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首页> 外文期刊>Journal of neurobiology >Loss of steroidogenic factor 1 alters cellular topography in the mouse ventromedial nucleus of the hypothalamus.
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Loss of steroidogenic factor 1 alters cellular topography in the mouse ventromedial nucleus of the hypothalamus.

机译:类固醇生成因子1的丢失会改变小鼠下丘脑腹膜外核的细胞形貌。

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摘要

Knockout (KO) mice lacking the orphan nuclear receptor steroidogenic factor 1 (SF-1) exhibit marked structural abnormalities of the ventromedial nucleus of the hypothalamus (VMH). In this study, we sought to determine the molecular mechanisms underlying the VMH abnormalities. To trace SF-1-expressing neurons, we used a SF-1/enhanced green fluorescent protein (eGFP) transgene. Although the total numbers of eGFP-positive cells in wild-type (WT) and SF-1 KO mice were indistinguishable, cells that normally localize precisely within the VMH were scattered more diffusely in adjacent regions in SF-1 KO mice. This abnormal distribution is likely due to the loss of SF-1 expression in VMH neurons rather than secondary effects of deficient steroidogenesis, as redistribution also was seen in mice with a CNS-specific KO of SF-1. Thus, the absence of SF-1 alters the distribution of cells that normally form the VMH within the mediobasal hypothalamus. Consistent with this model, the hypothalamic expression patterns ofthe transcription factors islet-1 and nkx2.1 also were displaced in SF-1 KO mice. Independent of gene expression, birthdate analyses further suggested that cells with earlier birthdates were affected more severely by the loss of SF-1 than were later born cells. We conclude that the absence of SF-1 causes major changes in cellular arrangement within and around the developing VMH that result from altered cell migration. Copyright 2004 Wiley Periodicals, Inc. J Neurobiol 60: 424-436, 2004
机译:缺少孤儿核受体类固醇生成因子1(SF-1)的基因敲除(KO)小鼠表现出下丘脑(VMH)腹侧核的明显结构异常。在这项研究中,我们试图确定VMH异常的分子机制。为了追踪表达SF-1的神经元,我们使用了SF-1 /增强型绿色荧光蛋白(eGFP)转基因。尽管野生型(WT)和SF-1 KO小鼠中eGFP阳性细胞的总数是无法区分的,但通常精确定位在VMH内的细胞在SF-1 KO小鼠的相邻区域中散布得更分散。这种异常分布很可能是由于VMH神经元中SF-1表达的丧失,而不是缺乏类固醇生成的继发作用,因为在具有CNS特异性KO-1的小鼠中也发现了重新分布。因此,SF-1的缺乏改变了在中下丘脑下正常形成VMH的细胞的分布。与该模型一致,在SF-1 KO小鼠中,转录因子胰岛-1和nkx2.1的下丘脑表达模式也被置换。与基因表达无关,出生日期分析进一步表明,出生日期较早的细胞受SF-1损失的影响比后期出生的细胞更为严重。我们得出的结论是,SF-1的缺失会导致正在发展的VMH内和周围的细胞排列发生重大变化,这是由于细胞迁移的改变引起的。版权所有2004 Wiley Periodicals,Inc. J Neurobiol 60:424-436,2004

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