首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >Tissue factor encryption/de-encryption is not altered in the absence of the cytoplasmic domain.
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Tissue factor encryption/de-encryption is not altered in the absence of the cytoplasmic domain.

机译:在没有胞质结构域的情况下,组织因子加密/解密不会改变。

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摘要

Since the cytoplasmic domain of tissue factor (TF) appears to have a role in TF function beyond coagulation, experiments were conducted to determine whether the cytoplasmic domain also has a role in regulating procoagulant activity of TF present in the cell membrane. TF encryption was quantitated in human YU-SITI, U87-MG, and mouse 3T3 cells which were transfected for expression of human tissue factor or a construct lacking the cytoplasmic domain (TF(CD)). Comparison of intact cells (encrypted) with fully disrupted cells (de-encrypted) showed that TF and TF(CD) were equally encrypted with respect to function in fX activation. Moreover, cells expressing TF and TF(CD) were indistinguishable in their procoagulant responses to A23187-calcium and varied concentrations of nonionic detergents. TF in membrane vesicles spontaneously shed by U87-MG cells was largely, but incompletely, de-encrypted, and the degree of de-encryption was independent of the cytoplasmic domain. We conclude that the predominant mechanism(s) for encrypting TF procoagulant activity is independent of the cytoplasmic domain.
机译:由于组织因子(TF)的胞质结构域似乎在凝血功能之外还对TF功能起作用,因此进行了实验以确定胞质域是否也对调节细胞膜中存在的TF的促凝活性起作用。在人类YU-SITI,U87-MG和小鼠3T3细胞中对TF加密进行了定量,将其转染以表达人类组织因子或缺乏细胞质结构域的构建体(TF(CD))。完整细胞(已加密)与完全破裂的细胞(已解密)的比较显示,就fX激活的功能而言,TF和TF(CD)被均等地加密了。此外,表达TF和TF(CD)的细胞对A23187-钙和不同浓度的非离子去污剂的促凝反应是无法区分的。 U87-MG细胞自发脱落的膜囊泡中的TF在很大程度上但不完全地被解密,并且解密的程度与细胞质域无关。我们得出结论,加密TF促凝活性的主要机制独立于细胞质域。

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