| 摘要 |
Disclosed in the present invention is a method for inducing the fusion of a dendritic cell with a tumour cell, in the fusion process, successively adding an amount of polyethylene glycol and collagen to induce cell fusion highly efficiently, wherein polyethylene glycol can make the lipid molecules of the plasma membrane at the contact point between the two cells disperse and recombine, and then the cells fuse due to the mutual affinity between the bilayer membranes at the interface of the two cells and the surface tension between each other. The collagen can retrench the cell membrane and repair the cell membrane after fusion, thereby forming stable fusion cells highly efficiently, so it is suitable for the production of specific biological products such as tumour vaccines and monoclonal antibodies etc. |
| 主权项 |
1. A method for inducing fusion of dendritic cell with tumour cell, wherein comprising the following steps:
S1, collecting tumour cells in a centrifuge tube A, collecting dendritic cells in a centrifuge tube B, respectively centrifuging the centrifuge tube A and the centrifuge tube B for 10 minutes at 1500 rpm at room temperature, and counting the cells in the centrifuge tube A and the centrifuge tube B respectively after re-suspending the cells therein with phosphate buffer; S2, adding the tumour cells in the centrifuge tube A and the dendritic cells in the centrifuge tube B into a centrifuge tube C according to a quantity proportion of the tumour cells to the dendritic cells of 1 to 2-5 while controlling a total number of the cells to range from 1×107 to 5 ×107, mixing the cells by whirling, centrifuging the centrifuge tube C for 10 minutes at 1500 rpm at room temperature, removing the supernatant, and placing the centrifuge tube C in a water bath of 40° C. for 3-5 minutes; S3, placing polyethylene glycol with a molecular weight from 1500 to 6000 into the water bath of 40° C. for 2 minutes, adding 200 μl-1000 μl of the polyethylene glycol into the centrifuge tube C within one minute, mixing the cells, and placing the centrifuge tube C in the water bath of 40° C. for 3-5 minutes; S4, first adding 1ml of phosphate buffer into the centrifuge tube C within one minute to stop reacting, then adding and mixing 30 ml-40 ml of the phosphate buffer in the centrifuge tube C within 3-5 minutes; centrifuging the centrifuge tube C for 10 minutes at 1500 rpm at room temperature, removing the supernatant, adding and mixing 30 ml-40 ml of the phosphate buffer in the centrifuge tube C; centrifuging the centrifuge tube C for 10 minutes at 1500 rpm at room temperature, removing the supernatant, and adding 200 μl-800 μl of the phosphate buffer into the centrifuge tube C to re-suspend the cells; S5, adding 2 μl-8 μl of collagen into the centrifuge tube C, and placing the centrifuge tube C in a water bath of 37° C. for 30-50 minutes; S6, adding and mixing 30 ml of the phosphate buffer in the centrifuge tube C, centrifuging the centrifuge tube C for 10 minutes at 1500 rpm at room temperature, removing the supernatant, adding 1640 complete culture medium into the centrifuge tube C and re-suspending the cells to obtain fusion cells. |
