采用新型的基于电阻抗的微流控装置评估红细胞介导的雀斑细胞疾病微血管闭塞

ty10086 提交于 周三, 08/25/2021 - 16:40
文章英文标题
Assessment of Red Blood Cell-Mediated Microvascular Occlusion in Sickle Cell Disease By a Novel Electrical Impedance-Based Microfluidic Device
正文
导言:镰状细胞病( SCD )是由红细胞中的镰状血红蛋白( HbS )突变引起的隐性遗传性疾病,HbS在缺氧环境中聚合,导致红细胞粘附性增强,变形能力下降,最终导致SCD微血管闭塞。由于红细胞变形性和相关的微血管阻塞是个体微循环健康的预测因素,以往的研究开发了基于红细胞变形性的微流控分选装置,但其通量相对较低。快速评估红细胞介导的微血管闭塞的简便、易行的临床经验可用于检测抗晕厥药物和基因治疗等新型靶向治疗对SCD患者的疗效。在此,我们提出了一种基于电阻抗的微流控装置和功能评估红细胞介导的微血管闭塞在SCD。\n方法:在IRB批准的协议下,在EDTA中采集纯合SCD ( HbSS,N = 12 )和对照( HbAA,N = 5 )受试者的静脉血标本。采用标准光刻和聚二甲基硅氧烷( PDMS )微成型工艺制备了微流控器件。微通道由微柱阵列组成,从3 ~ 12μm形成微柱体,每个阵列在通道底面耦合一对金电极(图1A )。设计了两个40μm宽的模拟毛细管床内吻合口的侧通道,以防止微通道上游堵塞(图1A插图)。设备的宏观视图如图1B所示。12μm阵列用于过滤大细胞聚集体,被排除在我们的分析之外。采用阻抗分析仪与自定义印制电路板耦合,在10kHz的点频下记录电阻抗。实验前,对微通道进行堵塞和冲洗,防止血细胞非特异性黏附。然后,得到各阵列的初始电阻抗读数。将悬浮于PBS中红细胞压积20 %的红细胞,在相同入口压力下通过微通道灌注20 min。然后对微通道进行清洗,得到二次电阻抗读数。然后在倒置显微镜下对微通道进行成像,手动量化每个阵列的遮挡情况。电阻抗和遮挡的结果报告为百分之百的变化。数据以均数±标准差( SD )表示,采用Pearson’s相关系数( PCC )推导相关统计量。\n结果:HbSS - vs . HbAA诱导的红细胞微管闭塞率增加(图1C,3 μ m组平均微管闭塞率± SD ( % ) = 24.33 ± 16.88 vs . 5.01 ± 1.25,4 μ m组6.05 ± 4.09 vs . 2.19 ± 0.59,6 μ m组2.77 ± 2.59 vs . 0.82 ± 0.82,8 μ m组1.08 ± 2.28 vs . 0 ± 0,10 μ m组0.42 ± 1.14 vs . 0 ± 0 )。同样,我们观察到HbSS - vs . HbAA诱导的红细胞电阻抗变化(图1D,3 - μ m阵列平均电阻抗变化± SD ( % ) = 12.03 ± 8.97 vs . 2.44 ± 0.84,4 - μ m阵列平均电阻抗变化1.79 ± 1.65 vs . 0.91 ± 0.42,6 - μ m阵列平均电阻抗变化0.88 ± 1.14 vs . 0.58 ± 0.67,8 - μ m阵列平均电阻抗变化0.16 ± 0.31 vs . 0.32 ± 0.37,10 - μ m阵列平均电阻抗变化0.06 ± 0.16 vs . 0.05 ± 0.17 )。此外,我们还发现,单个阵列的电阻抗变化与对应阵列内部的遮挡百分比显著相关(图1E,PCC = 0.9817,N = 85,p )
文章内容(英文)
Introduction: Sickle cell disease (SCD) is a recessive genetic disorder caused by the mutated sickle hemoglobin (HbS) in red blood cells (RBCs). HbS polymerizes in a hypoxic environment, which leads to increased adhesiveness and decreased deformability of RBCs, and ultimately contributes to microvascular occlusion in SCD. As RBC deformability and the associated microvascular occlusion are predictors of individual microcirculatory health, previous studies have developed microfluidic devices for deformability-based RBC sorting in microscale flow, albeit with relatively low throughput. An easy-to-use, point-of-care assay to rapidly assess RBC-mediated microvascular occlusion can be clinically useful in examining the outcome of novel targeted and curative therapies, such as anti-sickling drugs and gene therapies, for patients with SCD. Here, we present an electrical impedance-based microfluidic device and functional assessment of RBC-mediated microvascular occlusion in SCD.(#br)Methods: Venous blood samples were collected in EDTA from subjects with homozygous SCD (HbSS, N=12) and controls (HbAA, N=5) under consent in an IRB-approved protocol. Microfluidic devices were fabricated using standard photolithography and polydimethylsiloxane (PDMS) micro-molding protocols. The microchannel consisted of micropillar arrays forming microcapillaries from 3-12 μm, with each array coupled with a pair of gold electrodes on the channel bottom surface (Figure 1A). Two 40-μm-wide side passageways mimicking the anastomoses in the capillary bed were designed to prevent microchannel upstream clogging (Figure 1A inset). A macroscopic view of the device is shown in Figure 1B. The 12-μm array was designed to filter large-cell aggregates and was excluded from our analysis. An impedance analyzer coupled with a custom printed-circuit board was used to record the electrical impedance at a spot frequency of 10 kHz. Prior to the experiments, the microchannel was blocked and rinsed to prevent