Haemostasis Thrombosis and Vascular Biology Unit, University of Birmingham Centre for Cardiovascular Sciences, City Hospital, Birmingham B18 7QH, UK.
Thromb Haemost. 2010 Feb;103(2):419-25. doi: 10.1160/TH09-06-0386. Epub 2009 Nov 13.
Endothelial damage/dysfunction is involved in numerous cardiovascular disease processes. Given that the mature endothelial cells have limited capacity for self regeneration, circulating progenitor cells (CPCs) may modulate the balance between vascular damage and regeneration. The three aims of the present study were 1) to define the influence of exercise treadmill testing (ETT) on peripheral CPC levels; 2) to assess the diurnal variation of CPC counts; and 3) to investigate the rate of temporal decline in CPCs once ex vivo . The dynamics of CPC count changes following an ETT were assessed on consecutive 20 patients referred to our 'rapid-access' chest pain clinic (70% male, age 69.9 +/- 7.8) with venous blood samples taken pre-exercise, immediately post-exercise and at 30 minutes post-exercise. Diurnal variation in CPCs was assessed in 13 stable in-hospital patients (46% male, age 69.1 +/- 7.5 years) with blood samples were taken five times every 6 hours. To investigate the temporal decline, blood samples from 12 patients (58.3% male, age 69.9 +/- 7.9 years) were reprocessed for CPC counts at 4 hours and at 24 hours after sample collection. Plasma levels of von Willebrand factor (vWf) and soluble E-selectin (sE-selectin) were assessed by ELISA. CPCs were enumerated with flow cytometry as CD34+, CD133+, CD45dim events. Exercise led to significant increases in vWF and sE-selectin levels, but no significant influence on CPC counts were observed. Baseline CPC numbers demonstrated a negative correlation with vWf (r=-0.551, p=0.012) and sE-selectin levels (r=-0.494, p=0.027). CPC counts showed a significant diurnal variation, being significantly higher at 12 a.m. compared to 12 p.m. (p=0.046) and 6 p.m. (p=0.023). A 4 hour delay in sample preparation did not affect CPCs counts, but there was a significant decline in CPC recovery when sample processing was delayed by 24 hours (p<0.05). Routine exercise stress testing does not significantly affect CPC counts. Peripheral CPC levels showed a significant diurnal variation. Delays in sample preparation for CPC counts should be avoided as they may influence the accuracy of the test by resulting in a significant decline in CPC recovery. Thus, various factors may affect accuracy of CPC enumeration that may limit their role as a reliable clinical marker and biomarker of endothelial damage.
内皮细胞损伤/功能障碍与许多心血管疾病过程有关。鉴于成熟的内皮细胞自我再生能力有限,循环祖细胞(CPCs)可能调节血管损伤和再生之间的平衡。本研究的三个目的是:1)定义运动平板测试(ETT)对周围 CPC 水平的影响;2)评估 CPC 计数的昼夜变化;3)研究 CPC 一旦离体后时间下降的速度。对连续 20 名因胸痛而就诊于我们“快速通道”胸痛诊所的患者(70%为男性,年龄 69.9±7.8 岁)进行 ETT 后 CPC 计数变化的动力学评估,静脉血样本分别在运动前、运动后即刻和运动后 30 分钟采集。对 13 名稳定住院患者(46%为男性,年龄 69.1±7.5 岁)进行 CPC 的昼夜变化评估,每隔 6 小时采集 5 次血样。为了研究时间下降,对 12 名患者(58.3%为男性,年龄 69.9±7.9 岁)的血样进行 CPC 计数,分别在采集后 4 小时和 24 小时进行。通过 ELISA 评估 von Willebrand 因子(vWF)和可溶性 E-选择素(sE-选择素)的水平。通过流式细胞术将 CD34+、CD133+、CD45dim 事件作为 CPC 进行计数。运动导致 vWF 和 sE-选择素水平显著升高,但对 CPC 计数没有显著影响。基线 CPC 数量与 vWF(r=-0.551,p=0.012)和 sE-选择素水平(r=-0.494,p=0.027)呈负相关。CPC 计数存在明显的昼夜变化,与午夜相比,中午 12 点(p=0.046)和下午 6 点(p=0.023)的 CPC 计数明显更高。样本制备延迟 4 小时不会影响 CPC 计数,但如果将样本处理延迟 24 小时,CPC 恢复的显著下降(p<0.05)。常规运动应激测试对 CPC 计数没有显著影响。外周 CPC 水平存在明显的昼夜变化。应避免因 CPC 计数而延迟样本制备,因为这可能导致 CPC 恢复的显著下降,从而影响测试的准确性。因此,各种因素可能会影响 CPC 计数的准确性,这可能会限制它们作为内皮损伤可靠的临床标志物和生物标志物的作用。