An ectopic ossification arthritis animal model and a construction method and application thereof
By emulsifying chondroitin sulfate proteoglycan Versican peptide VG191-115 with chicken type II collagen and then immunizing animals with the mixture, followed by subcutaneous injection and intraperitoneal injection of Curdlan, a highly efficient heterotopic ossifying arthritis model was successfully constructed. This solved the problem of the difficulty in constructing existing models and realized a high-success-rate platform for simulating and researching heterotopic ossifying arthritis.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- NANJING UNIV OF TRADITIONAL CHINESE MEDICINE
- Filing Date
- 2025-07-22
- Publication Date
- 2026-06-09
AI Technical Summary
Existing animal models of heterotopic ossification of arthritis are difficult to construct, involve complex and costly material acquisition, and cannot effectively simulate the pathogenesis of human osteoarthritis, thus limiting related research and drug development.
Animals were immunized with a mixture of chondroitin sulfate proteoglycan peptide VG191-115 and chicken type II collagen to form a water-in-oil emulsion, which was then injected subcutaneously. This was combined with intraperitoneal injection of fungal polysaccharide Curdlan to induce symptoms of heterotopic ossifying arthritis.
The constructed C2V7 model has a high success rate, short processing time, and readily available modeling materials. It can simulate the pathogenesis of human heterotopic ossifying arthritis, provide a stable research platform, reflect pathological characteristics, and support pathological mechanisms and targeted therapies.
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Figure CN120837623B_ABST
Abstract
Claims
1. A method for constructing an animal model of heterotopic ossifying arthritis, characterized in that, This includes the peptide VG1 from chondroitin sulfate proteoglycan. 91-115 As an antigen, it was mixed with type II collagen and emulsified before being used to immunize animals; the polypeptide VG1 91 -115 The amino acid sequence is shown in SEQ ID NO: 1; the animal is a BALB / c mouse or a DBA / 1 mouse.
2. The method according to claim 1, characterized in that, include: Synthetic peptide VG1 91-115 ; The polypeptide VG1 91 -115 The mixture was mixed with chicken type II collagen solution, then emulsified with complete Freund's adjuvant to form a water-in-oil emulsion; the emulsion was then subcutaneously injected into the tail of mice.
3. The method according to claim 2, characterized in that, include: Chemically synthesized peptide VG1 91-115 VG1 91-115 Mix the emulsion with 2 mg / mL chicken type II collagen solution and 4 mg / mL complete Freund's adjuvant at a 1:1 ratio. Place the mixture in ice water and homogenize at 8000 rpm for 2 minutes, pause for 2 minutes, and repeat the homogenization process 15-20 times to form an emulsion that does not disperse when dropped into water. Administer 100 μL of the emulsion per mouse to BALB / c or DBA / 1 mice by inserting a needle 2 cm from the base of the tail until the needle tip is 0.5 cm from the tail base. Inject the emulsion intraperitoneally with 200 μL of 15 mg / mL fungal polysaccharide Curdlan on the day of injection and again 7 days later.
4. The method according to claim 1, characterized in that, The fungal polysaccharide Curdlan was injected intraperitoneally into the animals on the day of immunization and one week later.
5. The use of the animal model of heterotopic ossifying arthritis obtained by the method of any one of claims 1-4 in screening or identifying compounds for treating or alleviating heterotopic ossifying arthritis, or in studying the disease mechanism of heterotopic ossifying arthritis.
6. A method for screening candidate drugs or therapeutic agents to relieve or treat heterotopic ossifying arthritis, characterized in that, include: An animal model of heterotopic ossifying arthritis is obtained by the method according to any one of claims 1-4; the candidate drug or therapeutic agent is administered to the animal model, and if the arthritis symptoms of the animal model are relieved, the candidate drug or therapeutic agent is used as an active ingredient for relieving or treating heterotopic ossifying arthritis.