PFA). Incubate on ice for 0h 10m 0s

    16.

    QA/QC : Count the nuclei. Mix 1:1 volume of cellular suspension with a staining solution (ie DAPI). Load 10 uL of mixture onto a Biorad Cell Counter slide then count with a BioRad TC20 Cell Counter. Gate 4 uM-6 uM for nuclei sizes.

    17.

    QA/QC : Check nuclei integrity under fluorescent microscope using DAPI channel. Nuclei should appear distinct , have rounded borders and the majority occurring as singlets .

    Note
    If high clumping is observed: bring total volume to ~1 mL with PBS+0.1%BSA and filter the sample through a 30 uM CellTrics filter. Pellet 900x g,4°C,0h 10m 0s . Then resuspend again in 100 uL PBS + Rnase In.If high debris is observed (low DAPI+): bring volume to ~ 1 mL with PBS+0.1%BSA and pellet: 900x g,4°C,0h 10m 0s . Then resuspend again in 100 uL PBS + RNase In.

    推荐阅读

    Nature Protocols
    Protocols IO
    Current Protocols
    扫码咨询