Highly aggressive human acute B lymphocytic leukemia cell strain with add(11)(q23) chromosome abnormality
A technology of leukemia cells and B lymphocytes, which is applied in the field of human acute B lymphocytic leukemia and highly aggressive human acute B lymphocytic leukemia cell lines, can solve problems such as abnormal chromosome structure, and achieve important biological significance and practical value. Highly tumorigenic, highly invasive effect
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Embodiment 1
[0061] Isolation and strain establishment of embodiment 1CHH-1 cell strain
[0062] The cells involved in the present invention are all suspended and cultured in the RPMI1640 cell culture medium containing 10% fetal bovine serum (FBS); the culture temperature is 37° C., and the gas environment is 5% CO 2 / 95% air, humidity is saturated humidity. ; Passage at a ratio of 1:2.
[0063] 1) Isolation and inoculation of B-lineage precursor cells from the patient's bone marrow
[0064] ①Put 10ml of the patient's bone marrow fluid obtained by Guchuan into a sterile sodium heparin anticoagulant tube, and separate the patient's bone marrow mononuclear cells with Ficoll human lymphocyte separation medium;
[0065] ②Press 2×10 6 / ml cell density Inoculate isolated bone marrow mononuclear cells into 24-well cell culture plates, add RPMI1640 medium containing 50ng / ml recombinant human IL-3, 50ng / ml recombinant human SCF and 20% FBS, and place at 37°C , the gas environment is 5% CO 2 / 9...
Embodiment 2
[0075] Example 2 CHH-1 cell line mouse tumorigenic experiment and invasion experiment
[0076] 1) NOD / SCID mouse tumorigenic experiment
[0077] ①The CHH-1 cells in the logarithmic growth phase were divided into 5×10 6 / 200μl / only inoculated subcutaneously in NOD / SCID mice;
[0078] ②Observe the tumorigenicity of the tumor cells at the inoculation site daily, measure the longest diameter and shortest diameter of the tumor mass after tumor formation, and calculate the volume of the tumor mass;
[0079] ③16 days after inoculation, a rice-grain-sized lump could be touched at the subcutaneous cell injection site of the mouse, and a lump protruding from the skin could be observed with the naked eye on the 28th day, and the mouse was sacrificed on the 28th day, and the tumor was separated to make tissue sections for H-E staining and immunohistochemical staining , and after the tumor cells were separated, the karyotype analysis and Ig gene rearrangement detection were performed aga...
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