Thromb Haemost 2001; 85(02): 349-355
DOI: 10.1055/s-0037-1615691
Review Article
Schattauer GmbH

Purification of Proplatelet Formation (PPF) Stimulating Factor: Thrombin/Antithrombin III Complex Stimulates PPF of Megakaryocytes In Vitro and Platelet Production In Vivo

Yoji Ishida
1   Division of Hematology, IIIrd Department of Internal Medicine, Iwate Medical University School of Medicine, Morioka, Iwate, Japan
,
Kazuo Yano
2   Bio-Science Laboratory, Life Science Research Laboratories, Asahi Chemical Industry, Fuji, Shizuoka, Japan
,
Toshiharu Ito
1   Division of Hematology, IIIrd Department of Internal Medicine, Iwate Medical University School of Medicine, Morioka, Iwate, Japan
,
Hiroki Shigematus
2   Bio-Science Laboratory, Life Science Research Laboratories, Asahi Chemical Industry, Fuji, Shizuoka, Japan
,
Kohsuke Sasaki
3   Department of Pathology, Yamaguchi University School of Medicine, Ube, Yamaguchi, Japan
,
Shuhei Kondo
2   Bio-Science Laboratory, Life Science Research Laboratories, Asahi Chemical Industry, Fuji, Shizuoka, Japan
,
Shin-Ichiro Kuriya
1   Division of Hematology, IIIrd Department of Internal Medicine, Iwate Medical University School of Medicine, Morioka, Iwate, Japan
› Author Affiliations
Further Information

Publication History

Received 12 April 2000

Accepted after resubmission 18 September 2000

Publication Date:
08 December 2017 (online)

Summary

In this study, the protein which stimulates proplatelet formation (PPF) of megakaryocytes was purified from normal human plasma using 7 steps procedures. Two different protease inhibitors were identified based on their amino acid sequences, i.e. antithrombin III (AT III) and C1 inhibitor. They were included in high density lipoprotein (HDL). HDL was necessary for AT III to be active in PPF in vitro. The biological effects of the AT III /HDL or thrombin-AT III (TAT)/HDL were studied in vitro. PPF of murine megakaryocytes was stimulated by negative control (BSA) (1.8 ± 0.3%), AT III (2.0 ± 0.4%), HDL (1.2 ± 0.9%), AT III /HDL (14.8 ± 2.1%) or TAT/HDL (23.3 ± 3.5%), respectively. TAT/HDL also had a synergistic effect with the mpl ligand, judging by the acetylcholinesterase (AchE) expression of murine megakaryocytes (2.7 fold increase). In vivo subcutaneous administration of AT III alone or TAT for 3 days significantly stimulated thrombocytosis (136% and 144%, respectively, p <0.05) and AT III/HDL showed rapid and further stimulation (150%, p <0.01). These results and the previous studies indicate that megakaryocytopoiesis is regulated by the mpl ligand, while a protease/protease inhibitor complex such as TAT, which is involved in the coagulation cascade associated with platelet consumption, might be one of the regulators in platelet production.

 
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