Single-Cell Metallomics of ovarian granulosa cells enables assessment of Low-Level heavy metal exposure associated with impaired human oocyte development

IF 10.2 1区 环境科学与生态学 Q1 ENVIRONMENTAL SCIENCES
Environment International Pub Date : 2026-10-01 Epub Date: 2026-10-10 DOI:10.1016/j.envint.2026.110559
Tong An, Guohuan Zhang, Nian Liu, Bin Liang, Ziyi Song, Lei Fu, Xueyan Bai, Shuo Han, Qun Lu, Ligang Hu
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Abstract

The oocyte microenvironment, comprising ovarian granulosa cells (GCs) and follicular fluid (FF), sustains oocyte development with nutrients and regulatory signals but may also transfer heavy metals to the oocyte. While high concentrations of heavy metals in FF and blood have been associated with impaired oocyte development, the effect of low-level exposure on the oocyte remains unclear, partly due to the analytical challenges in measuring low-level heavy metals in biological fluids. Here, we investigated the associations between low-level heavy metal exposure and oocyte development. Using a highly sensitive single-cell metallomic technique, we analyzed ovarian GCs collected from women undergoing in vitro fertilization and embryo transfer (IVF-ET) to serve as a biomarker of intracellular heavy metal burden in the peri-oocyte microenvironment. The associations between heavy metals in GCs and reproductive outcomes across multiple key reproductive stages were analyzed. Our results showed that the heavy metals content in GCs were generally below 0.5 fg/cell. Higher mean intensities and prevalence of several metals in GCs were significantly associated with reduced oocyte maturation rate, normal fertilization rate, and good-quality embryo rate (all adjusted P < 0.05). Elevated intracellular levels of lead and mercury were also associated with adverse reproductive outcomes and increased risk of early miscarriage. In contrast, higher heterogeneity of Hg within GCs was associated with reduced miscarriage risk (OR = 0.37 [0.04, 0.92], P = 0.034). Notably, these associations are significantly contributed by intercellular heterogeneity of metal accumulation within the GC population. Our study demonstrates the feasibility of applying single-cell metallomic technique to ovarian GCs to assess the reproductive risk associated with low-level intracellular heavy metal burden in ovarian follicles, and underscores the need for further reducing environmental heavy metal exposure to protect female reproductive health.
卵巢颗粒细胞的单细胞金属组学能够评估与人类卵母细胞发育受损相关的低水平重金属暴露。
卵母细胞微环境由卵巢颗粒细胞(GCs)和卵泡液(FF)组成,通过营养和调节信号维持卵母细胞的发育,但也可能将重金属转移到卵母细胞。虽然FF和血液中的高浓度重金属与卵母细胞发育受损有关,但低水平接触对卵母细胞的影响尚不清楚,部分原因是在测量生物体液中的低水平重金属时存在分析挑战。在这里,我们研究了低水平重金属暴露与卵母细胞发育之间的关系。利用高灵敏度的单细胞金属学技术,研究人员分析了体外受精和胚胎移植(IVF-ET)妇女卵巢GCs作为卵周微环境中细胞内重金属负荷的生物标志物。分析了GCs中重金属与多个关键生殖阶段的生殖结果之间的关系。结果表明,gc中重金属含量普遍低于0.5 fg/cell。GCs中较高的平均强度和几种金属的流行与卵母细胞成熟率降低、正常受精率和优质胚胎率显著相关
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来源期刊
Environment International
Environment International 环境科学-环境科学
CiteScore
21.90
自引率
3.40%
发文量
734
审稿时长
2.8 months
期刊介绍: Environmental Health publishes manuscripts focusing on critical aspects of environmental and occupational medicine, including studies in toxicology and epidemiology, to illuminate the human health implications of exposure to environmental hazards. The journal adopts an open-access model and practices open peer review. It caters to scientists and practitioners across all environmental science domains, directly or indirectly impacting human health and well-being. With a commitment to enhancing the prevention of environmentally-related health risks, Environmental Health serves as a public health journal for the community and scientists engaged in matters of public health significance concerning the environment.
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