纳米级氧化石墨烯通过诱导氧化应激和细胞凋亡而使猪卵母细胞质量恶化。

IF 3.2 3区 医学 Q2 GENETICS & HEREDITY
Yang Gao, Fuziaton Baharudin, Yunhai Zhang, Kaixiang Tan, Yongteng Zhang, Mengchan Li, Zizheng Liang, Mengting Wu, Mianqun Zhang, Dandan Zhang
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引用次数: 0

摘要

目的:纳米氧化石墨烯(nGO)作为一种工程碳纳米材料,在生物医学领域的应用有了显著的增长。鉴于这些物质在人体组织或器官中积累的可能性,必须全面评估非政府组织的毒理学概况,特别是在女性生殖健康方面。方法:将猪生发囊(GV)卵母细胞在38.5℃下培养至特定发育阶段进行后续分析。用成熟培养基将nGO稀释至终浓度分别为10、50、100、200 μg/ml。应用免疫染色和荧光强度定量技术评估nGO暴露对卵母细胞减数分裂成熟关键过程的影响。结果:我们观察到暴露于nGO导致猪卵母细胞在体外培养过程中减数分裂能力受损。具体来说,nGO暴露导致α-微管蛋白乙酰化水平降低和着丝点微管失配,从而破坏纺锤体/染色体组织并阻碍减数分裂进程。此外,nGO暴露扰乱了肌动蛋白动力学,潜在地阻碍了卵母细胞减数分裂过程中的纺锤体迁移和皮质极化。此外,在nGO暴露后,观察到ovastacin的错误定位和过早的胞吐。值得注意的是,nGO暴露会导致线粒体功能障碍、DNA损伤和氧化应激,最终引发细胞凋亡,阻碍猪卵母细胞的成熟和受精后胚胎的发育。结论:我们的研究结果强调了nGO对哺乳动物卵母细胞质量的潜在有害影响,同时也为环境纳米颗粒释放对雌性生殖细胞发育的影响提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exposure to nanoscale graphene oxide deteriorates the quality of porcine oocytes via induction of oxidative stress and the apoptosis.

Purpose: Nano graphene oxide (nGO), as a type of engineered carbon nanomaterial, has witnessed significant growth in biomedical applications. Given the likelihood of accumulation of these materials in human tissues or organs, it becomes imperative to comprehensively assess the toxicological profile of nGO, particularly concerning female reproductive health.

Methods: Germinal vesicle (GV) porcine oocytes were cultured at 38.5 °C to the specific developmental stage for subsequent analysis. The nGO was diluted with the maturation medium to the final concentrations of 10, 50, 100 and 200 μg/ml, respectively. Immunostaining and fluorescence intensity quantification were applied to assess the effects of nGO exposure on the key processes during the oocyte meiotic maturation.

Results: We observed that exposure to nGO led to compromised meiotic competency in porcine oocytes during in vitro culture. Specifically, nGO exposure resulted in reduced acetylation levels of α-tubulin and misattachment of kinetochore-microtubules, thereby disrupting spindle/chromosome organization and impeding meiotic progression. Furthermore, nGO exposure perturbed actin dynamics, potentially hindering spindle migration and cortical polarization during oocyte meiosis. Additionally, mislocalization and premature exocytosis of ovastacin were observed following nGO exposure. Notably, nGO exposure induced mitochondrial dysfunction, DNA damage, and oxidative stress, ultimately triggering apoptosis and impeding the maturation of porcine oocytes and the development of post-fertilized embryos.

Conclusion: Our findings underscore the potential deleterious effects of nGO on mammalian oocyte quality, while also contributing valuable insights into the impact of environmental nanoparticle release on female germ cell development.

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来源期刊
CiteScore
5.70
自引率
9.70%
发文量
286
审稿时长
1 months
期刊介绍: The Journal of Assisted Reproduction and Genetics publishes cellular, molecular, genetic, and epigenetic discoveries advancing our understanding of the biology and underlying mechanisms from gametogenesis to offspring health. Special emphasis is placed on the practice and evolution of assisted reproduction technologies (ARTs) with reference to the diagnosis and management of diseases affecting fertility. Our goal is to educate our readership in the translation of basic and clinical discoveries made from human or relevant animal models to the safe and efficacious practice of human ARTs. The scientific rigor and ethical standards embraced by the JARG editorial team ensures a broad international base of expertise guiding the marriage of contemporary clinical research paradigms with basic science discovery. JARG publishes original papers, minireviews, case reports, and opinion pieces often combined into special topic issues that will educate clinicians and scientists with interests in the mechanisms of human development that bear on the treatment of infertility and emerging innovations in human ARTs. The guiding principles of male and female reproductive health impacting pre- and post-conceptional viability and developmental potential are emphasized within the purview of human reproductive health in current and future generations of our species. The journal is published in cooperation with the American Society for Reproductive Medicine, an organization of more than 8,000 physicians, researchers, nurses, technicians and other professionals dedicated to advancing knowledge and expertise in reproductive biology.
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