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首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >FMLP-, thapsigargin-, and H2O2-evoked changes in intracellular free calcium concentration in lymphocytes and neutrophils of type 2 diabetic patients
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FMLP-, thapsigargin-, and H2O2-evoked changes in intracellular free calcium concentration in lymphocytes and neutrophils of type 2 diabetic patients

机译:FMLP,毒胡萝卜素和H2O2引起2型糖尿病患者淋巴细胞和中性粒细胞的细胞内游离钙浓度变化

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摘要

Type 2 diabetic (T2DM) patients are immune-compromised having a higher susceptibility to infections and long-term complications in different parts of the body contributing to increased morbidity and mortality. A derangement in the homeostasis of intracellular free calcium concentration [Ca2+] i is known to be associated with several diseases in the body including T2DM. Both neutrophils and lymphocytes play active protective roles in host immune response to infection showing impairment in microbicidal functions including phagocytosis and chemotaxis which are calcium-dependent processes. This study evaluated the process of [Ca2+]i mobilization from both neutrophils and lymphocytes taken from blood of both T2DM patients and healthy age-matched control subjects investigating the effect of N-formyl-methionyl-leucyl-phenylalanine (fMLP), thapsigargin (TG), and hydrogen peroxide (H2O2) on [Ca2+]i homeostasis. This study employed isolated peripheral blood neutrophils and lymphocytes from 24 T2DM patients and 24 healthy volunteers. Either neutrophils or lymphocytes were stimulated separately with fMLP, TG, or H2O 2. Induced changes in [Ca2+] in both neutrophils and lymphocytes were evaluated using spectrofluorometric methods. Stimulation of human neutrophils and lymphocytes with fMLP, TG, or H2O2 in the presence of [Ca2+]o resulted in significant decreases in [Ca2+]i mobilization from T2DM patients compared with healthy controls. These data indicate that neutrophils and lymphocytes from T2DM patients are less responsive to calcium mobilizing agents compared with granulocytes from healthy controls and this is possibly due to the hyperglycemia. The results suggest that agonist-evoked decrease in [Ca 2+]i in immune cells might be one of the possible mechanisms of impaired immunity in diabetic patients.
机译:2型糖尿病(T2DM)患者免疫受损,对身体不同部位的感染和长期并发症的敏感性更高,从而导致发病率和死亡率增加。已知细胞内游离钙浓度[Ca 2+] i的稳态紊乱与包括T2DM在内的多种疾病有关。中性粒细胞和淋巴细胞在宿主对感染的免疫反应中均发挥积极的保护作用,显示出包括钙依赖性过程的吞噬作用和趋化作用在内的杀微生物功能受损。这项研究评估了T2DM患者和年龄匹配的健康对照者血液中嗜中性粒细胞和淋巴细胞的[Ca2 +] i动员过程,研究了N-甲酰基-甲硫酰基-亮氨酰-苯丙氨酸(fMLP),毒胡萝卜素(TG)的作用)和过氧化氢(H2O2)对[Ca2 +] i的体内平衡。这项研究采用了来自24名T2DM患者和24名健康志愿者的分离的外周血中性粒细胞和淋巴细胞。用fMLP,TG或H2O分别刺激中性粒细胞或淋巴细胞。使用分光荧光法评估中性粒细胞和淋巴细胞中[Ca2 +]的诱导变化。与健康对照组相比,在[Ca2 +] o存在下用fMLP,TG或H2O2刺激人中性粒细胞和淋巴细胞导致T2DM患者的[Ca2 +] i动员显着降低。这些数据表明,与健康对照组的粒细胞相比,T2DM患者的中性粒细胞和淋巴细胞对钙动员的反应较弱,这可能是由于高血糖引起的。结果表明,激动剂引起的免疫细胞中[Ca 2+] i减少可能是糖尿病患者免疫功能受损的可能机制之一。

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