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调控早期滋养层细胞分化——来自小鼠的启示。

Regulation of early trophoblast differentiation - lessons from the mouse.

机构信息

Laboratory for Developmental Genetics & Imprinting, The Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.

出版信息

Placenta. 2010 Nov;31(11):944-50. doi: 10.1016/j.placenta.2010.07.013. Epub 2010 Aug 24.

Abstract

The earliest stages of trophoblast differentiation are of tremendous importance to mediate implantation and to lay the anatomical foundations for normal placental development and function throughout gestation. Yet our molecular insights into these early developmental processes in humans have been limited by the inaccessibility of material and the unavailability of trophoblast cell lines that fully recapitulate the behaviour of early placental trophoblast. In this review we highlight recent advances that have come from the study of distinct stem cell types representative of the embryonic and extraembryonic lineages in the mouse, and from the study of mouse mutants. These models have revealed the presence of intricate transcriptional networks that are set up by signalling pathways, translating extracellular growth factor and cell positional information into distinct lineage-specific transcriptional programmes. The trophoblast specificity of these networks is ensured by epigenetic mechanisms including DNA methylation and histone modifications that complement each other to define trophoblast cell fate and differentiation. Despite the anatomical differences between mouse and human placentas, it seems that important aspects of early trophoblast specification are conserved between both species. Thus we may be able to build on our insights from the mouse to better understand early trophoblast differentiation in the human conceptus which is important for improving assisted reproductive technologies and may enable us in the future to derive human trophoblast stem cell lines. These advances will facilitate the investigation of genetic, epigenetic and environmental influences on early trophoblast differentiation in normal as well as in pathological conditions.

摘要

滋养层细胞分化的早期阶段对于介导着床以及为整个妊娠期正常胎盘发育和功能奠定解剖学基础至关重要。然而,由于人类无法获得相关材料,并且缺乏能够完全再现早期胎盘滋养层行为的滋养层细胞系,我们对这些早期发育过程的分子认识一直受到限制。在这篇综述中,我们重点介绍了一些最新的研究进展,这些进展来自于对具有代表性的胚胎和胚胎外谱系的不同干细胞类型的研究,以及对小鼠突变体的研究。这些模型揭示了存在复杂的转录网络,这些网络是由信号通路建立的,将细胞外生长因子和细胞位置信息转化为特定的谱系特异性转录程序。这些网络的滋养层特异性是通过表观遗传机制(包括 DNA 甲基化和组蛋白修饰)来保证的,这些机制相互补充,以确定滋养层细胞的命运和分化。尽管小鼠和人类胎盘在解剖结构上存在差异,但似乎在这两个物种之间,早期滋养层特化的重要方面是保守的。因此,我们可以借鉴从小鼠中获得的见解,更好地理解人类胚胎中的早期滋养层分化,这对于改善辅助生殖技术非常重要,并可能使我们在未来能够获得人类滋养层干细胞系。这些进展将有助于研究遗传、表观遗传和环境因素对正常和病理条件下早期滋养层分化的影响。

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