Loss of steroidogenic factor 1 alters cellular topography in the mouse ventromedial nucleus of the hypothalamus

被引:60
作者
Davis, AM
Seney, ML
Stallings, NR
Zhao, LP
Parker, KL
Tobet, SA [1 ]
机构
[1] Colorado State Univ, Ft Collins, CO 80523 USA
[2] Farmingham State Coll, Framingham, MA 01701 USA
[3] Univ Texas, SW Med Ctr, Dallas, TX 75390 USA
来源
JOURNAL OF NEUROBIOLOGY | 2004年 / 60卷 / 04期
关键词
neuronal migration; SF-1; orphan nuclear receptor; eGFP; VMH;
D O I
10.1002/neu.20030
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
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-I KO mice were indistinguishable, cells that normally localize precisely within the VMH were scattered more diffusely in adjacent regions in SF-I 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 of the transcription factors islet-1 and nkx2.1 also were displaced in SF-I KO mice. Independent of gene expression, birthdate analyses further suggested that cells with earlier birthdates were affected more severely by the loss of SF-I 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. (C) 2004 Wiley Periodicals, Inc.
引用
收藏
页码:424 / 436
页数:13
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