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Identification of the death zone: a spatially restricted region for programmed cell death that sculpts the fly eye.

机译:识别死亡区:雕刻蝇眼的程序性细胞死亡的空间受限区域。

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摘要

Programmed cell death (PCD) sculpts many developing tissues. The final patterning step of the Drosophila retina is the elimination, through PCD, of a subset of interommatidial lattice cells during pupation. It is not understood how this process is spatially regulated to ensure that cells die in the proper positions. To address this, we observed PCD of lattice cells in the pupal retina in real time. This live-visualization method demonstrates that lattice cell apoptosis is a highly specific process. In all, 85% of lattice cells die in exclusive 'death zone' positions between adjacent ommatidia. In contrast, cells that make specific contacts with primary pigment cells are protected from death. Two signaling pathways, Drosophila epidermal growth factor receptor (dEgfr) and Notch, that are thought to be central to the regulation of lattice cell survival and death, are not sufficient to establish the death zone. Thus, application of live visualization to the fly eye gives new insight into a dynamic developmental process.
机译:程序性细胞死亡(PCD)雕刻许多发育中的组织。果蝇视网膜的最后构图步骤是化脓期间通过PCD消除了一部分间质细胞。还不知道如何在空间上调节该过程以确保细胞在适当的位置死亡。为了解决这个问题,我们实时观察了p视网膜中晶格细胞的PCD。这种实时可视化方法表明晶格细胞凋亡是一个高度特异性的过程。总计,有85%的晶格细胞死于相邻眼病之间唯一的“死亡区”位置。相反,与原代色素细胞发生特定接触的细胞被保护免受死亡。果蝇表皮生长因子受体(dEgfr)和Notch这两个信号通路被认为是调节晶格细胞存活和死亡的关键,不足以建立死亡区。因此,实时可视化在蝇眼中的应用为动态发展过程提供了新的见识。

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