Endothelial progenitor cells (EPCs) have been implicated in vascular repair and found to be functionally impaired in patients with diabetes. We evaluated the effects of the anti-diabetic drug pioglitazone on human EPC function and the involvement of PPAR-gamma and TGF-beta1. EPCs in culture were characterized at day 7 by the development of colony-forming units (CFUs) and flow cytometry assessment of differentiation marker (DiI-ac-LDL/lectin, KDR and CD31). Adhesion on fibronectin and fibrinogen in flow was analyzed as functional parameter. Treatment with pioglitazone for 72 hours increased the number of EPC-CFUs, DiI-ac-LDL(+)/lectin(+), CD31(+) and KDR(+) EPCs at 1 microM but not at 10 microM. Since pioglitazone did not significantly alter proliferation and apoptosis in cultured EPCs, the increase in EPC number was most likely attributable to augmented adhesion and differentiation. Indeed, pioglitazone increased EPC adhesion in flow at 1 microM, an effect prevented by PPAR-gamma and beta2-integrin blockade. In contrast, pioglitazone did not promote EPC adhesion at 10 microM; however, increased adhesion became evident by co-incubation with a blocking TGF-beta1 antibody. As determined by ELISA, pioglitazone induced a persistent increase in TGF-beta1 secretion only at 10 microM when a significantly elevated expression of endoglin, the accessory receptor for TGF-beta1, was also observed. Taken together, pioglitazone exerts biphasic effects on the function of isolated EPCs, causing a PPAR-gamma-dependent stimulation at 1 microM and a TGF-beta1-mediated suppression at 10 microM. These results may help to define optimal therapeutic doses of pioglitazone for improving endothelial dysfunction.

译文

内皮祖细胞 (epc) 与血管修复有关,并发现糖尿病患者的功能受损。我们评估了抗糖尿病药物吡格列酮对人EPC功能的影响以及PPAR-γ 和TGF-beta1的参与。培养物中的epc在第7天通过集落形成单位 (CFUs) 的发育和分化标记物 (DiI-ac-LDL/凝集素,KDR和CD31) 的流式细胞仪评估来表征。分析了血流中纤连蛋白和纤维蛋白原的粘附作为功能参数。吡格列酮治疗72小时可增加EPC-cfu,DiI-ac-LDL ()/凝集素 (),CD31 () 和KDR () EPCs的数量,但在10微米时却没有。由于吡格列酮不会显着改变培养的EPC的增殖和凋亡,因此EPC数量的增加很可能归因于粘附和分化的增强。实际上,吡格列酮在1微米时增加了流动中的EPC粘附力,这是由PPAR-γ 和beta2-integrin阻断所阻止的。相反,吡格列酮在10微米时不促进EPC粘附; 然而,通过与阻断TGF-beta1抗体共孵育,增加的粘附变得明显。通过ELISA确定,当还观察到TGF-beta1的辅助受体endoglin的表达显着升高时,吡格列酮仅在10微米处诱导TGF-beta1分泌持续增加。合在一起,吡格列酮对分离的epc的功能发挥双相作用,在1微米处引起PPAR-γ 依赖性刺激,在10微米处引起TGF-beta1-mediated抑制。这些结果可能有助于确定吡格列酮改善内皮功能障碍的最佳治疗剂量。

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