Tzounakas Vassilis L, Anastasiadi Alkmini T, Lekka Marilena E, Papageorgiou Effie G, Stamoulis Konstantinos, Papassideri Issidora S, Kriebardis Anastasios G, Antonelou Marianna H
Section of Cell Biology and Biophysics, Department of Biology, School of Science, National and Kapodistrian University of Athens (NKUA), Athens, Greece.
Laboratory of Biochemistry, Department of Chemistry, University of Ioannina, Ioannina, Greece.
Front Physiol. 2022 Feb 8;13:840995. doi: 10.3389/fphys.2022.840995. eCollection 2022.
Red blood cells (RBCs) release hemoglobin (Hb)-containing extracellular vesicles (EVs) throughout their lifespan in the circulation, and especially during senescence, by spleen-facilitated vesiculation of their membrane. During aging under blood bank conditions, the RBCs lose Hb, both in soluble form and inside EVs that accumulate as a part of storage lesion in the supernatant of the unit. Spontaneous hemolysis and vesiculation are increasingly promoted by the storage duration, but little is known about any physiological linkage between them. In the present study, we measured the levels of total extracellular and EV-enclosed Hb (EV-Hb) in units of whole blood ( = 36) or packed RBCs stored in either CPDA-1 ( = 99) or in CPD-SAGM additive solution ( = 46), in early, middle, and late storage. The spectrophotometry data were subjected to statistical analysis to detect possible correlation(s) between storage hemolysis and EV-Hb, as well as the threshold (if any) that determines the area of this dynamic association. It seems that the percentage of EV-Hb is negatively associated with hemolysis levels from middle storage onward by showing low to moderate correlation profiles in all strategies under investigation. Moreover, 0.17% storage hemolysis was determined as the potential cut-off, above which this inverse correlation is evident in non-leukoreduced CPDA units. Notably, RBC units with hemolysis levels > 0.17% are characterized by higher percentage of nanovesicles (<100 nm) over typical microvesicles (100-400 nm) compared with the lower hemolysis counterparts. Our results suggest an ordered loss of Hb during RBC accelerated aging that might fuel targeted research to elucidate its mechanistic basis.
红细胞(RBC)在其循环寿命期间,尤其是在衰老过程中,通过脾脏促进其细胞膜的囊泡化,释放出含有血红蛋白(Hb)的细胞外囊泡(EV)。在血库条件下储存的老化过程中,红细胞会以可溶性形式以及作为单位上清液中储存损伤一部分而积累的细胞外囊泡内的形式丢失血红蛋白。储存持续时间会越来越多地促进自发溶血和囊泡化,但它们之间的任何生理联系却知之甚少。在本研究中,我们测量了全血单位(n = 36)或保存在CPDA-1(n = 99)或CPD-SAGM添加剂溶液(n = 46)中的浓缩红细胞在储存早期、中期和晚期的总细胞外和细胞外囊泡包裹的血红蛋白(EV-Hb)水平。对分光光度法数据进行统计分析,以检测储存溶血与EV-Hb之间可能的相关性,以及确定这种动态关联区域的阈值(如果有的话)。似乎从储存中期开始,EV-Hb的百分比与溶血水平呈负相关,在所有研究策略中均呈现低到中等的相关特征。此外,确定0.17%的储存溶血为潜在的临界值,高于此值,这种负相关在未白细胞滤除的CPDA单位中很明显。值得注意的是,与溶血水平较低的对应物相比,溶血水平>0.17%的红细胞单位的纳米囊泡(<100 nm)百分比高于典型的微囊泡(100 - 400 nm)。我们的结果表明,在红细胞加速衰老过程中血红蛋白有序丢失,这可能推动有针对性的研究以阐明其机制基础。