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父源镉暴露对卵巢颗粒细胞凋亡的多代遗传效应。

Multigenerational genetic effects of paternal cadmium exposure on ovarian granulosa cell apoptosis.

作者信息

Sun Yi, Zhang Wenchang, Li Yuchen, Zhu Jianlin, Liu Chenchen, Luo Lingfeng, Liu Jin, Zhang Chenyun

机构信息

Department of Preventive Medicine, Fujian Provincial Key Laboratory of Environmental Factors and Cancer, Key Laboratory of Environment and Health, School of Public Health, Fujian Medical University, Fuzhou 350122, Fujian Province, China; Key Laboratory of Environment and Female Reproductive Health, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.

Department of Preventive Medicine, Fujian Provincial Key Laboratory of Environmental Factors and Cancer, Key Laboratory of Environment and Health, School of Public Health, Fujian Medical University, Fuzhou 350122, Fujian Province, China.

出版信息

Ecotoxicol Environ Saf. 2023 Jun 12;262:115123. doi: 10.1016/j.ecoenv.2023.115123.

Abstract

To explore whether paternal cadmium (Cd) exposure causes ovarian granulosa cell (GC) apoptosis in offspring and the multigenerational genetic effects. From postnatal day 28 (PND28) until adulthood (PND56), SPF male Sprague-Dawley (SD) rats were gavaged daily with varying concentrations of CdCl (0, 0.5, 2, and 8 mg/kg). After treatment, the F1 generation was produced by mating with untreated female rats, and the F1 generation male rats were mated with untreated female rats to produce the F2 generation. Apoptotic bodies (electron microscopy) and significantly higher apoptotic rates (flow cytometry) were observed in both F1 and F2 ovarian GCs following paternal Cd exposure. Moreover, the mRNA (qRTPCR) or protein (Western blotting) levels of bax, bcl2, bcl-xl, caspase 3, caspase 8, and caspase 9 were changed to varying degrees. Apoptosis-related miRNAs (qRTPCR) and methylation modifications of apoptosis-related genes (bisulfite-sequencing PCR) in ovarian GCs were further detected. Compared with those of controls, the expression patterns of miRNAs in F1 and F2 offspring were different after paternal Cd exposure, while the average methylation level of apoptosis-related genes did not change significantly (except for individual loci). In summary, there are paternal genetic intergenerational and transgenerational effects on ovarian GC apoptosis induced by paternal Cd exposure. These genetic effects were related to the upregulation of BAX, BCL-XL, Cle-CASPASE 3, and Cle-CASPASE 9 in F1 and the upregulation of Cle-CASPASE 3 in F2 progeny. Important changes in apoptosis-related miRNAs were also observed.

摘要

为探究父源性镉(Cd)暴露是否会导致子代卵巢颗粒细胞(GC)凋亡以及多代遗传效应。从出生后第28天(PND28)至成年期(PND56),对特定病原体-free(SPF)级雄性斯普拉格-道利(SD)大鼠每日灌胃不同浓度的CdCl(0、0.5、2和8mg/kg)。处理后,F1代通过与未处理的雌性大鼠交配产生,F1代雄性大鼠再与未处理的雌性大鼠交配产生F2代。在父源性镉暴露后,F1和F2代卵巢颗粒细胞中均观察到凋亡小体(电子显微镜观察)以及显著更高的凋亡率(流式细胞术检测)。此外,bax、bcl2、bcl-xl、caspase 3、caspase 8和caspase 9的mRNA(qRTPCR)或蛋白(蛋白质印迹法)水平发生了不同程度的变化。进一步检测了卵巢颗粒细胞中凋亡相关的微小RNA(qRTPCR)以及凋亡相关基因的甲基化修饰(亚硫酸氢盐测序PCR)。与对照组相比,父源性镉暴露后F1和F2代子代中微小RNA的表达模式不同,而凋亡相关基因的平均甲基化水平未发生显著变化(个别位点除外)。综上所述,父源性镉暴露诱导的卵巢颗粒细胞凋亡存在父源性遗传的代际和跨代效应。这些遗传效应与F1代中BAX、BCL-XL、Cle-CASPASE 3和Cle-CASPASE 9的上调以及F2代子代中Cle-CASPASE 3的上调有关。同时也观察到了凋亡相关微小RNA的重要变化。

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