Human angioma rat animal model and its configuration method
A technology of animal models and construction methods, applied in teaching models, educational tools, instruments, etc., can solve the problems of large differences in hemangiomas
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Embodiment 1
[0032] 1. Isolation and culture of human hemangioma endothelial cells
[0033] Human cavernous hemangioma endothelial cells were isolated using existing methods (see Lou J., Ythier A., Burger D. et al. Modulation of soluble and membrane-bound TNF-induced phenotypic and functional changes of human brain microvascular endothelial cells by recombinant TNF binding protein I. J Neuroimmunology 1997, 77: 107-115.). Briefly, human cavernous hemangioma tissue was cut into 1-2 mm 3Then digested with 0.2% type I collagenase at 37°C for 15 minutes, and then added 0.1% trypsin / 0.1% EDTA solution to continue digestion for 5 minutes. Pass the digested tissue suspension through a 100-mesh copper mesh, collect the liquid, and centrifuge and wash twice with DMEM. The cells were mixed with 2ml of fetal bovine serum (Hyclone Company), and allowed to stand for 2 minutes, and human hemangioma endothelial cell culture medium (containing 20% fetal bovine serum, 100 μg / ml ECGS, 40 U / ml heparin,...
Embodiment 2
[0046] Repeat embodiment 1, its difference is only: get 5 * 10 5 Individual hemangioma endothelial cells with 1 x 10 5 The human osteosarcoma cell line HOS cells are co-inoculated; the immunodeficiency experimental animals are SCID mice.
Embodiment 3
[0048] Repeat embodiment 1, its difference is only: get 1 * 10 6 The personal liver cancer cell line HepG2 was suspended in 1ml DMEM and crushed by ultrasonication. The ultrasonic condition was 10 seconds each time with an interval of 30 seconds. The supernatant was collected by centrifugation at 10000g for 10 minutes, and then 1×10 7 The human hemangioma endothelial cells are mixed with the supernatant and co-inoculated; the immunodeficiency experimental animals are SCID mice.
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