Mulder A B, Hegge-Paping K S, Magielse C P, Blom N R, Smit J W, van der Meer J, Hallie M R, Bom V J
Division of Haemostasis, University Hospital, Groningen, The Netherlands.
Blood. 1994 Sep 1;84(5):1559-66.
Because there is no consensus regarding the precise distribution of induced endothelial tissue factor (TF), we studied TF activity in and on tumor necrosis factor alpha-stimulated cultured human umbilical vein endothelial cells (ECs) and their underlying matrix. TF was mainly expressed on the cell surface. Only small traces were found on the apical surface suggesting that TF is predominantly located on the basolateral side of the cell membrane. The presence of TF on the cell surface was confirmed by flow cytometry. Subendothelial TF activity appeared to be dependent upon the procedure used to remove the stimulated EC monolayer. Whereas ammonium hydroxide or hypotonic lysis resulted in relatively high levels of matrix-associated TF, virtually no TF was found on the matrix after mild enzymatic detachment of stimulated ECs. Cell removal with EDTA resulted in intermediate levels of matrix-associated TF. Neither the enzymatic treatment nor EDTA degraded or removed this TF activity. Similar patterns were observed for matrix-associated TF antigen and EC surface markers. Electron microscopic analysis showed cell fragments on the matrix after monolayer lysis. The findings strongly suggest that induced endothelial TF associated with the subendothelial matrix actually represents TF on EC remnants.
由于关于诱导型内皮组织因子(TF)的精确分布尚无共识,我们研究了肿瘤坏死因子α刺激的培养人脐静脉内皮细胞(ECs)及其下层基质中及表面的TF活性。TF主要表达于细胞表面。仅在顶端表面发现少量痕迹,这表明TF主要位于细胞膜的基底外侧。通过流式细胞术证实了细胞表面存在TF。内皮下TF活性似乎取决于用于去除刺激的EC单层的方法。氢氧化铵或低渗裂解导致相对高水平的与基质相关的TF,而在温和酶法分离刺激的ECs后,在基质上几乎未发现TF。用EDTA去除细胞导致与基质相关的TF处于中等水平。酶处理和EDTA均未降解或去除这种TF活性。对于与基质相关的TF抗原和EC表面标志物观察到类似模式。电子显微镜分析显示单层裂解后基质上有细胞碎片。这些发现强烈表明,与内皮下基质相关的诱导型内皮TF实际上代表EC残余物上的TF。