Thromb Haemost 1982; 48(02): 208-210
DOI: 10.1055/s-0038-1657258
Original Article
Schattauer GmbH Stuttgart

A Unique Pathway for the Plasma Elimination of α2-Antiplasmin-Protease Complexes in Mice

S L Gonias
The Departments of Pathology and Biochemistry, Duke University Medical Center, Durham, North Carolina, U.S.A.
,
H E Fuchs
The Departments of Pathology and Biochemistry, Duke University Medical Center, Durham, North Carolina, U.S.A.
,
S V Pizzo
The Departments of Pathology and Biochemistry, Duke University Medical Center, Durham, North Carolina, U.S.A.
› Author Affiliations
Further Information

Publication History

Received 20 April 1982

Accepted 20 August 1982

Publication Date:
13 July 2018 (online)

Summary

Radiolabeled α2-antiplasmin cleared slowly from the circulation of mice. Complex formation with either plasmin or trypsin resulted in a significant increase in the plasma elimination rate of the protease inhibitor. Approximately 20 min and 14 min were required for 50% of the injected α2-antiplasmin-plasmin and α2-antiplasmin-trypsin to clear from the circulation, respectively. Significant competition was observed when radiolabeled α2-antiplasmin-plasmin was cleared in the presence of a large molar excess of unlabeled α2-antiplasmin-plasmin. α1-Antitrypsin-trypsin failed to compete with radiolabeled α2-antiplasmin-plasmin even when present at 2000 fold molar excess. Organ distribution studies localized the major site of α2-antiplasmin-plasmin clearance in the liver. Microscopic autoradiography data suggested that the cell responsible for the clearance pathway was the hepatocyte.

 
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