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Contact pathway of coagulation and inflammation

The contact system, also named as plasma kallikrein-kinin system, consists of three serine proteinases: coagulation factors XII (FXII) and XI (FXI), and plasma prekallikrein (PK), and the nonenzymatic cofactor high molecular weight kininogen (HK). This system has been investigated actively for more...

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Autor principal: Wu, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421925/
https://www.ncbi.nlm.nih.gov/pubmed/25949215
http://dx.doi.org/10.1186/s12959-015-0048-y
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author Wu, Yi
author_facet Wu, Yi
author_sort Wu, Yi
collection PubMed
description The contact system, also named as plasma kallikrein-kinin system, consists of three serine proteinases: coagulation factors XII (FXII) and XI (FXI), and plasma prekallikrein (PK), and the nonenzymatic cofactor high molecular weight kininogen (HK). This system has been investigated actively for more than 50 years. The components of this system and their interactions have been elucidated from in vitro experiments, which indicates that this system is prothrombotic by activating intrinsic pathway, and proinflammatory by producing bioactive peptide bradykinin. Although the activation of the contact system have been implicated in various types of human disease, in only a few instances is its role clearly defined. In the last 10 years, our understanding of the contact system, particularly its biology and (patho)physiology has greatly increased through investigations using gene-modified animal models. In this review we will describe a revitalized view of the contact system as a critical (patho)physiologic mediator of coagulation and inflammation.
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spelling pubmed-44219252015-05-07 Contact pathway of coagulation and inflammation Wu, Yi Thromb J Review The contact system, also named as plasma kallikrein-kinin system, consists of three serine proteinases: coagulation factors XII (FXII) and XI (FXI), and plasma prekallikrein (PK), and the nonenzymatic cofactor high molecular weight kininogen (HK). This system has been investigated actively for more than 50 years. The components of this system and their interactions have been elucidated from in vitro experiments, which indicates that this system is prothrombotic by activating intrinsic pathway, and proinflammatory by producing bioactive peptide bradykinin. Although the activation of the contact system have been implicated in various types of human disease, in only a few instances is its role clearly defined. In the last 10 years, our understanding of the contact system, particularly its biology and (patho)physiology has greatly increased through investigations using gene-modified animal models. In this review we will describe a revitalized view of the contact system as a critical (patho)physiologic mediator of coagulation and inflammation. BioMed Central 2015-05-06 /pmc/articles/PMC4421925/ /pubmed/25949215 http://dx.doi.org/10.1186/s12959-015-0048-y Text en © Wu; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Wu, Yi
Contact pathway of coagulation and inflammation
title Contact pathway of coagulation and inflammation
title_full Contact pathway of coagulation and inflammation
title_fullStr Contact pathway of coagulation and inflammation
title_full_unstemmed Contact pathway of coagulation and inflammation
title_short Contact pathway of coagulation and inflammation
title_sort contact pathway of coagulation and inflammation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4421925/
https://www.ncbi.nlm.nih.gov/pubmed/25949215
http://dx.doi.org/10.1186/s12959-015-0048-y
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