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Protein C activation by recombinant thrombomodulin in plasma.

作者信息

Edano T, Komine N, Yoshizaki H, Ohkuchi M

机构信息

Tokyo Research Laboratories, Kowa Co., Ltd., Japan.

出版信息

Biol Pharm Bull. 1998 Feb;21(2):177-9. doi: 10.1248/bpb.21.177.

Abstract

Recombinant glycosaminoglycan-modified urinary thrombomodulin (GAG-UTM), which partially improved the amino acid sequence of human urinary thrombomodulin (UTM), was expressed in C127 cells. GAG-UTM accelerates protein C activation by thrombin and also thrombin inhibition by antithrombin III (ATIII) in the buffer system. Both accelerating activities of GAG-UTM are more potent than those of unmodified recombinant UTM (r-UTM) without a GAG chain. As ATIII in plasma also inhibits protein C activation by a thrombin-thrombomodulin complex, we studied whether GAG-UTM accelerates protein C activation in plasma. GAG-UTM suppressed the generation of thrombin in activating plasma protein C stronger than r-UTM. By Western blot analysis using anti-protein C antibody, activated protein C was generated by GAG-UTM more than by r-UTM. From these results, the acceleration of activated protein C formation by GAG-UTM was confirmed in plasma too.

摘要

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