A kind of target cell for testing car-t cell killing effect and its preparation method and application
A technology of target cells, CCC-3T3, is applied in the field of target cells and its preparation for testing the killing effect of CAR-T cells. The effects of heterosexual killing, sensitive killing signal, and low killing background
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[0031] The present invention also provides a method for preparing the target cell CCC-3T3, comprising the following steps: 1) connecting the Caveolin-1 gene and the caspase-3 gene with a connecting peptide to obtain the fusion protein gene of Caveolin-1 and caspase-3; 2. ) transfer the fusion protein gene of Caveolin-1 and caspase-3 into mouse fibroblast-like cells by lentiviral transfection method to obtain CC-3T3 cells expressing the fusion protein; 3) transfer CAR-T by lentiviral transfection method The cell target antigen gene was transferred into CC-3T3 cells to obtain target cells CCC-3T3.
[0032] In the present invention, the fusion protein gene of Caveolin-1 and caspase-3 is obtained by linking Caveolin-1 gene and caspase-3 gene with connecting peptide; Methods: Caveolin-1 gene, connecting peptide gene and caspase-3 gene connected in sequence were synthesized as a fusion gene.
[0033]In the present invention, after the fusion protein gene of Caveolin-1 and caspase-3...
Embodiment 1
[0045] 1. Construction of lentiviral transfection experiment
[0046] (1) Recovery culture HEK-293T ( CRL-11268 TM ), pass on 1-2 generations. The day before the transfection, the cells were collected and counted, diluted to 5×105cells / mL, spread 20mL to a 15cm culture dish, and placed in a 37°C, 5% CO2 incubator for culture.
[0047] (2) On the day of transfection, take two 15mL centrifuge tubes and add plasmids and reagents according to Table 1.
[0048] Table 1 Reagents for transfection
[0049]
[0050]
[0051] (3) Stand at room temperature for 5 minutes.
[0052] (4) Transfer the liquid from tube A to tube B and mix well.
[0053] (5) Stand still at room temperature for 20 minutes.
[0054] (6) Cell replacement: use a pipette to suck out the culture medium, add 10mL DMEM, shake gently, and then suck it up. Add 18mL DMEM to the Petri dish, shake it gently and place it at 37°C with 5% CO2 for culture.
[0055] (7) Pipette the mixture of tubes A and B with a ...
Embodiment 2
[0096] The CAR-T cell target antigen gene was replaced with the CD20 gene, and the rest of the steps were the same as in Example 1.
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