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Amelioration of Glucose Control Mobilizes Circulating Pericyte Progenitor Cells in Type 2 Diabetic Patients with Microangiopathy

机译:葡萄糖控制的改善动员2型糖尿病微血管病患者的循环周细胞祖细胞。

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摘要

Chronic diabetic complications result from an imbalance between vascular damage and regeneration. Several circulating lineage-committed progenitor cells have been implicated, but no data are available on pericyte progenitor cells (PPCs). Based on the evidence that PPCs increase in cancer patients after chemotherapy, we explored whether circulating PPC levels are affected by glucose control in type 2 diabetic patients, in relation to the presence of chronic complications. We enumerated peripheral blood PPCs as Syto16+CD45−CD31−CD140b+ events by flow cytometry at baseline and after 3 and 6 months of glucose control by means of add-on basal insulin therapy on top of oral agents in 38 poorly controlled type 2 diabetic patients. We found that, in patients with microangiopathy (n = 23), the level of circulating PPCs increased about 2 fold after 3 months and then returned to baseline at 6 months. In patients without microangiopathy (control group, n = 15), PPCs remained fairly stable during the whole study period. No relationship was found between change in PPCs and macroangiopathy (either peripheral, coronary, or cerebrovascular). We conclude that glucose control transiently mobilizes PPCs diabetic patients with microangiopathy. Increase in PPCs may represent a vasoregenerative event or may be a consequence of ameliorated glucose control on microvascular lesions.
机译:慢性糖尿病并发症是由血管损伤和再生之间的不平衡引起的。已经牵涉到几个循环世系的祖细胞,但是没有关于周细胞祖细胞(PPC)的数据。基于癌症患者化疗后PPC增加的证据,我们探讨了与慢性并发症的存在相关的2型糖尿病患者中循环PPC水平是否受血糖控制。我们通过流式细胞术在38例控制不好的2型糖尿病患者中,在基线时以及在口服药物的基础上通过附加基础胰岛素治疗对葡萄糖进行控制3、6个月后,通过流式细胞术将外周血PPC计数为Syto16 + CD45-CD31-CD140b +事件。 。我们发现,在微血管病患者(n = 23)中,循环中的PPC水平在3个月后增加了约2倍,然后在6个月时恢复到基线。在无微血管病的患者中(对照组,n = 15),PPC在整个研究期间保持相当稳定。在PPC的变化与大血管病变(外周,冠状动脉或脑血管)之间没有发现相关性。我们得出的结论是,葡萄糖控制可暂时动员患有微血管病的PPC糖尿病患者。 PPC的增加可能代表血管再生事件或可能是微血管病变上葡萄糖控制改善的结果。

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