Monserrate J P, Brachmann C Baker
Developmental and Cell Biology, University of California Irvine, Irvine, CA 92697, USA.
Cell Death Differ. 2007 Feb;14(2):209-17. doi: 10.1038/sj.cdd.4401947. Epub 2006 May 19.
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.
程序性细胞死亡(PCD)塑造了许多发育中的组织。果蝇视网膜最终的模式形成步骤是在化蛹期间通过PCD消除小眼间晶格细胞的一个子集。目前尚不清楚这个过程是如何在空间上进行调控以确保细胞在正确的位置死亡的。为了解决这个问题,我们实时观察了蛹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。总共有85%的晶格细胞在相邻小眼之间的专属“死亡区”位置死亡。相比之下,与初级色素细胞有特定接触的细胞则受到保护而免于死亡。两种信号通路,即果蝇表皮生长因子受体(dEgfr)和Notch,被认为是调节晶格细胞存活和死亡的核心,但它们不足以建立死亡区。因此,将实时可视化应用于果蝇眼睛为一个动态发育过程提供了新的见解。