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阿利吉仑直接改善 II 型糖尿病患者的内皮祖细胞功能。

Aliskiren directly improves endothelial progenitor cell function from Type II diabetic patients.

机构信息

Institute of Pharmacology, National Yang-Ming University, Taipei, Taiwan.

Department of Medicine, Taipei Veterans General Hospital, Taipei, Taiwan.

出版信息

Eur J Clin Invest. 2016 Jun;46(6):544-54. doi: 10.1111/eci.12632. Epub 2016 Apr 30.

DOI:10.1111/eci.12632
PMID:27062013
Abstract

BACKGROUND

Endothelial progenitor cell (EPC) functions are impaired in the presence of diabetes mellitus. Aliskiren is a direct renin inhibitor, which is expected to modify proangiogenic cells. This study aimed to investigate whether and how aliskiren could improve the function of EPCs from patients with type II diabetes (T2DM).

MATERIALS AND METHODS

Endothelial progenitor cells fibronectin adhesion assay, chamber assay and in vitro tube formation assay were used to estimate the degree of EPC adhesion, migration and tube formation abilities. EPC protein and mRNA expressions were evaluated by Western blot and quantitative RT-PCR, respectively. EPC vascular endothelial growth factor (VEGF) and (pro)renin receptor ((P)RR) expression was knocked down by VEGF and (P)RR siRNA.

RESULTS

Aliskiren (0·1 or 10 μM) dose-dependently improved functions and increased both VEGF and stromal cell-derived factor-1α (SDF-1α) expression of EPCs from patients with T2DM or EPCs from healthy volunteers and treated with high glucose. Transfection with VEGF siRNA significantly reduced the aliskiren-induced SDF-1α expression. Furthermore, (P)RR siRNA transfection impaired the aliskiren-induced VEGF and SDF-1 expression.

CONCLUSIONS

The results show that aliskiren improved EPC function from patients with T2DM in a dose-dependent manner probably via the (P)RR and VEGF/SDF-1α-related mechanisms.

摘要

背景

内皮祖细胞(EPC)的功能在糖尿病患者中受损。阿利克仑是一种直接肾素抑制剂,预计可以修饰促血管生成细胞。本研究旨在探讨阿利克仑是否以及如何改善 2 型糖尿病(T2DM)患者的 EPC 功能。

材料和方法

采用内皮祖细胞纤维连接蛋白黏附试验、室试验和体外管形成试验来评估 EPC 黏附、迁移和管形成能力的程度。通过 Western blot 和定量 RT-PCR 分别评估 EPC 蛋白和 mRNA 的表达。通过 VEGF 和(P)RR siRNA 敲低 EPC 血管内皮生长因子(VEGF)和(前)肾素受体((P)RR)的表达。

结果

阿利克仑(0.1 或 10 μM)呈剂量依赖性地改善了来自 T2DM 患者或来自健康志愿者且经高葡萄糖处理的 EPC 的功能,并增加了 VEGF 和基质细胞衍生因子-1α(SDF-1α)的表达。VEGF siRNA 转染显著降低了阿利克仑诱导的 SDF-1α表达。此外,(P)RR siRNA 转染损害了阿利克仑诱导的 VEGF 和 SDF-1 表达。

结论

结果表明,阿利克仑以剂量依赖的方式改善了 T2DM 患者的 EPC 功能,可能通过(P)RR 和 VEGF/SDF-1α 相关机制。

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MiR-92a regulates endothelial progenitor cells (EPCs) by targeting GDF11 via activate SMAD2/3/FAK/Akt/eNOS pathway.
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