Increased expression of tissue factor and receptor for advanced glycation end products in peripheral blood mononuclear cells of patients with type 2 diabetes mellitus with vascular complications.

A E Buchs, A Kornberg, M Zahavi, D Aharoni, C Zarfati, M J Rapoport
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引用次数: 15

Abstract

The aim of the study was to determine the correlation between the expression of tissue factor (TF) and the receptor for advanced glycation end products (RAGEs) and vascular complications in patients with longstanding uncontrolled type 2 diabetes (T2D). TF and RAGE mRNAs as well as TF antigen and activity were investigated in 21 T2D patients with and without vascular complications. mRNA expression was assessed by reverse transcriptase-polymerase chain reaction (RT-PCR) in nonstimulated and advanced glycation end product (AGE) albumin-stimulated peripheral blood mononuclear cells (PBMCs). TF antigen expression was determined by enzyme-linked immunosorbent assay (ELISA) and TF activity by a modified prothrombin time assay. Basal RAGE mRNA expression was 0.2 +/- 0.06 in patients with complications and 0.05 +/- 0.06 patients without complications (P =.004). Stimulation did not cause any further increase in either group. TF mRNA was 0.58 +/- 0.29 in patients with complications and 0.21 +/- 0.18 in patients without complications (P =.003). Stimulation resulted in a nonsignificant increase in both groups. Basal TF activity (U/10(6) PBMCs) was 18.4 +/- 13.2 in patients with complications and 6.96 +/- 5.2 in patients without complications (P =.003). It increased 3-fold in both groups after stimulation (P =.001). TF antigen (pg/10(6) PBMCs) was 33.7 +/- 28.6 in patients with complications, 10.4 +/- 7.8 in patients without complications (P =.02). Stimulation tripled TF antigen in both groups of patients (P =.001). The RAGE/TF axis is up-regulated in T2D patients with vascular complications as compared to patients without complications. This suggests a role for this axis in the pathogenesis of vascular complications in T2D.

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2型糖尿病伴血管并发症患者外周血单个核细胞组织因子和晚期糖基化终产物受体的表达升高
该研究的目的是确定长期不受控制的2型糖尿病(T2D)患者中组织因子(TF)和晚期糖基化终产物(RAGEs)受体的表达与血管并发症之间的相关性。研究了21例合并和不合并血管并发症的T2D患者的TF和RAGE mrna以及TF抗原和活性。通过逆转录聚合酶链反应(RT-PCR)评估未刺激和晚期糖基化终产物(AGE)白蛋白刺激的外周血单个核细胞(PBMCs) mRNA表达。采用酶联免疫吸附法(ELISA)检测TF抗原表达,采用改良凝血酶原时间法检测TF活性。有并发症组RAGE mRNA基础表达量为0.2 +/- 0.06,无并发症组RAGE mRNA基础表达量为0.05 +/- 0.06 (P = 0.004)。刺激并没有引起任何进一步的增加。并发症组TF mRNA为0.58 +/- 0.29,无并发症组为0.21 +/- 0.18 (P = 0.003)。刺激在两组中都导致了不显著的增加。有并发症患者的基础TF活性(U/10(6) PBMCs)为18.4 +/- 13.2,无并发症患者为6.96 +/- 5.2 (P = 0.003)。两组经刺激后均增加3倍(P =.001)。并发症组TF抗原(pg/10(6) PBMCs)为33.7 +/- 28.6,无并发症组为10.4 +/- 7.8 (P = 0.02)。刺激使两组患者的TF抗原增加了两倍(P = 0.001)。与无并发症的T2D患者相比,有血管并发症的T2D患者RAGE/TF轴上调。这表明该轴在T2D血管并发症的发病机制中起作用。
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