Application of nuclear factor chiB inhibition protein 1 combined with A20 to preparation of medicine for treating fatty livers and related diseases
A technology to inhibit protein and nuclear factor, applied in gene therapy, metabolic disease, drug combination, etc., to achieve high safety effect
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Embodiment 1
[0097] [Example 1] Effect of ABIN1 overexpression on fat accumulation in L02 cells
[0098] Construct a lentiviral expression vector that overexpresses ABIN1, transfect HEK-293T cells, package the lentivirus, infect L02 cells to construct a stable cell line that overexpresses ABIN1, and overexpress the empty vector as a control (Con), and detect stable cells by Western blot Whether the strain expresses ABIN1.
[0099] After the detection was completed, the cells were divided into 4 groups, namely: L02 empty control group, ABIN1 overexpressed L02 stable cell line control group, L02-empty experimental group, ABIN1 overexpressed L02 stable cell line experimental group. After the cells adhered to the wall and the cells were cultured to 50% healing, palmitate (PA) and oleic acid (OA) (PA 0.2mM+OA 0.4mM) were added to the two experimental groups for stimulation, and the same amount was added to the control group. After 12 hours, the cell samples of each group were collected and sta...
Embodiment 2
[0101] [Example 2] Effect of overexpression of ABIN1 on fat accumulation in mouse primary liver cells
[0102] Construct a lentiviral expression vector that overexpresses ABIN1, transfect HEK-293T cells, package the lentivirus, and infect mouse primary liver cells to construct a cell model that overexpresses ABIN1, and overexpress the empty vector as a control (Con). Blot was used to detect whether the cells in the ABIN1-infected group overexpressed ABIN1.
[0103] After the detection was completed, the cells were divided into 4 groups, namely: no-load control group, ABIN1 overexpressed cell control group, L02-no-load experimental group, and ABIN1 overexpressed cell experimental group. After the cells adhered to the wall and the cells were plated to a degree of 50% healing, palmitate (PA) and oleic acid (OA) (PA 0.2mM+OA0.4mM) were added to the two experimental groups for stimulation, and the same amount was added to the control group. After 12 hours, the cell samples of each...
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