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接触环境内分泌干扰物2,3,7,8-四氯二苯并对二恶英与人类生殖功能障碍:从小鼠模型中汲取的经验教训

Exposure to the environmental endocrine disruptor TCDD and human reproductive dysfunction: Translating lessons from murine models.

作者信息

Bruner-Tran Kaylon L, Gnecco Juan, Ding Tianbing, Glore Dana R, Pensabene Virginia, Osteen Kevin G

机构信息

Women's Reproductive Health Research Center, Department of Obstetrics & Gynecology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

Women's Reproductive Health Research Center, Department of Obstetrics & Gynecology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

出版信息

Reprod Toxicol. 2017 Mar;68:59-71. doi: 10.1016/j.reprotox.2016.07.007. Epub 2016 Jul 14.

Abstract

Humans and other animals are exposed to a wide array of man-made toxicants, many of which act as endocrine disruptors that exhibit differential effects across the lifespan. In humans, while the impact of adult exposure is known for some compounds, the potential consequences of developmental exposure to endocrine disrupting chemicals (EDCs) is more difficult to ascertain. Animal studies have revealed that exposure to EDCs prior to puberty can lead to adult reproductive disease and dysfunction. Specifically, in adult female mice with an early life exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD), we demonstrated a transgenerational occurrence of several reproductive diseases that have been linked to endometriosis in women. Herein, we review the evidence for TCDD-associated development of adult reproductive disease as well as known epigenetic alterations associated with TCDD and/or endometriosis. We will also introduce new "Organ-on-Chip" models which, combined with our established murine model, are expected to further enhance our ability to examine alterations in gene-environment interactions that lead to heritable disease.

摘要

人类和其他动物接触到各种各样的人造有毒物质,其中许多物质作为内分泌干扰物,在整个生命周期中表现出不同的影响。在人类中,虽然某些化合物对成年人接触的影响是已知的,但发育过程中接触内分泌干扰化学物质(EDCs)的潜在后果更难确定。动物研究表明,青春期前接触EDCs会导致成年期生殖疾病和功能障碍。具体而言,在成年雌性小鼠中,若其在生命早期接触2,3,7,8-四氯二苯并对二恶英(TCDD),我们发现了几种与女性子宫内膜异位症相关的生殖疾病会跨代发生。在此,我们回顾了TCDD与成年生殖疾病相关发展的证据,以及与TCDD和/或子宫内膜异位症相关的已知表观遗传改变。我们还将介绍新的“芯片器官”模型,该模型与我们已建立的小鼠模型相结合,有望进一步提高我们检查导致遗传性疾病的基因-环境相互作用改变的能力。

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