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2,3,7,8-四氯二苯并对二恶英(TCDD)植入SCID小鼠后对人胸腺的毒性作用。

Toxicity of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) to the human thymus after implantation in SCID mice.

作者信息

de Heer C, Schuurman H J, Liem A K, Penninks A H, Vos J G, van Loveren H

机构信息

Laboratory for Pathology, National Institute of Public Health and Environmental Protection, Bilthoven, The Netherlands.

出版信息

Toxicol Appl Pharmacol. 1995 Oct;134(2):296-304. doi: 10.1006/taap.1995.1195.

Abstract

There are conflicting data with regard to the sensitivity of the human immune system to the toxic action of the highly toxic environmental pollutant 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). SCID mice engrafted with human fetal thymus and liver tissue fragments (SCID-hu mice), which sustain normal human T cell differentiation in the thymus graft, were used to directly assess the sensitivity of the human thymus for TCDD. Wistar rats and SCID-hu mice were exposed to 1, 5 or 25 micrograms TCDD/kg body weight. Histopathologic effects were evaluated for rat thymus and transplanted human thymus on Day 4 after exposure. The relative size of the cortex showed a dose-dependent decrease in both the normal rat thymus and grafted human thymus (significant at 25 micrograms/kg). SCID-ra mice (SCID mice with a fetal rat thymus and liver graft) were used as an intermediate model between the normal rat and SCID-hu mice, and were exposed to the same dose levels of TCDD. However, 90% of the SCID-ra mice developed a cutaneous graft-versus-host reaction, associated with lymphodepletion of the rat thymus grafts, and hence a limited number of SCID-ra mice were available for evaluation of TCDD effects. The data obtained in SCID-ra mice were in line with those in normal rat and grafted human thymus. In gas chromatography/mass spectrometry analysis, TCDD tissue concentrations in the normal rat thymus and grafted human thymus were similar. We conclude that the human thymus serves as a target for TCDD, and that the human thymus and the Wistar rat thymus display a comparable sensitivity to the toxic action of TCDD.

摘要

关于人类免疫系统对剧毒环境污染物2,3,7,8-四氯二苯并对二恶英(TCDD)毒性作用的敏感性,存在相互矛盾的数据。植入人胎儿胸腺和肝组织片段的重症联合免疫缺陷小鼠(SCID-hu小鼠),其胸腺移植物中维持正常的人类T细胞分化,被用于直接评估人类胸腺对TCDD的敏感性。将Wistar大鼠和SCID-hu小鼠暴露于1、5或25微克TCDD/千克体重。在暴露后第4天评估大鼠胸腺和移植的人类胸腺的组织病理学效应。在正常大鼠胸腺和移植的人类胸腺中,皮质的相对大小均呈现剂量依赖性减小(在25微克/千克时显著)。重症联合免疫缺陷-大鼠小鼠(植入胎儿大鼠胸腺和肝移植物的SCID小鼠)被用作正常大鼠和SCID-hu小鼠之间的中间模型,并暴露于相同剂量水平的TCDD。然而,90%的重症联合免疫缺陷-大鼠小鼠发生了皮肤移植物抗宿主反应,伴有大鼠胸腺移植物的淋巴细胞耗竭,因此可用于评估TCDD效应的重症联合免疫缺陷-大鼠小鼠数量有限。在重症联合免疫缺陷-大鼠小鼠中获得的数据与正常大鼠和移植的人类胸腺中的数据一致。在气相色谱/质谱分析中,正常大鼠胸腺和移植的人类胸腺中的TCDD组织浓度相似。我们得出结论,人类胸腺是TCDD的作用靶点,并且人类胸腺和Wistar大鼠胸腺对TCDD的毒性作用表现出可比的敏感性。

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