Engstad C S, Gutteberg T J, Osterud B
Department of Biochemistry, Institute of Medical Biology, University of Tromsø, Norway.
Thromb Haemost. 1997 Apr;77(4):690-6.
In the past years, our group has made several observations suggesting that blood cells behave differently and when stimulated, release different levels of cytokines, depending on which anticoagulant the blood has been drawn into. The aim of this study was therefore to compare the effect of the four anticoagulants EDTA, citrate, heparin and hirudin on monocyte, neutrophil (PMN), and platelet function in human whole blood. Human whole blood was employed as an ex vivo model of cytokine production and protein secretion, and lipopolysaccharide (LPS) induced tissue factor (TF) activity in monocytes and LPS induced tumor necrosis factor alpha (TNF alpha) release were chosen as parameters of monocyte activation. Platelet factor 4 (PF4) secretion and LPS induced lactoferrin release were chosen as parameters of platelet and PMN activation, respectively. When human whole blood was stimulated with 5 ng/ml LPS for 2 h, TF activity in monocytes isolated from EDTA blood was found to be 2.9 mU/10(6) cells, whereas TF activity in monocytes isolated from citrated, heparinized and hirudinized blood was 14.7, 24.7 and 28.5 mU/10(6) cells, respectively. TNF alpha concentrations in platelet poor plasma (PPP) isolated from whole blood stimulated with 5 ng/ml LPS for 2 h was increased with 200, 400 and 350% in citrated, heparinized and hirudinized blood respectively, as compared to EDTA blood. Next, the effect of the anticoagulant on PMN secretion was measured. PPP isolated from whole blood incubated with 5 ng/ml LPS for 90 min contained 1170 ng/ml (EDTA blood), 2880 ng/ml (citrated blood), 4220 ng/ml (heparinized blood), and 5520 ng/ml lactoferrin (hirudinized blood). When studying the platelet parameter PF4, whole blood was incubated without any stimuli for 60 min, and we found that heparin PPP contained 1180 ng/ml PF4, while hirudin PPP contained 469 ng/ml, citrate PPP 440 ng/ml, and EDTA PPP 217 ng/ml PF4, respectively. Finally, the low molecular weight heparin compound Fragmin had no enhancing effect on PF4 levels in whole blood. It is concluded that the anticoagulant used in in vitro experiments has a large influence on the parameters measured.
在过去几年中,我们团队进行了多项观察,结果表明血细胞行为各异,受到刺激时会释放不同水平的细胞因子,这取决于血液采集时所使用的抗凝剂。因此,本研究的目的是比较四种抗凝剂(乙二胺四乙酸(EDTA)、柠檬酸盐、肝素和水蛭素)对人全血中单核细胞、中性粒细胞(PMN)和血小板功能的影响。人全血被用作细胞因子产生和蛋白质分泌的体外模型,单核细胞中脂多糖(LPS)诱导的组织因子(TF)活性以及LPS诱导的肿瘤坏死因子α(TNFα)释放被选作单核细胞活化的参数。血小板因子4(PF4)分泌和LPS诱导的乳铁蛋白释放分别被选作血小板和PMN活化的参数。当用人全血与5 ng/ml LPS刺激2小时时,发现从EDTA抗凝血中分离出的单核细胞的TF活性为2.9 mU/10⁶细胞,而从柠檬酸盐抗凝血、肝素抗凝血和水蛭素抗凝血中分离出的单核细胞的TF活性分别为14.7、24.7和28.5 mU/⁶细胞。与EDTA抗凝血相比,用5 ng/ml LPS刺激2小时的全血中分离出的血小板缺乏血浆(PPP)中的TNFα浓度在柠檬酸盐抗凝血、肝素抗凝血和水蛭素抗凝血中分别增加了200%、400%和350%。接下来,测量了抗凝剂对PMN分泌的影响。用5 ng/ml LPS孵育90分钟的全血中分离出的PPP中含有1170 ng/ml(EDTA抗凝血)、2880 ng/ml(柠檬酸盐抗凝血)、4220 ng/ml(肝素抗凝血)和5520 ng/ml乳铁蛋白(水蛭素抗凝血)。在研究血小板参数PF4时,全血在无任何刺激的情况下孵育60分钟,我们发现肝素PPP中含有1180 ng/ml PF4,而水蛭素PPP中含有469 ng/ml,柠檬酸盐PPP中含有440 ng/ml,EDTA PPP中含有217 ng/ml PF4。最后,低分子量肝素化合物法安明对全血中的PF4水平没有增强作用。得出的结论是,体外实验中使用的抗凝剂对所测量的参数有很大影响。