Maternal Exposure to Ozone During Implantation Promotes a Feminized Transcriptomic Profile in the Male Adolescent Liver.

IF 3.3 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM Endocrinology Pub Date : 2025-02-05 DOI:10.1210/endocr/bqaf018
Janice A Dye, Erica J Stewart, Mette C Schladweiler, Helen H Nguyen, Rachel D Grindstaff, William T Padgett, Anna A Fisher, Colette N Miller
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Abstract

Maternal exposure to ozone during implantation results in reduced fetal weight gain in rats. Offspring from ozone-exposed dams demonstrate sexually dimorphic risks to high-fat diet feeding in adolescence. To better understand the adolescent hepatic metabolic landscape following fetal growth restriction, RNA sequencing was performed to characterize the effects of ozone-induced fetal growth restriction on male and female offspring. Pregnant Long-Evans rats were exposed to filtered air or 0.8 ppm ozone for 4 hours on both gestation days 5 and 6 (n = 6/group). At approximately postnatal day 48, liver tissue was obtained for RNA sequencing from offspring. Peri-implantation exposure to ozone in the dam had greater effects on hepatic gene expression in male offspring than in the females. Interestingly, heatmaps of these differentially expressed genes suggested that male offspring from ozone-exposed dams had a transcriptomic pattern like that of female offspring. Using a filtered set of highly female-predominant genes (n = 390), 57% were upregulated in the male offspring from ozone-exposed dams. Upregulated canonical pathways included sirtuin and orexin signaling, estrogen receptor signaling, and integration of energy metabolism. Relatively few genes altered in the male offspring from ozone-exposed dams were associated with endpoints of sexual maturity, signifying the likely source of the observed feminization was not attributed to sex hormones. This study provides initial evidence that growth restriction in utero may increase the risk of hepatic feminization in male offspring. Additional work is needed to further understand the relationship between developmental undernutrition and feminization in the male liver.

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母体在植入期间暴露于臭氧会促进男性青少年肝脏的雌性化转录组谱。
在大鼠植入期间,母体暴露于臭氧导致胎儿体重增加减少。暴露于臭氧的水坝的后代在青春期高脂肪饮食中表现出性别二态性的风险。为了更好地了解胎儿生长限制后的青少年肝脏代谢景观,研究人员进行了RNA测序,以表征臭氧诱导的胎儿生长限制对雄性和雌性后代的影响。怀孕的Long-Evans大鼠在妊娠第5天和第6天暴露于过滤空气或0.8 ppm臭氧中4小时(n = 6/组)。大约在出生后第48天,从后代获得肝组织用于RNA测序。胚胎着床期接触臭氧对雄性后代肝脏基因表达的影响大于雌性后代。有趣的是,这些deg的热图表明,暴露于臭氧的水坝的雄性后代具有与雌性后代相似的转录组模式。使用一组过滤后的高度雌性优势基因(n = 390),在臭氧暴露坝的雄性后代中,57%的基因上调。上调的典型途径包括sirtuin和orexin信号,雌激素受体信号和能量代谢的整合。暴露于臭氧的雄性后代中,与性成熟终点相关的基因改变相对较少,这表明观察到的雌性化可能不是由性激素引起的。本研究提供了子宫内生长受限可能增加雄性后代肝脏雌性化风险的初步证据。要进一步了解发育性营养不良与男性肝脏女性化之间的关系,还需要进一步的工作。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Endocrinology
Endocrinology 医学-内分泌学与代谢
CiteScore
8.10
自引率
4.20%
发文量
195
审稿时长
2-3 weeks
期刊介绍: The mission of Endocrinology is to be the authoritative source of emerging hormone science and to disseminate that new knowledge to scientists, clinicians, and the public in a way that will enable "hormone science to health." Endocrinology welcomes the submission of original research investigating endocrine systems and diseases at all levels of biological organization, incorporating molecular mechanistic studies, such as hormone-receptor interactions, in all areas of endocrinology, as well as cross-disciplinary and integrative studies. The editors of Endocrinology encourage the submission of research in emerging areas not traditionally recognized as endocrinology or metabolism in addition to the following traditionally recognized fields: Adrenal; Bone Health and Osteoporosis; Cardiovascular Endocrinology; Diabetes; Endocrine-Disrupting Chemicals; Endocrine Neoplasia and Cancer; Growth; Neuroendocrinology; Nuclear Receptors and Their Ligands; Obesity; Reproductive Endocrinology; Signaling Pathways; and Thyroid.
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