William G Lowrie Department of Chemical and Biomolecular Engineering, The Ohio State University, 140 W. 19th Avenue, Columbus, OH 43210, USA.
Analyst. 2011 Jul 21;136(14):2996-3003. doi: 10.1039/c0an01018a. Epub 2011 Jun 6.
This study extends the in vitro understanding of the RBC storage lesion by serially analyzing the RBC's magneophoretic mobility, a property dependent on the content and oxygenation or oxidation state of hemoglobin (Hb) iron, during storage. Four prestorage leukoreduced, AS-5 preserved RBC units were stored between 1 and 6 °C for 42 days. Weekly starting on storage day 7, each unit was sampled, divided into 3 aliquots, each subjected to different reactions: one aliquot was exposed to room air to produce oxyhemoglobin (oxyHb), another aliquot was mixed with sodium nitrite to produce methemoglobin (metHb), while the third aliquot was desaturated of oxygen (deoxyhemoglobin, deoxyHb) using nitrogen gas. These aliquots were placed into a cell tracking velocimetry (CTV) apparatus which measured both the settling velocity (u(s)) of the RBCs as well as their magnetically induced velocity (u(m)). The u(m)/u(s) ratio depends on the oxygenation state of the hemoglobin and the quantity of iron within the RBC. The RBC density was measured by percoll centrifugation. There was a significant reduction in the u(m)/u(s) ratio for the deoxyHb RBC aliquot as storage time elapsed, with a smaller but still significant reduction in the u(m)/u(s) ratio for the metHb aliquot. The average RBC density decreased very slightly during storage, as determined by the percoll centrifugation technique, although the average settling velocity (another measure of cell density) seemed to fluctuate during storage. The decrease in magnetophoretic mobility of the deoxyHb portion is explicable either by Hb's increased affinity for oxygen during storage, or else a loss of iron from the cells.
本研究通过连续分析 RBC 的电泳迁移率(一种依赖于血红蛋白(Hb)铁的含量和氧合或氧化状态的特性),扩展了对 RBC 储存损伤的体外理解。4 个储存前白细胞减少、AS-5 保存的 RBC 单位在 1 至 6°C 下储存 42 天。从储存第 7 天开始每周,从每个单位中取样,分为 3 个等分,每个等分分别进行不同的反应:一个等分暴露于室气中以产生氧合血红蛋白(oxyHb),另一个等分与亚硝酸钠混合以产生高铁血红蛋白(metHb),而第三个等分通过氮气使氧气(脱氧血红蛋白,deoxyHb)脱氧。这些等分被放入细胞跟踪速度测量仪(CTV)中,该仪器同时测量 RBC 的沉降速度(u(s))和其受磁场诱导的速度(u(m))。u(m)/u(s) 的比值取决于血红蛋白的氧合状态和 RBC 内铁的数量。通过 Percoll 离心测量 RBC 密度。随着储存时间的延长,脱氧 Hb RBC 等分的 u(m)/u(s) 比值显著降低,而 metHb 等分的 u(m)/u(s) 比值虽然较小但仍有显著降低。通过 Percoll 离心技术确定,RBC 密度在储存过程中仅略有下降,尽管平均沉降速度(细胞密度的另一种测量方法)在储存过程中似乎波动。脱氧 Hb 部分的电泳迁移率下降可以解释为 Hb 在储存过程中对氧气的亲和力增加,或者细胞内铁的损失。