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本文引用的文献

1
The imbalance of Treg/Th17 cells induced by perinatal bisphenol A exposure is associated with activation of the PI3K/Akt/mTOR signaling pathway in male offspring mice.围生期双酚 A 暴露诱导的 Treg/Th17 细胞失衡与雄性子代小鼠 PI3K/Akt/mTOR 信号通路的激活有关。
Food Chem Toxicol. 2020 Mar;137:111177. doi: 10.1016/j.fct.2020.111177. Epub 2020 Feb 3.
2
Exposure to Bisphenol A and Bisphenol S and Incident Type 2 Diabetes: A Case-Cohort Study in the French Cohort D.E.S.I.R.双酚 A 和双酚 S 暴露与 2 型糖尿病发病风险:法国 DESIR 队列研究中的病例对照研究
Environ Health Perspect. 2019 Oct;127(10):107013. doi: 10.1289/EHP5159. Epub 2019 Oct 30.
3
Effect of developmental exposure to bisphenol A on steroid hormone and vitamin D3 metabolism.发育过程中双酚 A 的暴露对类固醇激素和维生素 D3 代谢的影响。
Chemosphere. 2019 Dec;237:124469. doi: 10.1016/j.chemosphere.2019.124469. Epub 2019 Aug 1.
4
Emerging role of vitamin D in autoimmune diseases: An update on evidence and therapeutic implications.维生素 D 在自身免疫性疾病中的新作用:证据和治疗意义的更新。
Autoimmun Rev. 2019 Sep;18(9):102350. doi: 10.1016/j.autrev.2019.102350. Epub 2019 Jul 16.
5
The adverse health effects of bisphenol A and related toxicity mechanisms.双酚 A 及其相关毒性机制的不良健康影响。
Environ Res. 2019 Sep;176:108575. doi: 10.1016/j.envres.2019.108575. Epub 2019 Jul 3.
6
The IL-17 Family of Cytokines in Health and Disease.白细胞介素-17 细胞因子家族在健康和疾病中的作用。
Immunity. 2019 Apr 16;50(4):892-906. doi: 10.1016/j.immuni.2019.03.021.
7
Immunological effects of vitamin D and their relations to autoimmunity.维生素 D 的免疫作用及其与自身免疫的关系。
J Autoimmun. 2019 Jun;100:7-16. doi: 10.1016/j.jaut.2019.03.002. Epub 2019 Mar 8.
8
Endocrine disruptors and the future of toxicology testing - lessons from CLARITY-BPA.内分泌干扰物与毒理学测试的未来——CLARITY-BPA 的启示。
Nat Rev Endocrinol. 2019 Jun;15(6):366-374. doi: 10.1038/s41574-019-0173-y.
9
1,25(OH) D inhibited Th17 cells differentiation via regulating the NF-κB activity and expression of IL-17.1,25(OH) D 通过调节 NF-κB 活性和 IL-17 的表达抑制 Th17 细胞分化。
Cell Prolif. 2018 Oct;51(5):e12461. doi: 10.1111/cpr.12461. Epub 2018 Apr 24.
10
Vitamin D3 inhibits the proliferation of T helper cells, downregulate CD4 T cell cytokines and upregulate inhibitory markers.维生素D3可抑制辅助性T细胞的增殖,下调CD4 T细胞细胞因子,并上调抑制性标志物。
Hum Immunol. 2018 Jun;79(6):439-445. doi: 10.1016/j.humimm.2018.03.001. Epub 2018 Mar 6.

母体维生素 D 补充可抑制双酚 A 诱导的成年子代 Th17 细胞增殖。

Maternal vitamin D supplementation inhibits bisphenol A-induced proliferation of Th17 cells in adult offspring.

机构信息

Department of Occupational Health and Environmental Health, School of Public Health, Anhui Medical University, Hefei, 230032, Anhui, PR China.

Department of Toxicology, School of Public Health, Anhui Medical University, Hefei, 230032, Anhui, PR China.

出版信息

Food Chem Toxicol. 2020 Oct;144:111604. doi: 10.1016/j.fct.2020.111604. Epub 2020 Jul 20.

DOI:10.1016/j.fct.2020.111604
PMID:32702508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11970977/
Abstract

Bisphenol A (BPA) exposure can increase the risk of immune-related diseases in later life. Vitamin D3 (Vit D3) has been shown to have multiple immunomodulatory actions and has been used to treat immune diseases. However, the potential beneficial effects of Vit D3 on BPA-induced adverse effects in the immune system have not explored. We hypothesize that VitD3 may ameliorate BPA-induced side effects in the immune system, even in offspring of VitD3-supplemented mothers. Here, we established our experimental model by exposing pregnant dams with 1000 nM BPA with or without VitD3 (0.25 μg/kg, 1 μg/kg and 4 μg/kg) treatment. We show that mother's exposure to BPA increases proliferation of the spleen T helper 17 (Th17) cells and serum protein level of IL-17 in the offspring; however, VitD3 supplementation in mothers dose-dependently ameliorated these BPA-induced side effects on the immune system in the offspring as evidenced by attenuated upregulation of Th17 proliferation, and RORγt, IL-17, IL-6, and IL-23 expressions in the offspring. Our data provide the first evidence that maternal VitD3 supplementation offers benefits to the offspring by attenuating BPA-induced side effects on the immune system through vitamin D receptor (VDR)-dependent regulation of transcription factors and cytokines, suggesting its translational potential.

摘要

双酚 A(BPA)暴露会增加晚年患免疫相关疾病的风险。维生素 D3(Vit D3)已被证明具有多种免疫调节作用,并已被用于治疗免疫疾病。然而,Vit D3 对 BPA 诱导的免疫系统不良影响的潜在有益作用尚未得到探索。我们假设 VitD3 可能会改善 BPA 诱导的免疫系统副作用,即使在 VitD3 补充母亲的后代中也是如此。在这里,我们通过用 1000 nM BPA 暴露怀孕的母鼠并伴有或不伴有 VitD3(0.25μg/kg、1μg/kg 和 4μg/kg)处理来建立我们的实验模型。我们发现母鼠暴露于 BPA 会增加脾脏 T 辅助 17(Th17)细胞的增殖和后代血清中白细胞介素 17(IL-17)的蛋白水平;然而,母鼠补充 VitD3 可剂量依赖性地改善这些 BPA 对后代免疫系统的副作用,这表现在 Th17 增殖、RORγt、IL-17、IL-6 和 IL-23 的表达下调。我们的数据首次提供了证据,即通过维生素 D 受体(VDR)依赖性转录因子和细胞因子调节,母体 VitD3 补充为后代提供了益处,减轻了 BPA 对免疫系统的副作用,这表明其具有转化潜力。