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蛋白Z,一种寻找病理学关联的蛋白质。

Protein Z, a protein seeking a pathology.

作者信息

Vasse Marc

机构信息

Groupe MERCI (EA 3829) & IHURBM, Faculté de Médecine & Pharmacie de Rouen, 22 Boulevard Gambetta, 76038 Rouen cedex, France.

出版信息

Thromb Haemost. 2008 Oct;100(4):548-56.

Abstract

Protein Z (PZ) is a vitamin K-dependent factor identified in human plasma in 1984 characterized by an homology with other vitamin K-dependent factors (factor VII, IX, X, protein C). In contrast to these factors, PZ does not possess any enzymatic activity but is involved as a cofactor in the down-regulation of coagulation by forming a complex with the protein Z-dependent protease inhibitor (ZPI). ZPI inhibits the activated factor X (FXa) on phospholipid surface. In mice, the disruption of PZ gene is asymptomatic, but the association with the factor V Leiden mutation leads to a quasi complete mortality during the neonatal period with microvascular thrombosis. In humans, PZ is characterized by an unusual wide distribution in plasma, and a major decrease induced by warfarin. Isolated PZ deficiency does not seem to constitute a risk for venous thrombosis, but a severe PZ deficiency could increase the risk of well recognized venous thrombotic risk factors such as factor V Leiden, G20210A mutation or hyperhomocysteinemia. Unexpectedly, a relationship between PZ deficiency and ischemic arterial diseases such as stroke, acute coronary syndromes or peripheral arterial disease was described but not confirmed by all studies. PZ deficiency could be also a risk factor for early fetal losses, and increases the arterial risk in antiphospholipid syndrome. This review analyzes the different studies so far published and discusses the various results obtained in order to understand whether or not protein Z deficiency could be considered as an arterial ischemic risk factor.

摘要

蛋白Z(PZ)是1984年在人血浆中发现的一种维生素K依赖因子,其与其他维生素K依赖因子(因子VII、IX、X、蛋白C)具有同源性。与这些因子不同的是,PZ不具备任何酶活性,而是作为辅因子参与凝血的下调过程,它通过与蛋白Z依赖的蛋白酶抑制剂(ZPI)形成复合物来实现这一作用。ZPI在磷脂表面抑制活化的因子X(FXa)。在小鼠中,PZ基因的缺失没有症状,但与因子V莱顿突变相关时会导致新生儿期几乎完全死亡,并伴有微血管血栓形成。在人类中,PZ的特点是在血浆中分布异常广泛,且华法林会使其大幅减少。孤立的PZ缺乏似乎不构成静脉血栓形成的风险,但严重的PZ缺乏可能会增加一些已被充分认识的静脉血栓形成风险因素的风险,如因子V莱顿突变、G20210A突变或高同型半胱氨酸血症。出乎意料的是,有研究描述了PZ缺乏与缺血性动脉疾病(如中风、急性冠状动脉综合征或外周动脉疾病)之间的关系,但并非所有研究都证实了这一点。PZ缺乏也可能是早期胎儿丢失的一个风险因素,并增加抗磷脂综合征中的动脉风险。这篇综述分析了迄今为止发表的不同研究,并讨论了所获得的各种结果,以了解蛋白Z缺乏是否可被视为一种动脉缺血风险因素。

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