1. Glycosaminoglycans affect the interaction of human plasma kallikrein with plasminogen, factor XII and inhibitors.
- Author
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Gozzo AJ, Nunes VA, Nader HB, Dietrich CP, Carmona AK, Sampaio MU, Sampaio CA, and Araújo MS
- Subjects
- Animals, Cattle, Complement C1 Inactivator Proteins drug effects, Complement C1 Inhibitor Protein, Cysteine Proteinase Inhibitors pharmacology, Factor XII physiology, Humans, Plasma Kallikrein antagonists & inhibitors, Plasma Kallikrein physiology, Factor XII drug effects, Fibrinolytic Agents pharmacology, Glycosaminoglycans pharmacology, Plasma Kallikrein drug effects, Plasminogen drug effects
- Abstract
Human plasma kallikrein, a serine proteinase, plays a key role in intrinsic blood clotting, in the kallikrein-kinin system, and in fibrinolysis. The proteolytic enzymes involved in these processes are usually controlled by specific inhibitors and may be influenced by several factors including glycosaminoglycans, as recently demonstrated by our group. The aim of the present study was to investigate the effect of glycosaminoglycans (30 to 250 micro/ml) on kallikrein activity on plasminogen and factor XII and on the inhibition of kallikrein by the plasma proteins C1-inhibitor and antithrombin. Almost all available glycosaminoglycans (heparin, heparan sulfate, bovine and tuna dermatan sulfate, chondroitin 4- and 6-sulfates) reduced (1.2 to 3.0 times) the catalytic efficiency of kallikrein (in a nanomolar range) on the hydrolysis of plasminogen (0.3 to 1.8 microM) and increased (1.9 to 7.7 times) the enzyme efficiency in factor XII (0.1 to 10 microM) activation. On the other hand, heparin, heparan sulfate, and bovine and tuna dermatan sulfate improved (1.2 to 3.4 times) kallikrein inhibition by antithrombin (1.4 microM), while chondroitin 4- and 6-sulfates reduced it (1.3 times). Heparin and heparan sulfate increased (1.4 times) the enzyme inhibition by the C1-inhibitor (150 nM).
- Published
- 2003
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