Hageman factor, platelets and polyphosphates: early history and recent connection

被引:31
作者
Caen, J. [4 ]
Wu, Q. [1 ,2 ,3 ,5 ]
机构
[1] Cleveland Clin, Dept Mol Cardiol, Cleveland, OH 44195 USA
[2] Cleveland Clin, Dept Hypertens & Nephrol, Cleveland, OH 44195 USA
[3] Cleveland Clin, Lerner Res Inst, Cleveland, OH 44195 USA
[4] FFCSA, F-75007 Paris, France
[5] Soochow Univ, Affiliated Hosp 1, Jiangsu Inst Hematol, Cyrus Tang Hematol Ctr, Suzhou, Peoples R China
关键词
coagulation; factor XII; platelet; polyphosphate; COAGULATION-FACTOR-XII; KALLIKREIN-KININ SYSTEM; ANION-BINDING EXOSITE; BLOOD-COAGULATION; INORGANIC POLYPHOSPHATE; TISSUE FACTOR; FACTOR-VII; IN-VIVO; THROMBUS FORMATION; INTRINSIC PATHWAY;
D O I
10.1111/j.1538-7836.2010.03893.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Platelet activation and blood coagulation are essential for hemostasis and contribute to a variety of other biological processes such as inflammation, complement activation and tissue repair. Factor (F)XII, originally called Hageman factor, plays an important role in the kallikrein-kinin system by activating prekallikrein. In the 1960s, a platelet activity that promoted FXII activation was identified but its biochemical nature remained unknown. Inorganic polyphosphates (poly P) are polymers that consist of many phosphate residues linked by phosphoanhydride bonds. These polymers exist in all living organisms. In bacteria, poly P is important for growth and survival. Recently, poly P has been identified in human platelet dense granules. Studied have shown that upon platelet activation and secretion, poly P activates FXII, indicating that it is most likely the elusive platelet FXII activator. Poly P also regulates coagulation and fibrinolysis. In this review, we focus on early studies of FXII and the identification of platelet FXII activation activity, and discuss recent findings of poly P in FXII activation and coagulation.
引用
收藏
页码:1670 / 1674
页数:5
相关论文
共 73 条
[11]   Thrombus formation in vivo [J].
Furie, B ;
Furie, BC .
JOURNAL OF CLINICAL INVESTIGATION, 2005, 115 (12) :3355-3362
[12]   FACTOR-XI ACTIVATION IN A REVISED MODEL OF BLOOD-COAGULATION [J].
GAILANI, D ;
BROZE, GJ .
SCIENCE, 1991, 253 (5022) :909-912
[13]   The intrinsic pathway of coagulation:: a target for treating thromboembolic disease? [J].
Gailani, D. ;
Renne, T. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2007, 5 (06) :1106-1112
[14]   Intrinsic pathway of coagulation and arterial thrombosis [J].
Gailani, David ;
Renne, Thomas .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2007, 27 (12) :2507-2513
[15]   THROMBASTHENIA - STUDIES ON 3 CASES [J].
HARDISTY, RM ;
DORMANDY, KM ;
HUTTON, RA .
BRITISH JOURNAL OF HAEMATOLOGY, 1964, 10 (03) :371-&
[16]   KAOLIN CLOTTING TIME OF PLATELET-RICH PLASMA - A TEST OF PLATELET FACTOR-3 AVAILABILITY [J].
HARDISTY, RM ;
HUTTON, RA .
BRITISH JOURNAL OF HAEMATOLOGY, 1965, 11 (03) :258-&
[17]   INORGANIC POLYPHOSPHATES IN BIOLOGY - STRUCTURE METABOLISM AND FUNCTION [J].
HAROLD, FM .
BACTERIOLOGICAL REVIEWS, 1966, 30 (04) :772-&
[18]   The molecular basis of innate immunity in the horseshoe crab [J].
Iwanaga, S .
CURRENT OPINION IN IMMUNOLOGY, 2002, 14 (01) :87-95
[19]   Factor VII-activating protease (FSAP): Vascular functions and role in atherosclerosis [J].
Kanse, Sandip M. ;
Parahuleva, Mariana ;
Muhl, Lars ;
Kemkes-Matthes, Bettina ;
Sedding, Daniel ;
Preissner, Klaus T. .
THROMBOSIS AND HAEMOSTASIS, 2008, 99 (02) :286-289
[20]   HEPSIN, A PUTATIVE MEMBRANE-ASSOCIATED SERINE-PROTEASE, ACTIVATES HUMAN FACTOR-VII AND INITIATES A PATHWAY OF BLOOD-COAGULATION ON THE CELL-SURFACE LEADING TO THROMBIN FORMATION [J].
KAZAMA, Y ;
HAMAMOTO, T ;
FOSTER, DC ;
KISIEL, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (01) :66-72