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通过在小鼠子宫外使用胎儿激光手术破坏嗅球原基诱导胼胝体发育不全

Induction of agenesis of the corpus callosum by the destruction of anlage of the olfactory bulb using fetal laser surgery exo utero in mice.

作者信息

Naruse I, Keino H

机构信息

Department of Morphology, Institute for Developmental Research, Aichi Prefectural Colony, Japan.

出版信息

Brain Res Dev Brain Res. 1993 Jan 15;71(1):69-74. doi: 10.1016/0165-3806(93)90106-k.

Abstract

It has long been discussed why some congenital anomalies were often involved with abnormalities in other organs, for example, brain anomalies accompanied by limb anomalies or cleft palate. The mechanism of combined abnormalities has been mysterious, and usually explained as pleiotropism. A combination between agenesis of the olfactory bulb and agenesis of the corpus callosum has been reported. In the present experiments, it has been suggested that non-attachment of the olfactory nerve to the rostro-ventral tip of the telencephalon blocked the induction of the olfactory bulbs from the telencephalon in genetic arhinencephalic mouse embryos. It was shown that the destruction of the olfactory bulb anlage using fetal laser surgery exo utero becomes a trigger of agenesis of the corpus callosum and irregular connection of the anterior commissure in later morphogenesis of the mouse brain. We believe that a fetal surgical experiment like this will make clear the morphogenetic mechanism of the combined abnormalities that have been previously explained as pleiotropism.

摘要

长期以来,人们一直在探讨为什么某些先天性异常常常与其他器官的异常同时出现,例如,脑异常伴有肢体异常或腭裂。联合异常的机制一直很神秘,通常被解释为基因多效性。曾有报道称嗅球发育不全与胼胝体发育不全同时出现。在本实验中,我们发现,在遗传性无脑小鼠胚胎中,嗅神经未附着于端脑的吻腹端会阻碍端脑对嗅球的诱导。结果表明,在子宫外使用胎儿激光手术破坏嗅球原基会成为小鼠脑后期形态发生中胼胝体发育不全和前连合连接不规则的触发因素。我们相信,这样的胎儿外科实验将阐明此前被解释为基因多效性的联合异常的形态发生机制。

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