人类卵巢的发育:胎儿通过青春期卵巢形态、卵泡发生和细胞分化标志物的表达

IF 2.2 3区 生物学 Q4 CELL BIOLOGY
Maya R. Overland , Yi Li , Amber Derpinghaus , Sena Aksel , Mei Cao , Nicholas Ladwig , Gerald R. Cunha , Marta Himelreich-Perić , Laurence S. Baskin
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引用次数: 3

摘要

正常人类胎儿和出生后早期卵巢发育的定义对于准确诊断临床标本中是否存在功能性卵巢组织至关重要。通过收集从妊娠8周到出生后16年的人类卵巢标本的广泛的组织学和免疫组织化学发育个体发生,我们对胎儿早期至青春期后人类卵巢的正常蛋白表达模式进行了全面的免疫组织化学定位,并详细介绍了卵泡发育早期的特异性表达定义。正常胎儿和产后卵巢组织的定义是存在卵泡结构和特征性免疫组织化学染色模式,包括表达叉头盒蛋白L2(FOXL2)的颗粒细胞。然而,目前标准的免疫组织化学标记物阵列对卵巢基质组织的定义很差,需要更多的工作来识别新的标记物,以提高我们在性分化障碍患者性腺标本中准确识别卵巢基质成分的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of the human ovary: Fetal through pubertal ovarian morphology, folliculogenesis and expression of cellular differentiation markers

A definition of normal human fetal and early postnatal ovarian development is critical to the ability to accurately diagnose the presence or absence of functional ovarian tissue in clinical specimens. Through assembling an extensive histologic and immunohistochemical developmental ontogeny of human ovarian specimens from 8 weeks of gestation through 16 years of postnatal, we present a comprehensive immunohistochemical mapping of normal protein expression patterns in the early fetal through post-pubertal human ovary and detail a specific expression-based definition of the early stages of follicular development. Normal fetal and postnatal ovarian tissue is defined by the presence of follicular structures and characteristic immunohistochemical staining patterns, including granulosa cells expressing Forkhead Box Protein L2 (FOXL2). However, the current standard array of immunohistochemical markers poorly defines ovarian stromal tissue, and additional work is needed to identify new markers to advance our ability to accurately identify ovarian stromal components in gonadal specimens from patients with disorders of sexual differentiation.

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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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