Steves Alyse N, Turry Adam, Gill Brittany, Clarkson-Townsend Danielle, Bradner Joshua M, Bachli Ian, Caudle W Michael, Miller Gary W, Chan Anthony W S, Easley Charles A
a Genetics and Molecular Biology Program , Laney Graduate School, Emory University , Atlanta , GA , USA.
b College of Public Health , University of Georgia , Athens , GA , USA.
Syst Biol Reprod Med. 2018 Aug;64(4):225-239. doi: 10.1080/19396368.2018.1481465. Epub 2018 Jun 18.
Per- and polyfluoroalkyl substances (PFASs) represent a highly ubiquitous group of synthetic chemicals used in products ranging from water and oil repellents and lubricants to firefighting foam. These substances can enter and accumulate in multiple tissue matrices in up to 100% of people assessed. Though animal models strongly identify these compounds as male reproductive toxicants, with exposed rodents experiencing declines in sperm count, alterations in hormones, and DNA damage in spermatids, among other adverse outcomes, human studies report conflicting conclusions as to the reproductive toxicity of these chemicals. Using an innovative, human stem-cell-based model of spermatogenesis, we assessed the effects of the PFASs perfluorooctanesulfonic acid (PFOS), perfluorooctanoic acid (PFOA), perfluorononanoic acid (PFNA), and a mixture of PFOS, PFOA, and PFNA for their impacts on human spermatogenesis in vitro under conditions relevant to the general and occupationally exposed populations. Here, we show that PFOS, PFOA, PFNA, and a mixture of PFOS, PFOA, and PFNA do not decrease in vitro germ cell viability, consistent with reports from human studies. These compounds do not affect mitochondrial membrane potential or increase reactive oxygen species generation, and they do not decrease cell viability of spermatogonia, primary spermatocytes, secondary spermatocytes, or spermatids in vitro under the conditions examined. However, exposure to PFOS, PFOA, and PFNA reduces expression of markers for spermatogonia and primary spermatocytes. While not having direct effects on germ cell viability, these effects suggest the potential for long-term impacts on male fertility through the exhaustion of the spermatogonial stem cell pool and abnormalities in primary spermatocytes.
CDC: Centers for Disease Control; DMSO: dimethyl sulfoxide; GHR: growth hormone receptor; hESCs: human embryonic stem cells; PFASs: per- and polyfluoroalkyl substances; PFCs: perfluorinated compounds; PFNA: perfluorononanoic acid; PFOS: perfluorooctanesulfonic acid; PFOA: perfluorooctanoic acid; PLZF: promyelocytic leukemia zinc finger; ROS: reactive oxygen species; HILI: RNA-mediated gene silencing 2; SSC: spermatogonial stem cell.
全氟和多氟烷基物质(PFASs)是一类极为普遍的合成化学品,用于从防水防油剂、润滑剂到消防泡沫等各类产品中。这些物质可进入并累积在多达100%接受评估的人的多种组织基质中。尽管动物模型有力地将这些化合物鉴定为雄性生殖毒物,暴露的啮齿动物出现精子数量减少、激素改变以及精子细胞DNA损伤等不良后果,但关于这些化学物质的生殖毒性,人体研究报告的结论相互矛盾。我们使用一种基于人类干细胞的创新精子发生模型,评估了全氟辛烷磺酸(PFOS)、全氟辛酸(PFOA)、全氟壬酸(PFNA)以及PFOS、PFOA和PFNA的混合物在与一般人群和职业暴露人群相关的条件下对体外人类精子发生的影响。在此,我们表明PFOS、PFOA、PFNA以及PFOS、PFOA和PFNA的混合物不会降低体外生殖细胞活力,这与人体研究报告一致。这些化合物不会影响线粒体膜电位或增加活性氧的产生,并且在所检测的条件下,它们不会降低精原细胞、初级精母细胞、次级精母细胞或精子细胞的细胞活力。然而,暴露于PFOS、PFOA和PFNA会降低精原细胞和初级精母细胞标志物的表达。虽然对生殖细胞活力没有直接影响,但这些影响表明可能会通过精原干细胞池的耗尽和初级精母细胞的异常对男性生育能力产生长期影响。
CDC:疾病控制中心;DMSO:二甲基亚砜;GHR:生长激素受体;hESCs:人类胚胎干细胞;PFASs:全氟和多氟烷基物质;PFCs:全氟化合物;PFNA:全氟壬酸;PFOS:全氟辛烷磺酸;PFOA:全氟辛酸;PLZF:早幼粒细胞白血病锌指蛋白;ROS:活性氧;HILI:RNA介导的基因沉默2;SSC:精原干细胞