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人类产前卵子发生过程中生殖细胞的凋亡。

Apoptosis of germ cells during human prenatal oogenesis.

作者信息

De Pol A, Vaccina F, Forabosco A, Cavazzuti E, Marzona L

机构信息

Dipartimento di Scienze Morfologiche e Medico Legali, Università di Modena, Italy.

出版信息

Hum Reprod. 1997 Oct;12(10):2235-41. doi: 10.1093/humrep/12.10.2235.

DOI:10.1093/humrep/12.10.2235
PMID:9402287
Abstract

During human oogenesis two contrasting processes can be observed: germ cell proliferation and differentiation, and contemporaneous germ cell death. It is well known that apoptosis is a type of physiological cell death that occurs in proliferating and differentiating tissues. The aim of this study is to demonstrate, through ultrastructural and in-situ 3' end labelling observations in intact sections of human fetal ovaries, that germ cell loss during fetal life is due to a phenomenon of apoptosis. We evaluated the presence of programmed cell death in female germ cells in fetal ovaries at 18-20 weeks of postconceptional age. The alterations that occur during apoptosis were detected by the electron microscope and include cytoplasmic condensation, organelle relocalization and compaction, chromatin condensation, and finally, production of membrane-enclosed particles containing intracellular material, known as apoptotic bodies, that are phagocytosed. The fragmentation of DNA, characteristic of apoptotic cells, was detected by the use of the in-situ 3' end labelling procedure on histological sections of ovaries where only some nuclei of germ cells were positively stained. The parallel use of these two methods on human ovaries of 18-20 weeks postconceptional age has allowed us to show that the numerical decrease of human female germ cells during the fetal period is due to an apoptotic phenomenon.

摘要

在人类卵子发生过程中,可以观察到两个截然不同的过程:生殖细胞的增殖与分化,以及同时发生的生殖细胞死亡。众所周知,细胞凋亡是一种发生在增殖和分化组织中的生理性细胞死亡。本研究的目的是通过对人类胎儿卵巢完整切片进行超微结构和原位3'末端标记观察,证明胎儿期生殖细胞的丢失是由于细胞凋亡现象所致。我们评估了孕龄18 - 20周胎儿卵巢中雌性生殖细胞程序性细胞死亡的情况。通过电子显微镜检测到细胞凋亡过程中发生的变化,包括细胞质浓缩、细胞器重新定位和聚集、染色质浓缩,最后产生含有细胞内物质的膜包裹颗粒,即凋亡小体,这些凋亡小体被吞噬。通过对卵巢组织切片使用原位3'末端标记程序检测到凋亡细胞特有的DNA片段化,在这些切片中只有一些生殖细胞核呈阳性染色。在孕龄18 - 20周的人类卵巢上同时使用这两种方法,使我们能够表明胎儿期人类雌性生殖细胞数量的减少是由于凋亡现象。

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