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缺乏L1-L1同源性黏附的小鼠的大脑发育

Brain development in mice lacking L1-L1 homophilic adhesion.

作者信息

Itoh Kyoko, Cheng Ling, Kamei Yoshimasa, Fushiki Shinji, Kamiguchi Hiroyuki, Gutwein Paul, Stoeck Alexander, Arnold Bernd, Altevogt Peter, Lemmon Vance

机构信息

Department of Neuroscience, Case Western Reserve University, Cleveland, OH 44106, USA.

出版信息

J Cell Biol. 2004 Apr;165(1):145-54. doi: 10.1083/jcb.200312107. Epub 2004 Apr 5.

Abstract

A new mouse line has been produced in which the sixth Ig domain of the L1 cell adhesion molecule has been deleted. Despite the rather large deletion, L1 expression is preserved at normal levels. In vitro experiments showed that L1-L1 homophilic binding was lost, along with L1-alpha5beta1 integrin binding. However, L1-neurocan and L1-neuropilin binding were preserved and sema3a responses were intact. Surprisingly, many of the axon guidance defects present in the L1 knockout mice, such as abnormal corticospinal tract and corpus callosum, were not observed. Nonetheless, when backcrossed on the C57BL/6 strain, a severe hydrocephalus was observed and after several generations, became an embryonic lethal. These results imply that L1 binding to L1, TAG-1, or F3, and L1-alpha5beta1 integrin binding are not essential for normal development of a variety of axon pathways, and suggest that L1-L1 homophilic binding is important in the production of X-linked hydrocephalus.

摘要

已经培育出一种新的小鼠品系,其中L1细胞粘附分子的第六个免疫球蛋白结构域已被删除。尽管有相当大的缺失,但L1表达仍保持在正常水平。体外实验表明,L1-L1同源结合以及L1-α5β1整合素结合丧失。然而,L1-神经粘蛋白和L1-神经纤毛蛋白结合得以保留,并且对sema3a的反应完整。令人惊讶的是,未观察到L1基因敲除小鼠中存在的许多轴突导向缺陷,如皮质脊髓束和胼胝体异常。尽管如此,当回交到C57BL/6品系时,观察到严重的脑积水,经过几代后,成为胚胎致死性疾病。这些结果表明,L1与L1、TAG-1或F3的结合以及L1-α5β1整合素结合对于多种轴突通路的正常发育并非必不可少,并表明L1-L1同源结合在X连锁脑积水的发生中很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/746b/2172083/e0dab5c9b6b8/200312107f1.jpg

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