Serum from patients with erectile dysfunction inhibits circulating angiogenic cells from healthy men: relationship with cardiovascular risk, endothelial damage and circulating angiogenic modulators

F. Pelliccione, A. D’Angeli, S. Filipponi, S. Falone, S. Necozione, A. Barbonetti, F. Francavilla, S. Francavilla
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引用次数: 13

Abstract

Erectile dysfunction (ED) is an early manifestation of arteriosclerosis associated with endothelial damage/dysfunction and to a blunted ability of cultured mononuclear circulating cells (MNCs) to differentiate circulating angiogenic cells (CACs), putatively involved in endothelial damage repair. Here we explored effects of human serum (HS) from patients with ED and cardiovascular risk factors (VRFs) but no clinical atherosclerosis, on cultured MNCs of healthy men to differentiate CACs and to form colonies. Effect of HS on number of CACS and of colony forming units (CFUs) was correlated with circulating markers of endothelial damage and with angiogenic modulators. MNCs from healthy men were cultured in standard conditions or with 20% HS from 35 patients with ED and from 10 healthy men. CACs were identified after 7 days of culture by uptake of acetylated low-density lipoprotein with concomitant binding of Ulex europaeus agglutinin I. CFUs were counted after 5 days of culture. Enzyme-linked immunosorbent assays assessed plasmatic soluble (s) form of E-selectin, Endothelin (ET)-1, tissue type plasminogen activator (tPA), vascular endothelial growth factor (VEGF)165 and sVEGF receptor (R)-1. The number of CACs and of CFUs from healthy men was reduced after culturing MNCs with HS compared to standard medium. The inhibitory effect was significantly higher with HS from ED patients with higher or lower VRF exposure compared to healthy men. Inhibition was positively correlated with VRFs exposure, with ED severity, with common carotid artery intima media thickness measured using B-mode ultrasound, and to a lesser extent with plasmatic sE-Selectin, sET-1 and sVEGFR-1. Dysfunction of cells involved in vascular homoeostasis is induced by soluble factors still unknown and already present in a very initial systemic vascular disease in men with ED and VRFs.

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勃起功能障碍患者血清抑制健康男性循环血管生成细胞:与心血管风险、内皮损伤和循环血管生成调节剂的关系
勃起功能障碍(ED)是动脉硬化的早期表现,与内皮损伤/功能障碍和培养的单核循环细胞(MNCs)分化循环血管生成细胞(CACs)的能力减弱有关,据推测,循环血管生成细胞参与内皮损伤修复。在这里,我们探讨了来自ED和心血管危险因素(vrf)但无临床动脉粥样硬化患者的人血清(HS)对培养的健康男性MNCs分化cac和形成菌落的影响。HS对CACS和菌落形成单位(cfu)数量的影响与循环内皮损伤标志物和血管生成调节剂有关。35例ED患者和10例健康男性的MNCs分别在标准条件下或20% HS中培养。在培养7天后,通过摄取乙酰化低密度脂蛋白并结合欧洲巨藻凝集素i来鉴定ccs。酶联免疫吸附试验评估血浆可溶性e-选择素、内皮素(ET)-1、组织型纤溶酶原激活剂(tPA)、血管内皮生长因子(VEGF)165和sVEGF受体(R)-1。与标准培养基相比,用HS培养MNCs后,健康男性的cac和cfu数量减少。与健康男性相比,VRF暴露较高或较低的ED患者的HS抑制作用明显更高。抑制作用与vrf暴露、ED严重程度、b超测量颈总动脉内膜中膜厚度呈正相关,与血浆se -选择素、sET-1和sVEGFR-1呈正相关。参与血管平衡的细胞功能障碍是由可溶性因子引起的,这些因子尚不清楚,但在ED和vrf患者的非常初始的系统性血管疾病中已经存在。
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6-12 weeks
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Goodbye International Journal of Andrology, welcome Andrology! Progesterone and CatSper dependency Novel mutations in calcium/calmodulin-dependent protein kinase IV (CAMK4) gene in infertile men Variations in testosterone pathway genes and susceptibility to testicular cancer in Norwegian men Selective resection of dorsal nerves of penis for premature ejaculation
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