胎儿亮德氏细胞:我们知道什么,我们不知道什么。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Keer Jiang, Joan S. Jorgensen
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引用次数: 0

摘要

在男性胎儿发育过程中,睾酮对男性生殖系统的分化和成熟起着至关重要的作用。胎儿睾酮分泌不足会导致性别分化的变化,从而可能导致不育,甚至增加日后的肿瘤发病率。胎儿睾丸中的胎儿莱德细胞是哺乳动物体内雄激素的主要来源。虽然胎儿和成人莱德细胞的功能相似,但它们是两种不同的细胞类型,因此,成人莱德细胞的知识不能直接用于了解胎儿莱德细胞。本综述总结了我们目前对胎儿莱德细胞的了解,包括细胞生物学、发育生物学以及啮齿动物和人类的雄激素分泌调控。胎儿Leydig细胞存在于睾丸索之间基底膜封闭的细胞簇中。它们起源于肾间质间充质和髓质上皮,在接收到来自Sertoli细胞的Desert Hedgehog信号或来自内皮细胞的NOTCH信号后开始分化。成熟的胎儿 Leydig 细胞可产生雄激素。人类胎儿 Leydig 细胞的类固醇生成依赖于 LHCGR(黄体生成素慢性促性腺激素受体),而啮齿类动物则不依赖,尽管其他 Gαs 蛋白偶联受体可能参与了啮齿类动物类固醇生成的调节。胎儿的类固醇生成在完成性别分化后停止,一些胎儿的莱迪格细胞发生再分化,成为成年睾丸细胞类型的干细胞。我们承认存在重大差距:(1) 为什么成人和胎儿的 Leydig 细胞不同?(2)什么是真正的祖细胞和胎儿 Leydig 细胞标记?(3)哪些信号通路和转录因子调控胎儿 Leydig 细胞的类固醇生成?找到这些问题的答案至关重要,只有这样,我们才能了解胎儿雷德氏细胞的脆弱靶点和雄激素生成机制,一旦这些机制被破坏,就会导致从细微到完全性别逆转的性别分化变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Fetal Leydig cells: What we know and what we don't

Fetal Leydig cells: What we know and what we don't

During male fetal development, testosterone plays an essential role in the differentiation and maturation of the male reproductive system. Deficient fetal testosterone production can result in variations of sex differentiation that may cause infertility and even increased tumor incidence later in life. Fetal Leydig cells in the fetal testis are the major androgen source in mammals. Although fetal and adult Leydig cells are similar in their functions, they are two distinct cell types, and therefore, the knowledge of adult Leydig cells cannot be directly applied to understanding fetal Leydig cells. This review summarizes our current knowledge of fetal Leydig cells regarding their cell biology, developmental biology, and androgen production regulation in rodents and human. Fetal Leydig cells are present in basement membrane-enclosed clusters in between testis cords. They originate from the mesonephros mesenchyme and the coelomic epithelium and start to differentiate upon receiving a Desert Hedgehog signal from Sertoli cells or being released from a NOTCH signal from endothelial cells. Mature fetal Leydig cells produce androgens. Human fetal Leydig cell steroidogenesis is LHCGR (Luteinizing Hormone Chronic Gonadotropin Receptor) dependent, while rodents are not, although other Gαs-protein coupled receptors might be involved in rodent steroidogenesis regulation. Fetal steroidogenesis ceases after sex differentiation is completed, and some fetal Leydig cells dedifferentiate to serve as stem cells for adult testicular cell types. Significant gaps are acknowledged: (1) Why are adult and fetal Leydig cells different? (2) What are bona fide progenitor and fetal Leydig cell markers? (3) Which signaling pathways and transcription factors regulate fetal Leydig cell steroidogenesis? It is critical to discover answers to these questions so that we can understand vulnerable targets in fetal Leydig cells and the mechanisms for androgen production that when disrupted, leads to variations in sex differentiation that range from subtle to complete sex reversal.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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