Putting polyphosphates to the test: evidence against platelet-induced activation of factor XII

被引:41
作者
Faxaelv, Lars [1 ]
Boknaes, Niklas [1 ]
Stroem, Jakob O. [1 ]
Tengvall, Pentti
Theodorsson, Elvar [1 ,2 ]
Ramstroem, Sofia [1 ]
Lindahl, Tomas L. [1 ]
机构
[1] Linkoping Univ, Dept Clin & Expt Med, SE-58185 Linkoping, Sweden
[2] Univ Gothenburg, Sahlgrenska Acad, Dept Biomaterials, Inst Clin Sci, Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
COAGULATION-FACTOR-XII; ARTERIAL THROMBUS FORMATION; BLOOD-COAGULATION; IN-VIVO; CONTACT ACTIVATION; CLOTTING TIME; RECEPTOR; MICE; BIOMATERIALS; RESPONSES;
D O I
10.1182/blood-2013-05-499384
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The recent claim that stimulated platelets activate the intrinsic pathway of coagulation by the release of polyphosphates has been considered a breakthrough in hemostasis research. In little more than 3 years, the original publication by Muller et al has been cited >100 times. However, none of the citing articles has sought to independently validate this potentially paradigm-shifting concept. To this end, we performed extensive experimentation in vitro and in vivo in an attempt to verify the claim that factor XII (FXII) is primarily activated by stimulated platelets. In contrast to the original assertion, platelet-derived polyphosphates were found to be weak activators of FXII, with a FXIIa-generating activity of <10% compared with equivalent concentrations of kaolin. Using different coagulation assays, it was shown that platelet contribution to whole blood coagulation was unrelated to the generation of activated FXII in vitro. Additionally, key results used to verify the hypothesis in the original study in vivo were found to be irreproducible. We conclude that platelet-derived polyphosphates are not physiologically relevant activators of FXII.
引用
收藏
页码:3818 / 3824
页数:7
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