Oh Joo-Yeun, Stapley Ryan, Harper Victoria, Marques Marisa B, Patel Rakesh P
Department of Pathology.
Center for Free Radical Biology, University of Alabama at Birmingham, Birmingham, Alabama.
Transfusion. 2015 Dec;55(12):2967-78. doi: 10.1111/trf.13248. Epub 2015 Jul 22.
Storage-dependent damage to red blood cells (RBCs) varies significantly. Identifying RBC units that will undergo higher levels of hemolysis during storage may allow for more efficient inventory management decision-making. Oxidative-stress mediates storage-dependent damage to RBCs and will depend on the oxidant:antioxidant balance. We reasoned that this balance or redox tone will serve as a determinant of how a given RBC unit stores and that its assessment in "young" RBCs will predict storage-dependent hemolysis.
RBCs were sampled from bags and segments stored for 7 to 42 days. Redox tone was assessed by nitrite oxidation kinetics and peroxiredoxin-2 (Prx-2) oxidation. In parallel, hemolysis was assessed by measuring cell-free hemoglobin (Hb) and free heme (hemin). Correlation analyses were performed to determine if Day 7 measurements predicted either the level of hemolysis at Day 35 or the increase in hemolysis during storage.
Higher Day 7 Prx-2 oxidation was associated with higher Day 35 Prx-2 oxidation, suggesting that early assessment of this variable may identify RBCs that will incur the most oxidative damage during storage. RBCs that oxidized nitrite faster on Day 7 were associated with the greatest levels of storage-dependent hemolysis and increases in Prx-2 oxidation. An inverse relationship between storage-dependent changes in oxyhemoglobin and free heme was observed underscoring an unappreciated reciprocity between these molecular species. Moreover, free heme was higher in the bag compared to paired segments, with opposite trends observed for free Hb.
Measurement of Prx-2 oxidation and nitrite oxidation kinetics early during RBC storage may predict storage-dependent damage to RBC including hemolysis-dependent formation of free Hb and heme.
红细胞(RBC)的储存依赖性损伤差异显著。识别在储存期间将经历更高水平溶血的红细胞单位可能有助于做出更有效的库存管理决策。氧化应激介导红细胞的储存依赖性损伤,并且将取决于氧化剂与抗氧化剂的平衡。我们推断这种平衡或氧化还原状态将决定给定红细胞单位的储存方式,并且在“年轻”红细胞中对其进行评估将预测储存依赖性溶血。
从储存7至42天的血袋和血段中采集红细胞。通过亚硝酸盐氧化动力学和过氧化物酶2(Prx-2)氧化评估氧化还原状态。同时,通过测量游离血红蛋白(Hb)和游离血红素(高铁血红素)评估溶血情况。进行相关性分析以确定第7天的测量值是否能预测第35天的溶血水平或储存期间溶血的增加。
第7天高的Prx-2氧化与第35天高的Prx-2氧化相关,表明对该变量的早期评估可能识别出在储存期间将遭受最大氧化损伤的红细胞。第7天亚硝酸盐氧化更快的红细胞与最高水平的储存依赖性溶血和Prx-2氧化增加相关。观察到氧合血红蛋白和游离血红素的储存依赖性变化之间呈负相关,突出了这些分子物种之间未被重视的相互关系。此外,与配对血段相比,血袋中的游离血红素更高,而游离Hb则呈现相反趋势。
在红细胞储存早期测量Prx-2氧化和亚硝酸盐氧化动力学可能预测红细胞的储存依赖性损伤,包括溶血依赖性游离Hb和血红素的形成。