Öhlinger Thomas, Müllner Ernst W, Fritz Magdalena, Werning Maike, Baron-Stefaniak Joanna, Jungbauer Christof, Baron David M, Salzer Ulrich
Center for Medical Biochemistry, Max Perutz Labs (MPL), Medical University of Vienna, Vienna, Austria.
Department of Anaesthesia, Intensive Care Medicine and Pain Medicine, Medical University of Vienna, Vienna, Austria.
Front Physiol. 2022 Nov 25;13:1021553. doi: 10.3389/fphys.2022.1021553. eCollection 2022.
Storage of packed red blood cells is associated with changes in erythrocytes that over time increasingly impair cellular function and potentially contribute to adverse effects associated with blood transfusion. Exposure of phosphatidylserine at the outer membrane leaflet of erythrocytes and shedding of microvesicles (MVs) during packed red blood cell storage are alterations assumed to increase the risk of prothrombotic events in recipients. Here, we used rotational thromboelastometry to study the coagulation process in blood samples with erythrocytes from stored PRBCs reconstituted with freshly prepared platelet-rich plasma. We explored the influence of following effects on the coagulation process: 1) PRBC storage duration, 2) differences between erythrocytes from stored PRBCs compared to freshly drawn erythrocytes, and 3) the contribution of added MVs. Interestingly, despite of a higher fraction of PS-positive cells, erythrocytes from PRBCs stored for 6 weeks revealed longer clotting times than samples with erythrocytes stored for 2 or 4 weeks. Further, clotting times and clot formation times were considerably increased in samples reconstituted with erythrocytes from stored PRBCs as compared to fresh erythrocytes. Moreover, MVs added to reconstituted samples elicited only comparably small and ambiguous effects on coagulation. Thus, this study provides no evidence for an amplified clotting process from prolonged storage of PRBCs but on the contrary implicates a loss of function, which may be of clinical significance in massive transfusion. Our observations add to the increasing body of evidence viewing erythrocytes as active players in the clotting process.
浓缩红细胞的储存与红细胞的变化相关,随着时间的推移,这些变化会越来越损害细胞功能,并可能导致与输血相关的不良反应。在浓缩红细胞储存过程中,红细胞外膜小叶上磷脂酰丝氨酸的暴露和微泡(MVs)的脱落被认为是增加受血者发生血栓前事件风险的改变。在这里,我们使用旋转血栓弹力图来研究用新鲜制备的富含血小板血浆重构的储存浓缩红细胞的血样中的凝血过程。我们探讨了以下因素对凝血过程的影响:1)浓缩红细胞的储存时间,2)储存浓缩红细胞中的红细胞与新鲜抽取的红细胞之间的差异,以及3)添加的微泡的作用。有趣的是,尽管PS阳性细胞的比例较高,但储存6周的浓缩红细胞的凝血时间比储存2周或4周的红细胞样本更长。此外,与新鲜红细胞相比,用储存浓缩红细胞中的红细胞重构的样本的凝血时间和凝块形成时间显著增加。此外,添加到重构样本中的微泡对凝血的影响相对较小且不明确。因此,本研究没有提供证据表明浓缩红细胞长时间储存会导致凝血过程增强,相反,提示了功能丧失,这在大量输血中可能具有临床意义。我们的观察结果进一步证明红细胞在凝血过程中是积极参与者。