The function of irf9 in restenosis after stent and endarterectomy and the application of its inhibitor
A technology for restenosis and vascular stenosis, applied in the application field of function and its inhibitors, can solve the problems of high incidence and affect the treatment effect, and achieve the effect of promoting restenosis
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Embodiment 1
[0031] Example 1 Mouse Vascular Injury Model (VI) Obtained
[0032] 1. Grouping of experimental animals: WT and IRF9-KO mice aged 8-10 weeks and weighing 24-27g were used and divided into four groups: WT vascular injury group; WT sham operation group; IRF9-KO vascular injury group; IRF9 - KO sham operation group, 60 mice in each group. Twenty mice in each group were sacrificed 7 days, 14 days, and 28 days after the operation, and blood vessels in the injured segment were collected for analysis.
[0033] 2. Operation procedure of mouse vascular injury model:
[0034] 1) Accurately weigh the body weight (g) of the mouse in dynamic mode with an electronic balance, accurately prepare 3% pentobarbital sodium solution with double distilled water, shake gently to dissolve it fully, and use 80mg / kg body weight dose to calculate Accurately extract the corresponding volume of pentobarbital sodium solution with a 1mL syringe, and intraperitoneally inject the anesthetized mouse. After t...
Embodiment 2
[0039] Example 2 Determination of Intimal Neogenesis in Vascular Injury Model (VI) Mice
[0040] 1. Mice Harvesting
[0041] 1) Anesthetize the mouse, cut the heart and let the blood out.
[0042] 2) Cut the carotid artery from the proximal bifurcation of the carotid artery, take 0.5-0.6cm long, and keep the external carotid artery knot.
[0043] 3) Put the carotid artery in PBS, and gently drain the residual blood in the lumen with micro forceps.
[0044] 4) Put the blood vessel into a 1.5mL EP tube filled with 1mL 4% paraformaldehyde for fixation.
[0045] 2. Pathological detection
[0046] 2.1 Preparation of paraffin specimen slices
[0047] Paraffin specimen sections are prepared by professional pathological staff in the laboratory. The main operating procedures include trimming the heart → processing the embedding frame → washing with running water → dehydrating → transparent → dipping in wax → embedding → sectioning (3 μm) → spreading → drying or baking Backup.
[...
Embodiment 3
[0055] Example 3 Detection of proliferation level of blood vessel wall cells
[0056] The expressions of proliferating cell nuclear antigen (PCNA) and cell cycle protein (Cyclin D1) were detected by immunofluorescence staining. Required primary antibody information: PCNA (#2586; 1:100; mouse; Cell Signaling Technology), cyclin D1 (#2978; 1:25; rabbit; Cell Signaling Technology); required secondary antibody information: Alexa Fluor 568-conjugated goat anti-rabbit IgG (A11011; Invitrogen, Carlsbad, CA), Alexa Fluor 568-conjugated goat anti-mouse IgG (A11004; Invitrogen, Carlsbad, 150 d, CA).
[0057] The main steps are:
[0058] 1) Baked slices: put the paraffin slices in the oven for more than 30 minutes.
[0059] 2) Dewaxing: Xylene 5min×3.
[0060] 3) Hydration: 100% ethanol 5min×2; 95% ethanol 5min; 70% ethanol 5min; ddH 2 O dipping for 5min×2.
[0061] 4) Citrate tissue antigen repair (high pressure repair): Take a certain amount of pH6.0 citrate antigen repair working...
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