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

IF 2.2 3区 生物学 Q4 CELL BIOLOGY Differentiation Pub Date : 2023-01-01 DOI:10.1016/j.diff.2022.03.002
Yi Li , Maya Overland , Amber Derpinghaus , Sena Aksel , Mei Cao , Nicholas Ladwig , Gerald R. Cunha , Laurence S. Baskin
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引用次数: 4

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.

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人胎儿睾丸的发育:细胞分化标记物的形态和表达
到目前为止,关于发育中的人类胎儿睾丸的全面免疫组织化学个体发育的文献还不完整。我们收集了8至21周胎儿年龄的人类胎儿睾丸,以及青春期、青春期前和青春期出生后的人类睾丸。免疫组织化学是用一组全面的抗原进行的,靶向性腺细胞、支持细胞、胎儿Leydig细胞、管周类肌细胞和其他激素和发育靶点。睾丸索是曲精管的前体结构,在胎儿8至14周时发育,将睾丸分为间质和睾丸内隔室。胎儿性腺细胞定位在睾丸索内,并评估睾丸特异性蛋白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在睾丸索中,并评估SRY-box转录因子9、抑制素和抗苗勒管激素的表达。胎儿Leydig细胞存在于间质中,并对细胞色素p450c17和钙视网膜蛋白进行染色,而间质管周肌样细胞则使用平滑肌α-肌动蛋白染色进行检查。雄激素受体的表达在8周时定位于睾丸髓质附近,然后在结构成熟时定位于间质中的睾丸索周围。产后染色显示,雄性性腺细胞的睾丸特异性蛋白Y在整个成年期保持阳性。抗苗勒管激素、SRY-box转录因子9和类固醇生成因子1在所有检查年龄的出生后支持细胞中表达。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,但在青春期前期不表达。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。本文描述的人类胎儿和出生后睾丸结构和表达模式的个体发育图将作为未来研究正常和异常睾丸发育的参考。
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来源期刊
Differentiation
Differentiation 生物-发育生物学
CiteScore
4.10
自引率
3.40%
发文量
38
审稿时长
51 days
期刊介绍: Differentiation is a multidisciplinary journal dealing with topics relating to cell differentiation, development, cellular structure and function, and cancer. Differentiation of eukaryotes at the molecular level and the use of transgenic and targeted mutagenesis approaches to problems of differentiation are of particular interest to the journal. The journal will publish full-length articles containing original work in any of these areas. We will also publish reviews and commentaries on topics of current interest. The principal subject areas the journal covers are: • embryonic patterning and organogenesis • human development and congenital malformation • mechanisms of cell lineage commitment • tissue homeostasis and oncogenic transformation • establishment of cellular polarity • stem cell differentiation • cell reprogramming mechanisms • stability of the differentiated state • cell and tissue interactions in vivo and in vitro • signal transduction pathways in development and differentiation • carcinogenesis and cancer • mechanisms involved in cell growth and division especially relating to cancer • differentiation in regeneration and ageing • therapeutic applications of differentiation processes.
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