循环内皮祖细胞在镰状细胞患者微血管损伤中的作用

B. Osa-Andrews, S. Oppong, H. Asare-Anane, G. Kpentey, T. John, B. Gyan
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摘要

血管壁参与镰状细胞病(SCD)的发病。循环内皮祖细胞(cEPCs)在SCD的血管病理中也起着关键作用,包括疼痛危机。在先前的研究中,在涉及血管损伤的情况下,如心肌梗死,发现cEPCs水平降低。本研究的目的是研究cEPCs在SCD血管病理中的作用。流式细胞术采用流式活化细胞分选机(FACS)对cEPCs进行计数。为了区分不同的基因型(ss、SC、AS、AC和AA),采用了Hb电泳。结果显示,SCD患者的中位数% cEPCs (CD34+/VEGF-2+)[0.555(0.4, 0.765)]低于健康对照组[1.08(0.87,1.39)(p=0.001)]。危重患者的cepc(0.65+0.39)高于稳定患者(0.59+0.28)(p=0.522)。SS组平均GGT最高(73.66+73.35)。在受试者中,只有总胆固醇与cepc呈正相关(r=0.378, p=0.00814);这一趋势在健康对照组中是看不到的。患者WBC、Hb及肝酶- ALT、GGT、ALP与cEPCs无相关性。而在健康对照中,白细胞与cepc呈负相关(r=-0.6293, p=0.0003)。SCD既是一种内皮功能障碍疾病,也是一种触发红细胞聚合的血红蛋白病:cEPC是SCD患者血管功能的替代生物标志物。结果表明,与健康对照相比,SCD患者的cEPCs减少。在归巢过程中,氧化应激、一氧化氮活性、CD133的丢失会影响祖细胞群。总胆固醇与cepc呈正相关。高总胆固醇可能预示着痛苦危机的开始。肝酶与cEPCs没有相关性,即使肝参与了SCD患者的内皮损伤。SS个体往往有较高的GGT。总的来说,我们已经证明了镰状细胞患者的总胆固醇和cEPCs之间的直接相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of Circulating Endothelial Progenitor Cells in Micro VascularDamage in Sickle Cell Patients
The vascular wall participates in the pathogenesis of sickle cell disease (SCD). Circulating Endothelial progenitor cells (cEPCs) also play a key role in the vascular pathology of SCD, including the painful crisis. In previous investigations, reduced levels of cEPCs were found in conditions in which vascular injury is implicated such as myocardial infarction. The aim of this research is to study the role of cEPCs in the vascular pathology of SCD. cEPCs were enumerated using flow cytometry with the Flow Activated Cell Sorting machine (FACS). To differentiate the various genotypes-SS, SC, AS, AC and AA, Hb Electrophoresis was employed. Results showed that the median % cEPCs (CD34+/VEGF-2+) was lower in patients with SCD [0.555(0.4, 0.765)] than in healthy controls [(1.08(0.87, 1.39) (p=0.001)]. Patients in crisis had a higher cEPCs (0.65+0.39) than those in steady state (0.59+0.28) (p=0.522). SS group recorded the highest mean GGT (73.66+73.35). Only total cholesterol demonstrated a positive correlation (r=0.378, p=0.00814) with cEPCs in subjects; a trend unseen in healthy controls. Patients’ WBC, Hb and Liver enzymes- ALT, GGT, ALP showed no correlation with cEPCs. In healthy controls though, WBCs showed an inverse correlation with cEPCs (r=-0.6293, p=0.0003). SCD is as much a disease of endothelial dysfunction as it is a hemoglobinopathy that triggers erythrocyte polymerization: cEPC is a surrogate bio-marker for vascular function in SCD patients. The results suggest that SCD patients have depleted cEPCs compared with healthy controls. Oxidative stress, Nitric oxide activity, loss of CD133 during homing could influence progenitor cell populations. Total cholesterol positively correlates with cEPCs. High total cholesterol could spell the onset of painful crisis. Liver enzymes are not related to cEPCs correlatively even though the liver is involved in endothelial injury in SCD patients. SS individuals tend to have a high GGT. Overall, we have shown the direct correlation between total cholesterol and cEPCs in sickle cell patients.
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