Anti-thrombosis effect of LRRFIP1 shRNA lentivirus in a mouse model of deep vein thrombosis
| Autor: | Siyu Wu, Ai-min Wang, Quanyin Du, Ziming Wang, Yu Wang, Xiang Yin |
|---|---|
| Rok vydání: | 2013 |
| Předmět: |
Male
medicine.medical_specialty medicine.drug_class Deep vein Genetic Vectors Low molecular weight heparin Pharmacology Transfection Inferior vena cava Fibrin Fibrinogen Degradation Products Small hairpin RNA Mice Animals Medicine cardiovascular diseases RNA Small Interfering Thrombus Cells Cultured Venous Thrombosis Mice Inbred ICR business.industry Lentivirus Anticoagulants Hematology Heparin Low-Molecular-Weight Phosphoproteins medicine.disease Thrombosis Surgery Disease Models Animal P-Selectin Venous thrombosis medicine.anatomical_structure medicine.vein RNA Interference business Ligation |
| Zdroj: | Thrombosis Research. 132:127-131 |
| ISSN: | 0049-3848 |
| DOI: | 10.1016/j.thromres.2013.05.013 |
| Popis: | Introduction Deep vein thrombosis (DVT) is one of the common complications of orthopedic surgery. Low molecular weight heparin (LMWH) is a usually used agent for DVT, but it would increase the risk of bleeding. LRRFIP1 has been shown to play an important role in the formation of thrombosis. Therefore, we investigated the effect of LRRFIP1 shRNA lentivirus on DVT in mice. Materials and Methods Lentiviral Vectors carrying LRRFIP1 shRNA were constructed and transfected into cultured mouse bone marrow cells (BMCs). Male ICR mice were irradiated with a single dose of 9.5 Gy and then were injected with different agents through the tail vein. Stasis venous thrombosis was induced by inferior vena cava (IVC) ligation. Mice were sacrificed on the 1st, 3rd and 7th day post operation and the thrombi were removed, blotted the excess blood on it with filter paper and immediately weighed. P-selectin and d-Dimer were determined by enzyme-linked immunosorbent assay (ELISA). Results LRRFIP1 shRNA significantly suppressed the expression of LRRFIP1 in the thrombi. In contrast, low molecular weight heparin (LMWH) and negative shRNA exhibited little effect on the expression of LRRFIP1. LRRFIP1 shRNA, LMWH and negative shRNA inhibited the thrombus formation in vivo significantly. The plasma P-selectin and d-Dimer levels were significantly increased after IVC ligation. LRRFIP1 shRNA significantly decreased the plasma P-selectin and d-Dimer levels. However, LMWH and negative shRNA showed little effects on the levels of plasma P-selectin and d-Dimer. Conclusion LRRFIP1 shRNA might represent a promising prevention strategy for DVT. |
| Databáze: | OpenAIRE |
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