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钙离子浓度变化动力学:来自糖尿病患者的中性粒细胞信号转导及其对胰岛素的影响。

Kinetics of calcium ion concentration accompanying transduction of signals into neutrophils from diabetic patients and its modification by insulin.

机构信息

Department of Laboratory Diagnostics and Clinical Immunology of Developmental Age, Warsaw Medical University, Warsaw, Poland.

出版信息

J Physiol Pharmacol. 2009 Nov;60 Suppl 5:37-40.

Abstract

The goal of the study was to evaluate the process of Ca(2+)-mediated transduction of signals into neutrophils from patients with type I diabetes and its modification by insulin. The study was performed with the use of isolated peripheral blood neutrophils from 20 diabetic patients and 30 healthy volunteers. Isolated granulocytes were stimulated separately by fMLP or insulin, or by both substances added to the medium in combinations: fMLP + insulin (after 20 min) or insulin + fMLP (after 20 min). fMLP evoked fast intracellular increase of free Ca(2+) concentration in neutrophils compared with the resting state (P<0.001). Similarly, the peak of fluorescence, as measured by Fluo 3 to Fura Red ratio, was significantly higher in neutrophils stimulated by insulin. Insulin did not cause any changes in intracellular Ca(2+) level when it was added to the previously fMLP-stimulated cells. Prestimulation with insulin significantly decreased fMLP-induced intracellular free Ca(2+) concentration, expressed as Fluo3/Fura Red ratio compared with fMLP alone (1.77 +/- 0.6 vs. 2.63 +/- 0.8, P<0.001). No relation between initial intracellular Ca(2+) in the resting state and the response to insulin was found. Nor was the response to fMLP alone related to intracellular Ca(2+) before stimulation. A strong correlation was observed between initial intracellular Ca(2+) after incubation with insulin and the response to fMLP (r=0.90, P<0.0001). In diabetic granulocytes, the intracellular Ca(2+) was significantly lower than in those from healthy donors in unstimulated cells (P<0.001), after fMLP stimulation (P<0.0001), in medium enriched by insulin (P<0.05), and after fMLP stimulation in insulin rich medium (P<0.001). Only in fMLP prestimulated samples, the emission of light did not differ after stimulation with insulin in granulocytes from both diabetic and healthy subjects. In conclusion, patients with type I diabetes have decreased levels of cytosolic Ca(2+) after insulin and fMLP stimulation in polymorphonuclear granulocytes. This abnormality is probably primarily responsible for the impaired neutrophilic function seen in these patients.

摘要

研究目的在于评估 1 型糖尿病患者中性粒细胞中 Ca(2+)-介导的信号转导过程,并研究胰岛素对此过程的影响。该研究采用分离的 20 名糖尿病患者和 30 名健康志愿者的外周血中性粒细胞进行。单独用 fMLP 或胰岛素或两种物质以不同组合(fMLP+胰岛素[20 分钟后]或胰岛素+fMLP[20 分钟后])刺激分离的嗜中性粒细胞。与静息状态相比,fMLP 快速诱发中性粒细胞胞内游离 Ca(2+)浓度的增加(P<0.001)。同样,用 Fluo 3 到 Fura Red 比率测量的荧光峰在胰岛素刺激的中性粒细胞中也明显更高。当胰岛素加入先前用 fMLP 刺激的细胞时,不会引起细胞内 Ca(2+)水平的任何变化。与单独用 fMLP 刺激相比,用胰岛素预刺激显著降低了 fMLP 诱导的细胞内游离 Ca(2+)浓度,表现为 Fluo3/Fura Red 比值(1.77 +/- 0.6 对 2.63 +/- 0.8,P<0.001)。未发现静息状态下初始细胞内 Ca(2+)与对胰岛素的反应之间存在任何关系。也未发现单独用 fMLP 刺激时的反应与刺激前的细胞内 Ca(2+)有关。观察到孵育胰岛素后初始细胞内 Ca(2+)与对 fMLP 的反应之间存在很强的相关性(r=0.90,P<0.0001)。在糖尿病粒细胞中,与健康供体相比,未刺激细胞(P<0.001)、fMLP 刺激后(P<0.0001)、胰岛素丰富培养基中(P<0.05)以及胰岛素丰富培养基中 fMLP 刺激后(P<0.001)的细胞内 Ca(2+)明显较低。只有在 fMLP 预刺激的样本中,胰岛素刺激后,糖尿病和健康受试者的粒细胞的光发射没有差异。总之,1 型糖尿病患者的多形核粒细胞在胰岛素和 fMLP 刺激后细胞浆 Ca(2+)水平降低。这种异常可能主要导致这些患者中性粒细胞功能受损。

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