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母体暴露于邻苯二甲酸二丁酯(DBP)会抑制食欲素受体1(OX1R)的表达,通过AKT信号通路阻止支持细胞增殖。

Maternal exposure to Di-n-butyl phthalate (DBP) inhibit orexin receptor 1 (OX1R) expression to prevent Sertoli cells proliferation through the AKT signaling pathway.

作者信息

Xie Zhiwen, Jiang Juntao, Li Tiewen, Xu Xinyu, Wu Lei, Zhang Yongqing, Chen Min, Sun Yang

机构信息

Department of Urology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, NO. 100 Hai Ning Road, Shanghai 200080, China.

Department of Urology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, NO. 160 Pu Jian Road, Shanghai 200127, China.

出版信息

Toxicol Res (Camb). 2024 Sep 3;13(5):tfae140. doi: 10.1093/toxres/tfae140. eCollection 2024 Oct.

Abstract

BACKGROUND

Studies have demonstrated that Sertoli cells are the direct target of Dibutyl phthalate (DBP). However, the role of neurotransmitter receptors is not elucidated.

METHODS

Based on our previous studies, maternal Sprague-Dawley (SD) rats in Gestation Day (GD) 14-18 and TM4 cells exposure to 750 mg/kg/day and 100 μM DBP were regarded as treated groups. Firstly, qRT-PCR array was used to determine the different expression of neurotransmitter receptors. We examined the OX1R expression on Rats in Control and DBP groups by immunohistochemistry. Real-time PCR and Western Blot were used to detect the protein and mRNA expression levels of OX1R in vivo and in vitro. The potential downstream signaling pathways were explored by analyzing the GSE99690 cohort. In addition, we extracted Primary Sertoli Cells (PSCs) from the testis of control group. The apoptosis-related proteins, AKT signaling pathway-related proteins and mRNA expressions were detected by Western Blot and Real-time PCR in PSCs. The validity of PSCs was measured by CCK-8 assay and flow cytometric analysis was used to demonstrate the apoptotic rates of PSCs after DBP exposure.

RESULTS

The Orexin receptor 1 (OX1R) was screened out by qRT-PCR array. Our results showed that DBP could significantly suppress the OX1R expression of Sertoli cells in vivo and in vitro. Functional analysis showed the AKT signaling pathway was mediated by OX1R. The highly expressed apoptosis level and impaired cell activity were observed in PSCs, which can be reversed by Orexin A. Meanwhile, the p-AKT signaling pathway were hindered after DBP exposure while rescued in DBP + Orexin-A group.

CONCLUSIONS

DBP can induce Sertoli cell apoptosis through its toxicological effect by suppressing OX1R and p-AKT expression, which provide a novel insight on the role of neurotransmitter receptors.

摘要

背景

研究表明,支持细胞是邻苯二甲酸二丁酯(DBP)的直接作用靶点。然而,神经递质受体的作用尚未阐明。

方法

基于我们之前的研究,将妊娠第14 - 18天的母性斯普拉格-道利(SD)大鼠以及TM4细胞暴露于750毫克/千克/天和100微摩尔的DBP中作为处理组。首先,使用qRT-PCR芯片来确定神经递质受体的差异表达。我们通过免疫组织化学检测对照和DBP组大鼠的OX1R表达。实时PCR和蛋白质免疫印迹法用于检测体内外OX1R的蛋白质和mRNA表达水平。通过分析GSE99690队列探索潜在的下游信号通路。此外,我们从对照组睾丸中提取原代支持细胞(PSCs)。通过蛋白质免疫印迹法和实时PCR检测PSCs中凋亡相关蛋白、AKT信号通路相关蛋白和mRNA表达。通过CCK-8法测定PSCs的活性,并使用流式细胞术分析来证明DBP暴露后PSCs的凋亡率。

结果

通过qRT-PCR芯片筛选出食欲素受体1(OX1R)。我们的结果表明,DBP可在体内外显著抑制支持细胞的OX1R表达。功能分析表明,AKT信号通路由OX1R介导。在PSCs中观察到高表达的凋亡水平和受损的细胞活性,而食欲素A可使其逆转。同时,DBP暴露后p-AKT信号通路受阻,而在DBP + 食欲素A组中得到挽救。

结论

DBP可通过抑制OX1R和p-AKT表达,通过其毒理学效应诱导支持细胞凋亡,这为神经递质受体的作用提供了新的见解。

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