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腐殖酸诱导培养的内皮细胞表达组织因子:由胞质钙和蛋白激酶C调控。

Humic acid induces expression of tissue factor by cultured endothelial cells: regulation by cytosolic calcium and protein kinase C.

作者信息

Yang H L, Lu F J, Wung S L, Chiu H C

机构信息

Institute of Biomedical Sciences, Academia Sinico, Taipei, Taiwan, R.O.C.

出版信息

Thromb Haemost. 1994 Mar;71(3):325-30.

PMID:8029797
Abstract

Blackfoot disease is a thrombotic peripheral vascular disease causally related to the fluorescent humic acid (HA) found in the drinking water of wells in endemic areas in Taiwan. In this study we examined the effect of HA on tissue factor (TF) expression by vascular endothelial cells. Incubation of cultured human umbilical vein endothelial cells (HUVEC) with HA isolated from endemic area drinking water or with a synthetic humic acid polymer (SHA), resulted in enhanced cell surface expression of TF activity by HUVEC. The intracellular calcium level ([Ca2+]i) was measured using a calcium-specific fluorescent probe, fura 2. Changes in [Ca2+]i level were followed and quantitatively analyzed by spectrofluorometric microscopy, after incubation of the fura 2-loaded HUVEC with HA or SHA in a medium containing 1.8 mM CaCl2. Both HA and SHA increased [Ca2+]i in the presence of extracellular calcium ions, but not in their absence, indicating that influx of extracellular Ca2+ occurred during incubation of HUVEC with HA or SHA. Verapamil, a potent calcium channel blocker, did not abolish the enhancement of [Ca2+]i induced by HA or SHA, indicating that specific calcium channels may not be involved in the HA/SHA-induced elevation of [Ca2+]i. The elevated [Ca2+]i level induced by HA or SHA returned to basal level following removal of HA or SHA and incubation of the washed cells in medium containing 1.8 mM CaCl2. All these changes occurred in the absence of significant cytotoxic effects.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

乌脚病是一种血栓性外周血管疾病,与台湾流行地区水井饮用水中发现的荧光腐殖酸(HA)存在因果关系。在本研究中,我们检测了HA对血管内皮细胞组织因子(TF)表达的影响。用从流行地区饮用水中分离出的HA或合成腐殖酸聚合物(SHA)培养人脐静脉内皮细胞(HUVEC),导致HUVEC细胞表面TF活性表达增强。使用钙特异性荧光探针fura 2测量细胞内钙水平([Ca2+]i)。在含有1.8 mM氯化钙的培养基中,将负载fura 2的HUVEC与HA或SHA孵育后,通过荧光光谱显微镜跟踪并定量分析[Ca2+]i水平的变化。HA和SHA在细胞外钙离子存在的情况下均增加了[Ca2+]i,但在其不存在时则没有,这表明在HUVEC与HA或SHA孵育期间发生了细胞外Ca2+的内流。强效钙通道阻滞剂维拉帕米并未消除HA或SHA诱导的[Ca2+]i增强,这表明特定的钙通道可能不参与HA/SHA诱导的[Ca2+]i升高。去除HA或SHA并将洗涤后的细胞在含有1.8 mM氯化钙的培养基中孵育后,HA或SHA诱导的升高的[Ca2+]i水平恢复到基础水平。所有这些变化均在无明显细胞毒性作用的情况下发生。(摘要截短至250字)

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