TAP-SSL5 FUNCTIONS AS AN ANTICOAGULANT AND ANTI-INFLAMMATORY PROTEIN TO INHIBIT THROMBOSIS IN RAT AND ATTENUATE ATHEROSCLEROSIS IN APOE-KNOCKOUT MOUSE. (8th October 2012)
- Record Type:
- Journal Article
- Title:
- TAP-SSL5 FUNCTIONS AS AN ANTICOAGULANT AND ANTI-INFLAMMATORY PROTEIN TO INHIBIT THROMBOSIS IN RAT AND ATTENUATE ATHEROSCLEROSIS IN APOE-KNOCKOUT MOUSE. (8th October 2012)
- Main Title:
- TAP-SSL5 FUNCTIONS AS AN ANTICOAGULANT AND ANTI-INFLAMMATORY PROTEIN TO INHIBIT THROMBOSIS IN RAT AND ATTENUATE ATHEROSCLEROSIS IN APOE-KNOCKOUT MOUSE
- Authors:
- Qu, Xiaolong
Fang, Zhaofei
Li, Min
Huang, Dexing
Hu, Houyuan - Abstract:
- Abstract : Objectives: This study aims to inhibit the inflammatory response and thrombosis in atherosclerotic lesions, by using the staphylococcal superantigen-like protein-5 (SSL5) to inhibit neutrophil activation, and tick anticoagulant peptide (TAP) to inhibit factor Xa (FXa) activation. To achieve this, we made a novel fusion protein TAP-SSL5 and tesed its dual anticoagulant and anti-inflammatory properties.t Methods: We put six flexible amino acids sequence between TAP and SSL5 genes as a linker. The polycistronic fragment was constructed and then subcloned into a pET22b(+) expression vector. The binding ability of TAP-SSL5 to P-selectin glycoprotein ligand-1(PSGL-1) on leukocytes was verified by flow cytometry. The binding of TAP-SSL5 to PSGL-1 inhibited the adhesion of leukocytes to P-selectin-coated surface. FXa activity was determined by chromogenic substrate assay. Results: We have observed that TAP-SSL5 inhibited FXa activity in a concentration-dependent manner and TAP-SSL5 reduced ferric chloride-induced thrombosis in the inferior vena cava of rat. In a high-fat diet induced atherosclerotic model by using ApoE-knockout (ApoE −/− ) mouse, male ApoE −/− mice were grouped to receive intraperitoneal treatment with either TAP-SSL5 (3 mg/kg/day), SSL5 (2 mg/kg/day) or vehicle separately. After 12 weeks of the respective treatment, we have observed that TAP-SSL5 reduced the atherosclerotic plague formation by 48% compared to controls. We also found TAP-SSL5 couldAbstract : Objectives: This study aims to inhibit the inflammatory response and thrombosis in atherosclerotic lesions, by using the staphylococcal superantigen-like protein-5 (SSL5) to inhibit neutrophil activation, and tick anticoagulant peptide (TAP) to inhibit factor Xa (FXa) activation. To achieve this, we made a novel fusion protein TAP-SSL5 and tesed its dual anticoagulant and anti-inflammatory properties.t Methods: We put six flexible amino acids sequence between TAP and SSL5 genes as a linker. The polycistronic fragment was constructed and then subcloned into a pET22b(+) expression vector. The binding ability of TAP-SSL5 to P-selectin glycoprotein ligand-1(PSGL-1) on leukocytes was verified by flow cytometry. The binding of TAP-SSL5 to PSGL-1 inhibited the adhesion of leukocytes to P-selectin-coated surface. FXa activity was determined by chromogenic substrate assay. Results: We have observed that TAP-SSL5 inhibited FXa activity in a concentration-dependent manner and TAP-SSL5 reduced ferric chloride-induced thrombosis in the inferior vena cava of rat. In a high-fat diet induced atherosclerotic model by using ApoE-knockout (ApoE −/− ) mouse, male ApoE −/− mice were grouped to receive intraperitoneal treatment with either TAP-SSL5 (3 mg/kg/day), SSL5 (2 mg/kg/day) or vehicle separately. After 12 weeks of the respective treatment, we have observed that TAP-SSL5 reduced the atherosclerotic plague formation by 48% compared to controls. We also found TAP-SSL5 could down-regulate several kinds of inflammatory cytokine expressions in vascular wall which were detected by mouse inflammatory antibody array. Conclusions: TAP-SSL5 fusion protein has promising anti-inflammatory and anti-thrombosis properties, and it acquires the potential for the prevention of atherosclerotic lesion and thrombus formation. … (more)
- Is Part Of:
- Heart. Volume 98(2012)Supplement 2
- Journal:
- Heart
- Issue:
- Volume 98(2012)Supplement 2
- Issue Display:
- Volume 98, Issue 2 (2012)
- Year:
- 2012
- Volume:
- 98
- Issue:
- 2
- Issue Sort Value:
- 2012-0098-0002-0000
- Page Start:
- E130
- Page End:
- E131
- Publication Date:
- 2012-10-08
- Subjects:
- Heart -- Diseases -- Treatment -- Periodicals
Cardiology -- Periodicals
616.12 - Journal URLs:
- http://www.bmj.com/archive ↗
http://heart.bmj.com ↗
http://www.heartjnl.com ↗ - DOI:
- 10.1136/heartjnl-2012-302920c.9 ↗
- Languages:
- English
- ISSNs:
- 1355-6037
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23738.xml