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蛋白Z:一种新型血栓形成因子的“光影”

Protein Z: "light and shade" of a new thrombotic factor.

作者信息

Sofi Francesco, Cesari Francesca, Fedi Sandra, Abbate Rosanna, Gensini Gian Franco

机构信息

Department of Medical and Surgical Critical Care, Thrombosis Centre, University of Florence, Italy.

出版信息

Clin Lab. 2004;50(11-12):647-52.

Abstract

Protein Z is a vitamin K-dependent plasma protein described in its human form in 1984. The amino acid sequence of protein Z shows wide homology with many coagulation factors, such as VII, IX, X, and protein C. However, in contrast to other vitamin K-dependent coagulation factors, protein Z is not a serine protease because of the lack of the active centre in its amino acid sequence. The physiological function of protein Z has been uncertain for many years. In vitro and in vivo studies recently suggested that protein Z plays an important role in inhibiting coagulation, as it serves as cofactor for the inactivation of activated factor X by forming a complex with the plasma protein Z-dependent protease inhibitor. The role of alterations of the protein Z levels has been evaluated in different disease states, with conflicting findings. Most of these studies were performed on ischemic vascular diseases. Recently, the possible role of protein Z deficiency in the occurrence of cardiovascular diseases has been evaluated.

摘要

蛋白Z是一种维生素K依赖的血浆蛋白,于1984年以其人类形式被描述。蛋白Z的氨基酸序列与许多凝血因子,如因子VII、IX、X和蛋白C,具有广泛的同源性。然而,与其他维生素K依赖的凝血因子不同,蛋白Z不是丝氨酸蛋白酶,因为其氨基酸序列中缺乏活性中心。多年来,蛋白Z的生理功能一直不确定。最近的体外和体内研究表明,蛋白Z在抑制凝血中起重要作用,因为它通过与血浆蛋白Z依赖的蛋白酶抑制剂形成复合物,作为灭活活化因子X的辅因子。在不同疾病状态下评估了蛋白Z水平改变的作用,但结果相互矛盾。这些研究大多是针对缺血性血管疾病进行的。最近,评估了蛋白Z缺乏在心血管疾病发生中的可能作用。

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