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甲氧滴滴涕代谢物 HPTE 改变 C57BL/6 小鼠胚胎胸腺细胞的活力和分化。

Methoxychlor metabolite HPTE alters viability and differentiation of embryonic thymocytes from C57BL/6 mice.

机构信息

a School of Community and Global Health , Claremont Graduate University , Claremont , CA , USA.

b Department of Biology , University of La Verne , La Verne , CA , USA.

出版信息

J Immunotoxicol. 2018 Dec;15(1):104-118. doi: 10.1080/1547691X.2018.1474978.

Abstract

Endocrine-disrupting chemicals (EDC) are widespread in the built and natural environments. Heightened public awareness of their potential danger has led to concern about whether EDC and their metabolites have significant negative biological effects. Studies have shown that EDC like DDT and other organochlorine pesticides, such as methoxychlor (MXC), have adverse effects on immune cells, but no studies have addressed the impact of HPTE, the primary metabolite of MXC. To elucidate the presence and significance of HPTE adverse effects, this study explored the impact of HPTE on a critical window and component of immune system development, embryonic T-cell development. Lesions at this phase of development can lead to lifelong immune dysfunction and increased incidence of immune disease, such as autoimmunity. Embry-onic thymocytes (GD 16-18) from C57BL/6 mice were subjected to an in vitro differentiation culture that mimicked early steps in thymocyte development in the presence of 0.005, 0.05, 0.5, 5, or 50 μM HPTE, or a model endocrine disruptor, DES. The results indicated that compared to the vehicle control, HPTE- and DES-induced death of thymocytes. Annexin-V staining and Caspase 8, markers of programed cell death, revealed that the loss of cells was due at least in part to induction of apoptosis. Moreover, HPTE-induced cell death not only resulted in selective loss of double positive thymocytes, but also loss of developing CD4 intermediate cells (post-double positive partially differentiated thymocyte population). Phenotypic analysis of thymocyte maturation (T-cell receptor, TCR) and TCR ligation (CD5) surface markers revealed that surviving embryonic thymocytes expressed low levels of both. Taken together these data demonstrate that immature embryonic thymocytes are sensitive to HPTE exposure and that HPTE exposure targets thymocyte populations undergoing critical differentiation steps. These findings suggest HPTE may play a pivotal role in MXC exposure-induced immune dysfunction.

摘要

内分泌干扰化学物质(EDC)广泛存在于建筑和自然环境中。公众对其潜在危险的认识不断提高,导致人们担忧 EDC 及其代谢物是否会产生重大的负面生物学影响。研究表明,DDT 等 EDC 和其他有机氯农药(如甲氧滴滴涕,MXC)对免疫细胞有不良影响,但尚无研究探讨 MXC 的主要代谢物 HPTE 的影响。为了阐明 HPTE 不良影响的存在和意义,本研究探讨了 HPTE 对免疫系统发育关键窗口和关键组成部分——胚胎 T 细胞发育的影响。该发育阶段的损伤可导致终生免疫功能障碍和免疫性疾病(如自身免疫)发病率增加。来自 C57BL/6 小鼠的胚胎胸腺细胞(GD 16-18)在 0.005、0.05、0.5、5 或 50μM HPTE 或模型内分泌干扰物 DES 存在的情况下进行体外分化培养,模拟胸腺细胞发育的早期步骤。结果表明,与载体对照组相比,HPTE 和 DES 诱导胸腺细胞死亡。Annexin-V 染色和 Caspase 8(程序性细胞死亡的标志物)表明细胞的丢失至少部分是由于诱导细胞凋亡所致。此外,HPTE 诱导的细胞死亡不仅导致双阳性胸腺细胞的选择性丢失,而且还导致发育中的 CD4 中间细胞(双阳性后部分分化的胸腺细胞群体)丢失。对胸腺细胞成熟(T 细胞受体,TCR)和 TCR 配体(CD5)表面标志物的表型分析显示,存活的胚胎胸腺细胞均低表达这两种标志物。总之,这些数据表明,未成熟的胚胎胸腺细胞对 HPTE 暴露敏感,HPTE 暴露针对的是正在经历关键分化步骤的胸腺细胞群体。这些发现表明,HPTE 可能在 MXC 暴露诱导的免疫功能障碍中发挥关键作用。

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