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通过谱系追踪揭示肾上腺皮质胎儿区与成人区之间的发育联系。

Developmental links between the fetal and adult zones of the adrenal cortex revealed by lineage tracing.

作者信息

Zubair Mohamad, Parker Keith L, Morohashi Ken-ichirou

机构信息

Division of Sex Differentiation, National Institute for Basic Biology, National Institutes of Natural Sciences,Okazaki, Japan.

出版信息

Mol Cell Biol. 2008 Dec;28(23):7030-40. doi: 10.1128/MCB.00900-08. Epub 2008 Sep 22.

Abstract

The nuclear receptor Ad4BP/SF-1 is essential for development of the adrenal cortex and the gonads, which derive from a common adrenogonadal primordium. The adrenal cortex subsequently forms morphologically distinct compartments: the inner (fetal) and outer (definitive or adult) zones. Despite considerable effort, the mechanisms that mediate the differential development of the adrenal and gonadal primordia and the fetal and adult adrenal cortices remain incompletely understood. We previously identified a fetal adrenal-specific enhancer (FAdE) in the Ad4BP/SF-1 locus that directs transgene expression to the fetal adrenal cortex and demonstrated that this enhancer is autoregulated by Ad4BP/SF-1. We now combine the FAdE with the Cre/loxP system to trace cell lineages in which the FAdE was active at some stage in development. These lineage-tracing studies establish definitively that the adult cortex derives from precursor cells in the fetal cortex in which the FAdE was activated before the organization into two distinct zones. The potential of these fetal adrenocortical cells to enter the pathway that eventuates in cells of the adult cortex disappeared by embryonic day 14.5. Thus, these studies demonstrate a direct link between the fetal and adult cortices involving a transition that must occur before a specific stage of development.

摘要

核受体Ad4BP/SF-1对于肾上腺皮质和性腺的发育至关重要,而肾上腺皮质和性腺起源于共同的肾上腺生殖嵴原基。肾上腺皮质随后形成形态上不同的部分:内层(胎儿期)和外层(终末或成年期)区域。尽管付出了巨大努力,但介导肾上腺和性腺原基以及胎儿和成年肾上腺皮质差异发育的机制仍未完全了解。我们之前在Ad4BP/SF-1基因座中鉴定出一个胎儿肾上腺特异性增强子(FAdE),它将转基因表达导向胎儿肾上腺皮质,并证明该增强子受Ad4BP/SF-1自身调节。我们现在将FAdE与Cre/loxP系统结合起来,追踪在发育的某个阶段FAdE活跃的细胞谱系。这些谱系追踪研究明确证实,成年皮质起源于胎儿皮质中的前体细胞,在这些细胞组织成两个不同区域之前FAdE就已被激活。这些胎儿肾上腺皮质细胞进入最终形成成年皮质细胞途径的潜能在胚胎第14.5天时消失。因此,这些研究证明了胎儿和成年皮质之间存在直接联系,涉及一个必须在特定发育阶段之前发生的转变。

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