4.7 Article

Effects of low lead exposure on sperm quality and sperm DNA methylation in adult men

期刊

CELL AND BIOSCIENCE
卷 11, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s13578-021-00665-7

关键词

Low lead; Sperm motility; DNA methylation; Calcium and lead interaction; Calcium homeostasis regulation pathway

资金

  1. National Key R&D Program of China [2018YFC1005001]
  2. Foundation of Science and Technology Commission of Shanghai Municipality [17JC1420103]
  3. Shanghai Municipal Science and Technology Major Project [2017SHZDZX01]
  4. Youth Program of National Natural Science Foundation of China [31801252]
  5. Youth Program of Shanghai Municipal Health Commission [20204Y0276]
  6. Shanghai Municipal Health Commission Scientific Research Project [201640369]

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The study found that low lead exposure may lead to global hypomethylation of sperm DNA, reducing sperm motility and potentially contributing to decreased sperm velocity. Aberrant DNA methylation of the Ca homeostasis pathway induced by low lead exposure may be the underlying cause for reduced sperm velocity.
Instruction Lead (Pb) exposure is a risk factor for male infertility, but the epigenetic changes in sperm DNAattributable to lead exposure is poorly defined. Methods In this study, we investigated whether low Pb exposure (< 10 mu g/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 mu g/dL), RM (2.5-5 mu g/dL), and RH (5-10 mu g/dL) groups. The 5-methylcytosine and 5-hydroxymethylcytosine patterns in the sperm DNA were identified using methylated DNA immunoprecipitation and hydroxymethylated DNA immunoprecipitation sequencing. Results 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 mu g/dL. When BLL was > 5 mu g/dL or when predicting NP, no significant Pb-Ca interaction was observed. Discussion 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.

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