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p120ctn 介导的器官模式形成先于并决定胰腺祖细胞命运。

p120ctn-Mediated Organ Patterning Precedes and Determines Pancreatic Progenitor Fate.

机构信息

Novo Nordisk Foundation Center for Stem Cell Biology (Danstem), University of Copenhagen, 2200 Copenhagen N, Denmark.

Novo Nordisk Foundation Center for Stem Cell Biology (Danstem), University of Copenhagen, 2200 Copenhagen N, Denmark.

出版信息

Dev Cell. 2019 Apr 8;49(1):31-47.e9. doi: 10.1016/j.devcel.2019.02.005. Epub 2019 Mar 7.

Abstract

The mechanism of how organ shape emerges and specifies cell fate is not understood. Pancreatic duct and endocrine lineages arise in a spatially distinct domain from the acinar lineage. Whether these lineages are pre-determined or settle once these niches have been established remains unknown. Here, we reconcile these two apparently opposing models, demonstrating that pancreatic progenitors re-localize to establish the niche that will determine their ultimate fate. We identify a p120ctn-regulated mechanism for coordination of organ architecture and cellular fate mediated by differential E-cadherin based cell sorting. Reduced p120ctn expression is necessary and sufficient to re-localize a subset of progenitors to the peripheral tip domain, where they acquire an acinar fate. The same mechanism is used re-iteratively during endocrine specification, where it balances the choice between the alpha and beta cell fates. In conclusion, organ patterning is regulated by p120ctn-mediated cellular positioning, which precedes and determines pancreatic progenitor fate.

摘要

器官形态如何出现和指定细胞命运的机制尚不清楚。胰腺导管和内分泌谱系从腺泡谱系在空间上不同的区域出现。这些谱系是预先确定的,还是一旦这些龛位建立后就确定下来,目前还不得而知。在这里,我们调和了这两种明显对立的模型,证明胰腺祖细胞重新定位以建立决定其最终命运的龛位。我们确定了一个由 p120ctn 调节的机制,用于协调器官结构和细胞命运,该机制通过基于 E-钙粘蛋白的细胞分选的差异来介导。降低 p120ctn 的表达对于将祖细胞的一部分重新定位到外周尖端区域是必要的,在那里它们获得腺泡命运。在内分泌特化过程中,同样的机制被反复使用,在该过程中,它平衡了 alpha 和 beta 细胞命运之间的选择。总之,器官形态发生受 p120ctn 介导的细胞定位调节,该定位先于并决定胰腺祖细胞命运。

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