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致畸原诱导的小鼠全前脑畸形的发生机制。

Genesis of teratogen-induced holoprosencephaly in mice.

机构信息

University of North Carolina at Chapel Hill, 27599, USA.

出版信息

Am J Med Genet C Semin Med Genet. 2010 Feb 15;154C(1):29-42. doi: 10.1002/ajmg.c.30239.

Abstract

Evidence from mechanical, teratological, and genetic experimentation demonstrates that holoprosencephaly (HPE) typically results from insult prior to the time that neural tube closure is completed and occurs as a consequence of direct or indirect insult to the rostral prechordal cells that induce the forebrain or insult to the median forebrain tissue, itself. Here, we provide an overview of normal embryonic morphogenesis during the critical window for HPE induction, focusing on the morphology and positional relationship of the developing brain and subjacent prechordal plate and prechordal mesoderm cell populations. Subsequent morphogenesis of the HPE spectrum is then examined in selected teratogenesis mouse models. The temporal profile of Sonic Hedgehog expression in rostral embryonic cell populations and evidence for direct or indirect perturbation of the Hedgehog pathway by teratogenic agents in the genesis of HPE is highlighted. Emerging opportunities based on recent insights and new techniques to further characterize the mechanisms and pathogenesis of HPE are discussed.

摘要

来自机械、畸形学和遗传学实验的证据表明,前脑无裂畸形(HPE)通常是由于神经管闭合完成之前的损伤引起的,是由于对诱导前脑的颅前原条细胞或对中脑神经组织本身的直接或间接损伤而发生的。在这里,我们提供了 HPE 诱导关键窗口期正常胚胎形态发生的概述,重点介绍了发育中大脑和下方原条板和原条中胚层细胞群体的形态和位置关系。然后在选定的致畸剂小鼠模型中检查了 HPE 谱的后续形态发生。突出了 Sonic Hedgehog 在颅前胚胎细胞群中的表达时间图谱,以及致畸剂在 HPE 发生中对 Hedgehog 途径的直接或间接干扰的证据。讨论了基于最近的见解和新技术进一步表征 HPE 机制和发病机制的新机会。

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