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人类胎儿睾丸的发育:细胞分化标志物的形态学与表达

Development of the human fetal testis: Morphology and expression of cellular differentiation markers.

作者信息

Li Yi, Overland Maya, Derpinghaus Amber, Aksel Sena, Cao Mei, Ladwig Nicholas, Cunha Gerald R, Baskin Laurence S

机构信息

Department of Urology, University of California, San Francisco, 400 Parnassus Avenue, San Francisco, CA, 94143, USA.

Department of Pathology, University of California, San Francisco, 505 Parnassus Avenue, San Francisco, CA, 94143, USA.

出版信息

Differentiation. 2023 Jan-Feb;129:17-36. doi: 10.1016/j.diff.2022.03.002. Epub 2022 Mar 25.

Abstract

A comprehensive immunohistochemical ontogeny of the developing human fetal testis has remained incomplete in the literature to date. We collected human fetal testes from 8 to 21 weeks of fetal age, as well as postnatal human testes at minipuberty, pre-pubertal, and pubertal stages. Immunohistochemistry was performed with a comprehensive panel of antigens targeting gonadocytes, Sertoli cells, fetal Leydig cells, peritubular myoid cells, and other hormonal and developmental targets. Testicular cords, precursor structures to seminiferous tubules, developed from 8 to 14 weeks of fetal age, separating the testis into the interstitial and intracordal compartments. Fetal gonadocytes were localized within the testicular cords and evaluated for Testis-Specific Protein Y, Octamer-binding transcription factor 4, Sal-like protein 4, and placental alkaline phosphatase expression. Fetal Sertoli cells were also localized in the testicular cords and evaluated for SRY-box Transcription Factor 9, inhibin, and anti-Mullerian hormone expression. Fetal Leydig cells were present in the interstitium and stained for cytochrome p450c17 and calretinin, while interstitial peritubular myoid cells were examined using smooth muscle α-actin staining. Androgen receptor expression was localized close to the testicular medulla at 8 weeks and then around the testicular cords in the interstitium as they matured in structure. Postnatal staining showed that Testis-Specific Protein Y remained positive of male gonadocytes throughout adulthood. Anti-Mullerian hormone, SRY-box Transcription Factor 9, and Steroidogenic factor 1 are expressed by the postnatal Sertoli cells at all ages examined. Leydig cell markers cytochrome p450c17 and calretinin are expressed during mini-puberty and puberty, but not expressed during the pre-pubertal period. Smooth muscle α-actin and androgen receptor were not expressed during mini-puberty or pre-puberty, but again expressed during the pubertal period. The ontogenic map of the human fetal and postnatal testicular structure and expression patterns described here will serve as a reference for future investigations into normal and abnormal testicular development.

摘要

迄今为止,发育中的人类胎儿睾丸完整的免疫组织化学个体发生情况在文献中仍不完整。我们收集了胎龄8至21周的人类胎儿睾丸,以及小青春期、青春期前和青春期阶段的出生后人类睾丸。使用一组全面的抗原进行免疫组织化学检测,这些抗原靶向生殖母细胞、支持细胞、胎儿睾丸间质细胞、睾丸肌样细胞以及其他激素和发育靶点。睾丸索是生精小管的前体结构,在胎龄8至14周时发育形成,将睾丸分隔为间质和索内区室。胎儿生殖母细胞定位于睾丸索内,并评估其睾丸特异性蛋白Y、八聚体结合转录因子4、Sal样蛋白4和胎盘碱性磷酸酶的表达。胎儿支持细胞也定位于睾丸索内,并评估其SRY盒转录因子9、抑制素和抗苗勒管激素的表达。胎儿睾丸间质细胞存在于间质中,用细胞色素p450c17和钙视网膜蛋白染色,而间质睾丸肌样细胞则用平滑肌α-肌动蛋白染色进行检测。雄激素受体表达在8周时定位于靠近睾丸髓质处,然后随着其结构成熟,在间质中的睾丸索周围表达。出生后的染色显示,睾丸特异性蛋白Y在成年男性的生殖母细胞中始终呈阳性。在所检测的所有年龄段,出生后的支持细胞均表达抗苗勒管激素、SRY盒转录因子9和类固醇生成因子1。睾丸间质细胞标志物细胞色素p450c17和钙视网膜蛋白在小青春期和青春期表达,但在青春期前不表达。平滑肌α-肌动蛋白和雄激素受体在小青春期或青春期前不表达,但在青春期再次表达。这里描述的人类胎儿和出生后睾丸结构及表达模式的个体发生图谱将为未来正常和异常睾丸发育的研究提供参考。

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