Zhang Tiancheng, Ru Yan Fei, Wu Bin, Dong Haiyan, Chen Liang, Zheng Jufen, Li Jianhui, Wang Xin, Wang Zhikai, Wang Xuemei, Shen Xiaorong, Wu Jun, Qian Jun, Miao Maohua, Gu Yihua, Shi Huijuan
NHC Key Lab of Reproduction Regulation, Shanghai Institute for Biomedical and Pharmaceutical Technologies, Fudan University, Shanghai, China.
Key Laboratory of Growth Regulation and Translational Research of Zhejiang Province, School of Life Sciences, Westlake University, Hangzhou, 310024, Zhejiang, China.
Cell Biosci. 2021 Jul 30;11(1):150. doi: 10.1186/s13578-021-00665-7.
Lead (Pb) exposure is a risk factor for male infertility, but the epigenetic changes in sperm DNAattributable to lead exposure is poorly defined.
In this study, we investigated whether low Pb exposure (< 10 µg/dL) affects the sperm quality. Blood, urine, and semen samples of 297 men of childbearing age were analyzed for all relevant parameters. Based on the blood Pb level (BLL), participants were allocated to RL (0-2.5 µg/dL), RM (2.5-5 µg/dL), and RH (5-10 µg/dL) groups. The 5-methylcytosine and 5-hydroxymethylcytosine patterns in the sperm DNA were identified using methylated DNA immunoprecipitation and hydroxymethylated DNA immunoprecipitation sequencing.
The non-progressive motility (NP) was significantly increased and associated with global hypomethylation of sperm DNA in the RH group compared with the RL group, indicating that aberrant sperm methylation due to low Pb exposure is possibly associated with reduced sperm motility. The hypomethylated promoter regions were primarily enriched in the calcium (Ca) homeostasis pathway. Further, the interaction between Ca and Pb was associated with sperm rapid progressive motility and asthenospermia risk, although no significant methylation abnormality was observed in those with BLL < 5 µg/dL. When BLL was > 5 µg/dL or when predicting NP, no significant Pb-Ca interaction was observed.
Overall, our results indicate that aberrant DNA methylation of the Ca homeostasis pathway, induced by low Pb exposure, is the potential cause for reduced sperm velocity.
铅(Pb)暴露是男性不育的一个风险因素,但铅暴露导致的精子DNA表观遗传变化尚不清楚。
在本研究中,我们调查了低铅暴露(<10μg/dL)是否会影响精子质量。对297名育龄男性的血液、尿液和精液样本进行了所有相关参数分析。根据血铅水平(BLL),参与者被分为RL(0 - 2.5μg/dL)、RM(2.5 - 5μg/dL)和RH(5 - 10μg/dL)组。使用甲基化DNA免疫沉淀和羟甲基化DNA免疫沉淀测序来鉴定精子DNA中的5 - 甲基胞嘧啶和5 - 羟甲基胞嘧啶模式。
与RL组相比,RH组的非进行性运动(NP)显著增加,且与精子DNA的整体低甲基化相关,这表明低铅暴露导致的异常精子甲基化可能与精子活力降低有关。低甲基化启动子区域主要富集在钙(Ca)稳态途径中。此外,Ca和Pb之间的相互作用与精子快速进行性运动和弱精子症风险相关,尽管在BLL <5μg/dL的人群中未观察到明显的甲基化异常。当BLL>5μg/dL或预测NP时,未观察到显著的Pb - Ca相互作用。
总体而言,我们的结果表明,低铅暴露诱导的Ca稳态途径的异常DNA甲基化是精子速度降低的潜在原因。