MiR-29 sponge, nucleic acid construct containing same and applications of miR-29 sponge
A technology of nucleic acid constructs and sponges, applied in the field of biomedicine, can solve problems such as application limitations, inability to meet the needs of metabolism, and individual differences in patients, so as to achieve the effects of improving survival rate, inhibiting secretion, and reducing the incidence of disease
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Embodiment 1
[0035] Example 1 Effect of miR-29sponge on the onset of type 1 diabetes in NOD mice.
[0036] Experimental animals: 8-9-week-old female NOD mice and feed, provided by Beijing Huafukang Biotechnology Co., Ltd., license number: SCXK (Beijing) 2019-0008. Animals were housed in random cages, with free access to food and water.
[0037] Experimental drug: HBLV-mmu-miR-29 sponge was prepared and purified by Hanheng Technology (Shanghai) Co., Ltd. The negative control was HBLV-mmu-GFP NC, which was purchased from Hanheng Technology Company. Among them, HBLV-mmu-miR-29 sponge The lentiviral expression vector used was pHBLV-U6-MCS-CMV-ZsGreen; the competent cell was Escherichia coli strain DH5α; resistance: Amp.
[0038] Experimental steps:
[0039] 1) 8-9 week-old female NOD mice entered the Experimental Animal Center of Nanjing Medical University, raised in a clean environment, temperature (21±2)℃, humidity (35±2)%, 12h:12h day and night lighting, free to eat Drinking water, drink...
Embodiment 2
[0056] Example 2 The effect of miR-29 sponge on the levels of pro-inflammatory and anti-inflammatory cytokines in the serum of NOD mice.
[0057] Take 50ul of the collected serum sample and add it to the flow tube, add 50ul of the inflammatory factor magnetic bead mixture in the CBA kit (BD company, USA), incubate at room temperature for 1 hour, then add 50ul of the PE detection kit (BD company in the United States) mixture, and keep at room temperature Incubate for 1 hour. After the incubation, add 1ml of cleaning solution and centrifuge at room temperature 200g for 5min, discard the supernatant, resuspend with 300ul cleaning solution, and detect on the flow cytometer.
[0058] The results are shown in Figure 8. It was found that compared with the GFP control group, the miR-29 sponge treatment group could significantly reduce the levels of inflammatory cytokines TNF-α, IL-6 and MCP-1 in the serum of NOD mice. Figure A The content distribution of TNF-α, IL-6, IL-1β and MCP-1 ...
Embodiment 3
[0059] Example 3 Effect of miR-29 sponge on circulating monocytes of NOD mice.
[0060] The number of monocytes in the circulation of the mice in Example 1 was analyzed by flow cytometry, and the difference between the GFP group and the miR-29 sponge experimental group was compared. Specific steps are as follows:
[0061] Add 20ul of 6250U / ml heparin sodium to 80ul of peripheral blood of the mouse, mix well, let stand at 37°C for 1h, and absorb plasma and buffy coat. Plasma is used for CBA and other detections. Add 3 times the volume of erythrocyte lysate to the middle white blood cell layer, room temperature for 5 minutes, mix well, after lysing, wash with PBS and mark the corresponding flow cytometry antibody F4 / 80, MHCII (both purchased from eBioscience, Inc., USA) ). Incubate at room temperature in the dark for 15 minutes, wash with PBS once, and discard the supernatant. Finally, resuspend in 300ul PBS to make mononuclear cell suspension. Take 1×10 6 The cells were co...
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