J Thromb Haemost. 2014 May;12(5):690-700. doi: 10.1111/jth.12532.
Recent studies have shown that factor VIIa binds to endothelial cell protein C receptor(EPCR), a cellular receptor for protein C and activated protein C. At present, the physiologic significance of FVIIa interaction with EPCR in vivo remains unclear.
To investigate whether exogenously administered FVIIa, by binding to EPCR, induces a barrier protective effect in vivo.
Lipopolysaccharide(LPS)-induced vascular leakage in the lung and kidney,and vascular endothelial growth factor (VEGF)-induced vascular leakage in the skin, were used to evaluate the FVIIa-induced barrier protective effect. Wild-type, EPCR-deficient, EPCR-overexpressing and hemophilia A mice were used in the studies.
Administration ofFVIIa reduced LPS-induced vascular leakage in the lung and kidney; the FVIIa-induced barrier protective effect was attenuated in EPCR-deficient mice. The extent of VEGF-induced vascular leakage in the skin was highly dependent on EPCR expression levels. Therapeutic concentrations of FVIIa attenuated VEGF-induced vascular leakage in control mice but not in EPCR-deficient mice.Blockade of FVIIa binding to EPCR with a blocking mAb completely attenuated the FVIIa-induced barrier protective effect. Similarly, administration of protease activated receptor 1 antagonist blocked the FVIIa induced barrier protective effect. Hemophilic mice showed increased vascular permeability, and administration of therapeutic concentrations of FVIIa improved barrier integrity in these mice.
This is the first study to demonstrate that FVIIa binding to EPCR leads to a barrier protective effect in vivo. This finding may have clinical relevance, as it indicates additional advantages of using FVIIa in treating hemophilic patients.
最近的研究表明,因子 VIIa 与内皮细胞蛋白 C 受体(EPCR)结合,EPCR 是蛋白 C 和活化蛋白 C 的细胞受体。目前,因子 VIIa 与 EPCR 在体内相互作用的生理意义尚不清楚。
研究外源性给予因子 VIIa 通过与 EPCR 结合是否在体内诱导屏障保护作用。
采用脂多糖(LPS)诱导的肺和肾血管渗漏以及血管内皮生长因子(VEGF)诱导的皮肤血管渗漏来评价因子 VIIa 诱导的屏障保护作用。研究中使用了野生型、EPCR 缺陷型、EPCR 过表达型和血友病 A 小鼠。
给予因子 VIIa 可减轻 LPS 诱导的肺和肾血管渗漏;EPCR 缺陷型小鼠的因子 VIIa 诱导的屏障保护作用减弱。皮肤中 VEGF 诱导的血管渗漏程度高度依赖于 EPCR 表达水平。治疗浓度的因子 VIIa 可减轻对照小鼠中 VEGF 诱导的血管渗漏,但不能减轻 EPCR 缺陷型小鼠中的血管渗漏。用阻断性单克隆抗体阻断因子 VIIa 与 EPCR 的结合可完全阻断因子 VIIa 诱导的屏障保护作用。同样,给予蛋白酶激活受体 1 拮抗剂也可阻断因子 VIIa 诱导的屏障保护作用。血友病 A 小鼠表现出血管通透性增加,给予治疗浓度的因子 VIIa 可改善这些小鼠的屏障完整性。
这是第一项证明因子 VIIa 与 EPCR 结合可在体内诱导屏障保护作用的研究。这一发现可能具有临床意义,因为它表明在治疗血友病 A 患者时使用因子 VIIa 具有额外的优势。