non-specific adhesion of blood cells. Thereafter, the initial electrical impedance reading of each array was obtained. RBCs suspended at 20% hematocrit in PBS were then perfused through the microchannel under the same inlet pressure for 20 min. Next, the microchannel was washed and a second electrical impedance reading was obtained. The microchannel was then imaged under an inverted microscope, and occlusions of each array were manually quantified. The electrical impedance and occlusion results are reported as percent changes. Data are reported as mean ± standard deviation (SD). Pearson’s correlation coefficient (PCC) was used to derive correlation statistics.(#br)Results: We observed increased microcapillary occlusion caused by HbSS- vs. HbAA-containing RBCs (Figure 1C, mean microcapillary occlusion percentage ± SD (%) = 24.33 ± 16.88 vs. 5.01 ± 1.25 for 3-μm array, 6.05 ± 4.09 vs. 2.19 ± 0.59 for 4-μm array, 2.77 ± 2.59 vs. 0.82 ± 0.82 for 6-μm array, 1.08 ± 2.28 vs. 0 ± 0 for 8-μm array, and 0.42 ± 1.14 vs. 0 ± 0 for 10-μm array). Similarly, we observed elevated electrical impedance change induced by HbSS- vs. HbAA-containing RBCs (Figure 1D, mean electrical impedance change ± SD (%) = 12.03 ± 8.97 vs. 2.44 ± 0.84 for 3-μm array, 1.79 ± 1.65 vs. 0.91 ± 0.42 for 4-μm array, 0.88 ± 1.14 vs. 0.58 ± 0.67 for 6-μm array, 0.16 ± 0.31 vs. 0.32 ± 0.37 for 8-μm array, and 0.06 ± 0.16 vs. 0.05 ± 0.17 for 10-μm array). Moreover, we found that the electrical impedance changes of individual arrays exhibited a significant correlation to the occlusion percentage within the corresponding arrays (Figure 1E, PCC = 0.9817, N = 85, p \u0026lt; 0.001).(#br)Conclusions: Findings suggest that a novel microfluidic platform integrated with micropillar arrays and electrical impedance readout can be used for standardized in vitro functional assessment of RBC-mediated microvascular occlusion in SCD. Electrical impedance change due to RBC-mediated microcapillary occlusion may serve as a new parameter for monitoring RBC health and function without the need for high-resolution microscopic imaging. RBC mediated microcapillary occlusion may serve as a new parameter to assess the clinical efficacy of treatments that improve RBC deformability and rheology, such as hemoglobin modifying drugs, anti-sickling agents, and therapies with curative intent.(#br) [Display omitted] (#br)Disclosures(#br)Maji:Xatek Inc.: Patents \u0026amp; Royalties. An:Hemex Health, Inc.: Patents \u0026amp; Royalties. Ahuja:Genentech: Consultancy, Honoraria; Sanofi Genzyme: Consultancy, Honoraria; XaTek, Inc.: Consultancy, Patents \u0026amp; Royalties, Research Funding. Little:BioChip Labs: Patents \u0026amp; Royalties: SCD Biochip (patent, no royalties); Hemex Health, Inc.: Patents \u0026amp; Royalties: Microfluidic electropheresis (patent, no royalties); Bluebird Bio: Research Funding; GBT: Research Funding; GBT: Membership on an entity’s Board of Directors or advisory committees; NHLBI: Research Funding. Mohseni:Xatek Inc.: Consultancy, Patents \u0026amp; Royalties, Research Funding. Suster:Xatek Inc.: Consultancy, Patents \u0026amp; Royalties, Research Funding. Gurkan:BioChip Labs: Patents \u0026amp; Royalties; Xatek Inc.: Patents \u0026amp; Royalties; Dx Now Inc.: Patents \u0026amp; Royalties; Hemex Health, Inc.: Consultancy, Current Employment, Patents \u0026amp; Royalties, Research Funding.
来源出处
Journal|[J]BloodVolume 136, Issue S1. 2020. PP 10-10
DOI
https://doi.org/10.1182/BLOOD-2020-138876

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