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机械信号调节 TAZ 活性介导的细胞特化中的侧向抑制。

Lateral Inhibition in Cell Specification Mediated by Mechanical Signals Modulating TAZ Activity.

机构信息

Institute of Science and Technology Austria, 3400 Klosterneuburg, Austria.

Institute of Science and Technology Austria, 3400 Klosterneuburg, Austria.

出版信息

Cell. 2019 Mar 7;176(6):1379-1392.e14. doi: 10.1016/j.cell.2019.01.019. Epub 2019 Feb 14.

Abstract

Cell fate specification by lateral inhibition typically involves contact signaling through the Delta-Notch signaling pathway. However, whether this is the only signaling mode mediating lateral inhibition remains unclear. Here we show that in zebrafish oogenesis, a group of cells within the granulosa cell layer at the oocyte animal pole acquire elevated levels of the transcriptional coactivator TAZ in their nuclei. One of these cells, the future micropyle precursor cell (MPC), accumulates increasingly high levels of nuclear TAZ and grows faster than its surrounding cells, mechanically compressing those cells, which ultimately lose TAZ from their nuclei. Strikingly, relieving neighbor-cell compression by MPC ablation or aspiration restores nuclear TAZ accumulation in neighboring cells, eventually leading to MPC re-specification from these cells. Conversely, MPC specification is defective in taz follicles. These findings uncover a novel mode of lateral inhibition in cell fate specification based on mechanical signals controlling TAZ activity.

摘要

通过侧向抑制来决定细胞命运通常涉及通过 Delta-Notch 信号通路进行接触信号传递。然而,这种信号模式是否是介导侧向抑制的唯一模式尚不清楚。在这里,我们发现在斑马鱼卵母细胞发生过程中,卵母细胞动物极的颗粒细胞层中的一组细胞在其核内获得转录共激活因子 TAZ 的水平升高。其中一个细胞,未来的卵孔前体细胞 (MPC),核内 TAZ 的积累水平越来越高,并且比其周围的细胞生长得更快,通过机械压缩这些细胞,最终导致这些细胞的核内失去 TAZ。引人注目的是,通过 MPC 消融或抽吸消除邻接细胞的压缩,会恢复邻接细胞中核 TAZ 的积累,最终导致这些细胞中 MPC 的重新特化。相反,taz 滤泡中的 MPC 特化缺陷。这些发现揭示了一种基于控制 TAZ 活性的机械信号的新的细胞命运特化的侧向抑制模式。

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