Schlichting Karin, Dahmann Christian
Max Planck Institute of Molecular Cell Biology and Genetics, Pfotenhauerstrasse 108, 01307 Dresden, Germany.
Mech Dev. 2008 Aug;125(8):712-28. doi: 10.1016/j.mod.2008.04.005. Epub 2008 Apr 27.
During Drosophila eye development, cell differentiation is preceded by the formation of a morphogenetic furrow, which progresses across the epithelium from posterior to anterior. Cells within the morphogenetic furrow are apically constricted and shortened along their apical-basal axis. However, how these cell shape changes and, thus, the progression of the morphogenetic furrow are controlled is not well understood. Here we show that cells simultaneously lacking Hedgehog and Dpp signal transduction fail to shorten and do not enter the morphogenetic furrow. Moreover, we have identified a gene, cadherin Cad86C, which is highly expressed in cells of the leading flank of the morphogenetic furrow. Ectopic activation of either the Hedgehog or Dpp signal transduction pathway results in elevated Cad86C expression. Conversely, simultaneous loss of both Hedgehog and Dpp signal transduction leads to decreased Cad86C expression. Finally, ectopic expression of Cad86C in either eye-antennal imaginal discs or wing imaginal discs results in apical constriction and shortening of cells. We conclude that Hedgehog and Dpp signaling promote the shortening of cells within the morphogenetic furrow. Induction of Cad86C expression might be one mechanism through which Hedgehog and Dpp promote these cell shape changes.
在果蝇眼睛发育过程中,细胞分化之前会形成形态发生沟,该沟从上皮组织的后部向前部推进。形态发生沟内的细胞顶端收缩,并沿其顶-基轴缩短。然而,这些细胞形状变化以及形态发生沟的推进是如何被控制的,目前还不太清楚。在这里,我们表明同时缺乏Hedgehog和Dpp信号转导的细胞无法缩短,也不会进入形态发生沟。此外,我们鉴定出一个基因,钙黏蛋白Cad86C,它在形态发生沟前缘的细胞中高度表达。Hedgehog或Dpp信号转导途径的异位激活会导致Cad86C表达升高。相反,Hedgehog和Dpp信号转导同时缺失会导致Cad86C表达降低。最后,在眼-触角成虫盘或翅成虫盘中异位表达Cad86C会导致细胞顶端收缩和缩短。我们得出结论,Hedgehog和Dpp信号传导促进形态发生沟内细胞的缩短。Cad86C表达的诱导可能是Hedgehog和Dpp促进这些细胞形状变化的一种机制。