Cell killing efficacy detection method and application thereof
A detection method and cell technology, applied in measuring devices, instruments, fluorescence/phosphorescence, etc., can solve problems such as inability to collect cell images, subjective errors of operators and analysts, difficulty in widespread use of flow cytometry, etc.
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Embodiment 1
[0080]This embodiment provides a method for detecting cell killing efficacy, and the specific steps are as follows:
[0081](1) Target cell labeling:
[0082]Cultivate and collect the target cells, add the fluorescent dye CFSE (purchased from Biolegend, USA) to the target cells, incubate, label, and prepare the labeled target cells into a cell solution;
[0083](2) Prepare effector cells:
[0084]Prepare effector cells into cell solution;
[0085](3) Co-cultivation of effective target cells:
[0086]Add target cells and effector cells to the culture dish at the same time, set the effect-to-target ratio to 1:1, take samples after incubation and co-cultivation, add Hoechst33342 (purchased from Thermofisher, USA) and PI dye (purchased from Sigma, USA), and stain;
[0087](4) Add the cells obtained in step (3) to the hemocytometer;
[0088](5) Place the loaded hemocytometer on the sample stage of the detection instrument, and capture the bright field channel, FL1 channel (matching fluorescent dye Hoechst33342)...
Embodiment 2
[0111]This embodiment provides a method for detecting cell killing efficacy, and the specific steps are as follows:
[0112](1) Target cell labeling:
[0113]Cultivate and collect the target cells, add the fluorescent dye CFSE (purchased from Biolegend, USA) to the target cells, incubate, label, and prepare the labeled target cells into a cell solution;
[0114](2) Prepare effector cells:
[0115]Prepare effector cells into cell solution;
[0116](3) Carry out cell co-culture:
[0117]Add target cells and effector cells (as the experimental group) to the culture dish at the same time, set the effect-to-target ratio to 1:1, take a sample after the incubation and co-cultivation, add Hoechst 33342 (purchased from Thermofisher, USA) and PI dye (purchased from Sigma, USA), dyeing;
[0118]Prepare control cells at the same time: add only target cells and culture medium to the culture dish as the target cell control group, and add only the effector cells and culture medium to the other culture dishes as the ef...
Embodiment 3
[0138]Compared with Example 2, in this example, different effective-to-target ratios (E:T) are also set as the experimental group to determine the killing efficacy of cells under different effective-to-target ratios.
[0139]Set the working concentration of effector cells to 1×106 / mL, 3×106 / mL, 6×106For different concentrations of / mL, the corresponding effect-to-target ratios are 1:1, 3:1 and 6:1.
[0140]The resulting overlay image is asFigure 5 As shown, different cells in the figure show different colors. When the effective target is relatively low, the number of live target cells is larger; when the effective target is relatively high, the dead target cells account for the majority. This result further illustrates that when the effective target is relatively high, the effector cells have better killing effect.
[0141]In summary, the method provided by the present invention is relatively intuitive, and can directly obtain visualized cell fluorescence images, obtain different states of c...
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