Immunoliposome based on Nrdp1 gene RNAi and miR-494 and application thereof
A technology of mir-494 and immunoliposome, which is applied in the field of genetic engineering, can solve the problems of lack of therapeutic drugs, inflammatory reactions that do not cause clinicians, damage, etc., and achieve the effect of inhibiting the initiation process of inflammation, good application prospects, and increasing content
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Embodiment 1
[0053] Example 1 Preparation of immunoliposome (RNAi of Anti-F4 / 80-Lip-miR-494 / Nrdp1 gene) based on RNAi of miR-494 / Nrdp1 gene
[0054] 1. Preparation and detection of RNAi recombinant eukaryotic expression vector of miR-494 / Nrdp1 gene
[0055] (1) Preparation of RNAi recombinant eukaryotic expression vector of miR-494 / Nrdp1 gene
[0056] The nucleotide sequence shown as SEQ ID NO:1 was synthesized. Two corresponding inverted repeat sequences were designed: as shown in SEQ ID NO: 2 and SEQ ID NO: 3, they were used as primers to clone and obtain the target DNA fragment.
[0057] The above DNA strands were annealed and ligated with the plasmid vector pGenesil-1. T4 ligase ligated the annealed nucleotide to pGenesil-1 and transformed it into Escherichia coli DH5α, screened positive clones with LB plates containing ampicillin, extracted plasmids for identification, and inserted NotI and XbaI sites of pGenesil-1 The positive cloning plasmid of the RNAi gene of the miR-494 / Nrdp1 ...
Embodiment 2
[0073] Anti-inflammatory effect research of embodiment 2 immunoliposome
[0074] 1. Detection of NRDP1 in microglial cells after red blood cell lysate treatment,
[0075]Add 10 μl of erythrocyte lysate to 0.1 mg of immunoliposome-incubated microglia or control microglia, at 37°C for 24 hours, and detect the expression of NRDP1 in microglial cells stimulated by erythrocyte lysate by WB method. Research results such as image 3 As shown, immunoliposome-incubated microglia expressed less NRDP1 than control microglia.
[0076] 2. Detection of inflammatory factors in microglial cells after red blood cell lysate treatment,
[0077] Add 10 μl of erythrocyte lysate to 0.1 mg of immunoliposome-incubated microglia or control microglia, 37°C, 24h, use ELISA to detect that erythrocyte lysate stimulates microglia to secrete IL-8 and TNF- Alpha capabilities. Research results such as Figure 4 As shown, the immunoliposome-incubated microglia secreted less IL-8 and TNF-α than the control...
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