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全身炎症性疾病中的 GAS6:感染与非感染。

GAS6 in systemic inflammatory diseases: with and without infection.

机构信息

Department of Cell Death and Proliferation, Institute for Biomedical Research of Barcelona (IIBB-CSIC-IDIBAPS), C/Roselló 161-6°, 08036 Barcelona, Spain.

出版信息

Crit Care. 2010;14(5):1003. doi: 10.1186/cc9263. Epub 2010 Oct 21.

Abstract

Vitamin K-dependent proteins are not only essential regulators of blood coagulation. A recent paper in Critical Care describes the levels of the vitamin K-dependent GAS6 and the soluble form of its receptor Axl in plasma from patients with sepsis of systemic inflammation. The results confirm that GAS6 is elevated during septicemia, but the fact that inflammatory conditions without infection produce a similar effect suggests it is inflammation that induces the synthesis of GAS6, rather than the interactions with bacteria or other infectious agents. The soluble form of the GAS6 receptor Axl was induced less compared with the effect observed in GAS6. This is important as the two proteins form an inactive complex in plasma, suggesting that a functional GAS6 form could be synthesized under these conditions. GAS6 has been proposed as a broad regulator of the innate immune response. GAS6 synthesis is therefore likely to be a regulatory mechanism during systemic inflammation. Recent advances provide the necessary tools for further research, including genetic screenings of the components of this system.

摘要

维生素 K 依赖性蛋白不仅是血液凝血的重要调节剂。《危重病医学》上的一篇新论文描述了全身性炎症反应性脓毒症患者血浆中维生素 K 依赖性生长停滞特异性 6 蛋白(GAS6)及其受体 Axl 的可溶性形式的水平。结果证实 GAS6 在败血症期间升高,但没有感染的炎症状态产生类似影响的事实表明,诱导 GAS6 合成的是炎症,而不是与细菌或其他传染性病原体的相互作用。与在 GAS6 中观察到的作用相比,GAS6 受体 Axl 的可溶性形式的诱导作用较小。这很重要,因为这两种蛋白质在血浆中形成无活性复合物,表明在这些条件下可以合成具有功能的 GAS6 形式。GAS6 已被提议作为先天免疫反应的广泛调节剂。因此,GAS6 的合成可能是全身炎症反应的一种调节机制。最近的进展为进一步的研究提供了必要的工具,包括对该系统成分的遗传筛选。

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