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出生时间研究重塑了脑垂体细胞特化的模型。

Birthdating studies reshape models for pituitary gland cell specification.

机构信息

Department of Human Genetics, University of Michigan Medical School, 4909 Buhl Building, 1241 East Catherine Street, Ann Arbor, MI 48109-5618, USA.

出版信息

Dev Biol. 2011 Apr 15;352(2):215-27. doi: 10.1016/j.ydbio.2011.01.010. Epub 2011 Jan 22.

Abstract

The intermediate and anterior lobes of the pituitary gland are derived from an invagination of oral ectoderm that forms Rathke's pouch. During gestation proliferating cells are enriched around the pouch lumen, and they appear to delaminate as they exit the cell cycle and differentiate. During late mouse gestation and the postnatal period, anterior lobe progenitors re-enter the cell cycle and expand the populations of specialized, hormone-producing cells. At birth, all cell types are present, and their localization appears stratified based on cell type. We conducted a birth dating study of Rathke's pouch derivatives to determine whether the location of specialized cells at birth is correlated with the timing of cell cycle exit. We find that all of the anterior lobe cell types initiate differentiation concurrently with a peak between e11.5 and e13.5. Differentiation of intermediate lobe melanotropes is delayed relative to anterior lobe cell types. We discovered that specialized cell types are not grouped together based on birth date and are dispersed throughout the anterior lobe. Thus, the apparent stratification of specialized cells at birth is not correlated with cell cycle exit. Thus, the currently popular model of cell specification, dependent upon timing of extrinsic, directional gradients of signaling molecules, needs revision. We propose that signals intrinsic to Rathke's pouch are necessary for cell specification between e11.5 and e13.5 and that cell-cell communication likely plays an important role in regulating this process.

摘要

垂体的中间和前叶是由口腔外胚层的内陷形成的 Rathke 囊。在妊娠期间,增殖细胞在囊腔周围富集,并且当它们退出细胞周期并分化时,似乎会分层。在晚期小鼠妊娠和出生后期间,前叶祖细胞重新进入细胞周期并扩大了专门的激素产生细胞的群体。出生时,所有细胞类型都存在,并且它们的定位似乎根据细胞类型分层。我们对 Rathke 囊衍生物进行了出生日期研究,以确定专门细胞在出生时的位置是否与细胞周期退出的时间相关。我们发现,所有前叶细胞类型都与 e11.5 和 e13.5 之间的峰值同时开始分化。中间叶黑素细胞的分化相对于前叶细胞类型延迟。我们发现,专门的细胞类型不是根据出生日期分组的,而是分散在前叶中。因此,出生时专门细胞的明显分层与细胞周期退出无关。因此,目前流行的细胞特化模型,依赖于信号分子的外在、定向梯度的时间,需要修订。我们提出,Rathke 囊内的信号对于 e11.5 和 e13.5 之间的细胞特化是必要的,并且细胞间通信可能在调节这个过程中发挥重要作用。

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