Man Yuncheng, An Ran, Monchamp Karamoja, Sekyonda Zoe, Kucukal Erdem, Federici Chiara, Wulftange William J, Goreke Utku, Bode Allison, Sheehan Vivien A, Gurkan Umut A
Department of Mechanical and Aerospace Engineering, Case Western Reserve University, Cleveland, OH, United States.
Division of Hematology and Oncology, School of Medicine, Case Western Reserve University, Cleveland, OH, United States.
Front Physiol. 2022 Aug 25;13:954106. doi: 10.3389/fphys.2022.954106. eCollection 2022.
Red blood cell (RBC) deformability is a valuable hemorheological biomarker that can be used to assess the clinical status and response to therapy of individuals with sickle cell disease (SCD). RBC deformability has been measured by ektacytometry for decades, which uses shear or osmolar stress. However, ektacytometry is a population based measurement that does not detect small-fractions of abnormal RBCs. A single cell-based, functional RBC deformability assay would complement ektacytometry and provide additional information. Here, we tested the relative merits of the OcclusionChip, which measures RBC deformability by microcapillary occlusion, and ektacytometry. We tested samples containing glutaraldehyde-stiffened RBCs for up to 1% volume fraction; ektacytometry detected no significant change in Elongation Index (EI), while the OcclusionChip showed significant differences in Occlusion Index (OI). OcclusionChip detected a significant increase in OI in RBCs from an individual with sickle cell trait (SCT) and from a subject with SCD who received allogeneic hematopoietic stem cell transplant (HSCT), as the sample was taken from normoxic (pO2:159 mmHg) to physiologic hypoxic (pO2:45 mmHg) conditions. Oxygen gradient ektacytometry detected no difference in EI for SCT or HSCT. These results suggest that the single cell-based OcclusionChip enables detection of sickle hemoglobin (HbS)-related RBC abnormalities in SCT and SCD, particularly when the HbS level is low. We conclude that the OcclusionChip is complementary to the population based ektacytometry assays, and providing additional sensitivity and capacity to detect modest abnormalities in red cell function or small populations of abnormal red cells.
红细胞(RBC)变形性是一种有价值的血液流变学生物标志物,可用于评估镰状细胞病(SCD)患者的临床状况和对治疗的反应。几十年来,一直通过激光衍射血细胞分析法测量RBC变形性,该方法使用剪切力或渗透压。然而,激光衍射血细胞分析法是一种基于群体的测量方法,无法检测到小部分异常RBC。基于单细胞的功能性RBC变形性检测方法将补充激光衍射血细胞分析法,并提供额外信息。在此,我们测试了通过微毛细管阻塞测量RBC变形性的阻塞芯片与激光衍射血细胞分析法的相对优缺点。我们测试了含有高达1%体积分数的戊二醛硬化RBC的样本;激光衍射血细胞分析法未检测到伸长指数(EI)有显著变化,而阻塞芯片显示阻塞指数(OI)有显著差异。当样本从常氧(pO2:159 mmHg)条件采集到生理性低氧(pO2:45 mmHg)条件时,阻塞芯片检测到镰状细胞性状(SCT)个体和接受异基因造血干细胞移植(HSCT)的SCD患者的RBC中OI显著增加。氧梯度激光衍射血细胞分析法未检测到SCT或HSCT的EI有差异。这些结果表明,基于单细胞的阻塞芯片能够检测SCT和SCD中与镰状血红蛋白(HbS)相关的RBC异常,尤其是当HbS水平较低时。我们得出结论,阻塞芯片是基于群体的激光衍射血细胞分析法的补充,能够提供额外的灵敏度和能力来检测红细胞功能的适度异常或少量异常红细胞群体。