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关于C6胶质瘤细胞高促凝模式的分子机制

On the molecular mechanisms for the highly procoagulant pattern of C6 glioma cells.

作者信息

Fernandes R S, Kirszberg C, Rumjanek V M, Monteiro R Q

机构信息

Instituto de Bioquímica Médica, Centro de Ciências da Saúde, Universidade Federal do Rio de Janeiro, Avenida Bauhínia 400, Cidade Universitária, Ilha do Fundão, Rio de Janeiro 21941-590, Brazil.

出版信息

J Thromb Haemost. 2006 Jul;4(7):1546-52. doi: 10.1111/j.1538-7836.2006.01985.x.

Abstract

BACKGROUND

That there is a correlation between cancer and procoagulant states is well-known. C6 glioma cell line was originally induced in random-bred Wistar-Furth rats and is morphologically similar to glioblastoma multiforme, the most common aggressive glioma resistant to therapeutic interventions.

OBJECTIVES

In this study we analyzed the molecular mechanisms responsible for the highly procoagulant properties of C6 glioma cells.

METHODS

The presence of tissue factor (TF) and phosphatidylserine (PS) in C6 cells was investigated by flow-cytometric and functional analyses. The assembly of extrinsic tenase, intrinsic tenase and prothrombinase complexes on these cells was studied using enzymatic assays employing plasma or purified proteins.

RESULTS

TF was identified by flow-cytometric and functional [factor (F) Xa formation in the presence of cells and FVIIa] assays. Alternatively, conversion of FX into FXa was also observed in the presence of C6 cells, FIXa and FVIIIa. This effect was both cell- and FVIIIa-dependent, being consistent with formation of the intrinsic tenase complex. C6 cells were also able to activate prothrombin in the presence of FXa and FVa, thus supporting formation of the prothrombinase complex. This ability was similar to positive controls performed with PS-containing vesicles. Accordingly, exposure of PS on C6 cells was demonstrated by flow cytometry employing specific anti-PS antibodies. In addition, annexin V, which blocks PS binding sites, inhibited FX and prothrombin conversion by their respective C6-assembled activating complexes.

CONCLUSION

C6 glioma cells support all procoagulant reactions leading to robust thrombin formation. This ability results from concomitant TF exposure and from the presence of the anionic lipid PS at the outer leaflet of cell membrane. Therefore, this animal cell line may be used to explore new aspects concerning the role of blood coagulation proteins in tumor biology, especially those affecting the central nervous system.

摘要

背景

癌症与促凝状态之间存在关联是众所周知的。C6胶质瘤细胞系最初是在随机繁殖的Wistar - Furth大鼠中诱导产生的,其形态与多形性胶质母细胞瘤相似,多形性胶质母细胞瘤是最常见的侵袭性胶质瘤,对治疗干预具有抗性。

目的

在本研究中,我们分析了C6胶质瘤细胞具有高促凝特性的分子机制。

方法

通过流式细胞术和功能分析研究C6细胞中组织因子(TF)和磷脂酰丝氨酸(PS)的存在情况。使用血浆或纯化蛋白的酶促测定法研究这些细胞上外源性凝血酶原酶、内源性凝血酶原酶和凝血酶原酶复合物的组装。

结果

通过流式细胞术和功能测定法(在细胞和FVIIa存在下形成因子(F)Xa)鉴定出TF。此外,在C6细胞、FIXa和FVIIIa存在的情况下,也观察到FX转化为FXa。这种效应既依赖于细胞,也依赖于FVIIIa,这与内源性凝血酶原酶复合物的形成一致。C6细胞在FXa和FVa存在的情况下也能够激活凝血酶原,从而支持凝血酶原酶复合物的形成。这种能力与用含PS的囊泡进行的阳性对照相似。因此,使用特异性抗PS抗体的流式细胞术证明了PS在C6细胞上的暴露。此外,阻断PS结合位点的膜联蛋白V抑制了FX和凝血酶原被其各自在C6细胞上组装的激活复合物的转化。

结论

C6胶质瘤细胞支持所有导致大量凝血酶形成的促凝反应。这种能力源于TF的同时暴露以及细胞膜外小叶中阴离子脂质PS的存在。因此,这种动物细胞系可用于探索凝血蛋白在肿瘤生物学中的作用的新方面,特别是那些影响中枢神经系统的方面。

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