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布雷菲德菌素A抑制人内皮细胞中凝血酶受体的再生。

Brefeldin A inhibits thrombin receptor regeneration in human endothelial cells.

作者信息

Storck J, Vahland M, Breer T, Zimmermann E R

机构信息

Institute of Vegetative Physiology, University of Münster, Germany.

出版信息

Br J Haematol. 1997 Dec;99(3):555-61. doi: 10.1046/j.1365-2141.1997.4313241.x.

Abstract

Endothelial cells, once stimulated with thrombin, are resistant to subsequent stimulation. After a recovery period of about 60 min the cells are sensitized again for activation by thrombin. The resensitization is independent of the receptor de novo synthesis. Therefore an intracellular pool of thrombin receptors that is possibly co-localized with the Golgi apparatus has been assumed. Brefeldin A (BFA) has been used extensively to investigate the intracellular sorting of proteins because of its dramatic alteration of the structural and functional organization of the Golgi apparatus. Accordingly we have examined the effects of BFA on the regeneration of the thrombin receptor response in human umbilical vein and artery cells. The von Willebrand factor (VWF) release from Weibel-Palade vesicles and the intracellular calcium mobilization were used as physiological parameters of thrombin receptor activation. The addition of BFA (2 microg/ml) to endothelial cells or the reduction of the incubation temperature from 37 degrees C to 16 degrees C blocked the receptor response regeneration almost completely.

摘要

内皮细胞一旦受到凝血酶刺激,就会对随后的刺激产生抗性。经过约60分钟的恢复期后,细胞会再次对凝血酶激活敏感。这种再敏化与受体从头合成无关。因此,假定存在一个可能与高尔基体共定位的凝血酶受体细胞内池。布雷菲德菌素A(BFA)由于其对高尔基体结构和功能组织的显著改变,已被广泛用于研究蛋白质的细胞内分选。因此,我们研究了BFA对人脐静脉和动脉细胞中凝血酶受体反应再生的影响。血管性血友病因子(VWF)从魏贝尔-帕拉德小泡中的释放以及细胞内钙动员被用作凝血酶受体激活的生理参数。向内皮细胞中添加BFA(2微克/毫升)或将孵育温度从37℃降至16℃几乎完全阻断了受体反应的再生。

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