Characterization of urethra closure in female neonatal mice at histological and molecular levels.

IF 3.7 3区 生物学 Q1 DEVELOPMENTAL BIOLOGY
Reproduction Pub Date : 2024-09-26 Print Date: 2024-11-01 DOI:10.1530/REP-24-0239
Abigail S Kitakule, Ciro M Amato, Humphrey Hung-Chang Yao
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引用次数: 0

Abstract

In brief: Female hypospadias is a little-known and poorly studied birth defect. This research establishes an anatomical and molecular foundation for future research to investigate the origins of this defect.

Abstract: Hypospadias is a congenital anomaly of the external genitalia where the urethra does not properly close. In humans, hypospadias is mostly reported in male newborns, whereas in females hypospadias is rare, although it is generally considered to be under-reported. Improper urethra closure in the female genitalia can cause recurrent genitourinary tract infections and infertility. In mice, female hypospadias was induced by exposure to exogenous estrogenic compounds. Aside from the link between estrogen exposure and female hypospadias, the process of female urethra closure is largely unstudied, with the precise timing of urethra closure and associated molecular mechanisms remaining poorly understood. To address this gap, we determined when urethra closure occurs and identified gene expression patterns during the process of urethra closure in female neonatal mice from postnatal day (PND) 5 to 10. Using whole mount imaging and histology, we discovered that the initiation of urethra closure begins at PND7, and urethra closure is fully completed by PND10. To identify the genes associated with urethra closure, we conducted bulk RNA sequencing on female external genitalia prior to and after urethra closure. Gene ontology analyses revealed an increase in steroidogenic gene expression (Star, Hsd3b6, and Cyp17a1) during urethra closure, suggesting that the female genitalia locally produce steroids which could facilitate steroid signaling within the genitalia. With this study, we establish an anatomical timeline of female urethra closure and hypothesize a paracrine steroid signaling mechanism of urethra closure. These observations provide entry points to aid in further understanding external genital abnormalities, like hypospadias, in females.

从组织学和分子水平描述雌性新生小鼠尿道闭合的特征。
尿道下裂是一种先天性外生殖器畸形,尿道无法正常闭合。在人类中,尿道下裂多见于男性新生儿,而女性尿道下裂则很少见,但一般认为女性尿道下裂的报告率较低。女性生殖器尿道口闭合不全可导致反复泌尿生殖道感染和不孕。在小鼠中,外源性雌激素化合物会诱发雌性尿道下裂。除了雌激素暴露与雌性尿道下裂之间的联系外,雌性尿道闭合的过程在很大程度上还未得到研究,尿道闭合的精确时间和相关分子机制仍鲜为人知。为了填补这一空白,我们确定了尿道闭合发生的时间,并鉴定了出生后第 5 天至第 10 天雌性新生小鼠尿道闭合过程中的基因表达模式。通过整装成像和组织学研究,我们发现尿道闭合始于出生后第7天,到出生后第10天尿道完全闭合。为了确定与尿道闭合相关的基因,我们在尿道闭合之前和之后对雌性外生殖器进行了大量 RNA 测序。基因本体分析表明,在尿道闭合过程中,类固醇生成基因(Star、Hsd3b6和Cyp17a1)的表达增加,这表明雌性外生殖器局部会产生类固醇,从而促进生殖器内类固醇信号的传递。通过这项研究,我们确定了雌性尿道闭合的解剖时间表,并假设尿道闭合的旁分泌类固醇信号机制。这些观察结果为进一步了解女性尿道下裂等外生殖器异常现象提供了切入点。
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
Reproduction
Reproduction 生物-发育生物学
CiteScore
7.40
自引率
2.60%
发文量
199
审稿时长
4-8 weeks
期刊介绍: Reproduction is the official journal of the Society of Reproduction and Fertility (SRF). It was formed in 2001 when the Society merged its two journals, the Journal of Reproduction and Fertility and Reviews of Reproduction. Reproduction publishes original research articles and topical reviews on the subject of reproductive and developmental biology, and reproductive medicine. The journal will consider publication of high-quality meta-analyses; these should be submitted to the research papers category. The journal considers studies in humans and all animal species, and will publish clinical studies if they advance our understanding of the underlying causes and/or mechanisms of disease. Scientific excellence and broad interest to our readership are the most important criteria during the peer review process. The journal publishes articles that make a clear advance in the field, whether of mechanistic, descriptive or technical focus. Articles that substantiate new or controversial reports are welcomed if they are noteworthy and advance the field. Topics include, but are not limited to, reproductive immunology, reproductive toxicology, stem cells, environmental effects on reproductive potential and health (eg obesity), extracellular vesicles, fertility preservation and epigenetic effects on reproductive and developmental processes.
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