Reuter R, Grunewald B, Leptin M
Max-Planck-Institut für Entwicklungsbiologie, Tübingen, FR Germany.
Development. 1993 Dec;119(4):1135-45. doi: 10.1242/dev.119.4.1135.
The endodermal midgut arises from two primordia, the anterior midgut (AMG) primordium and the posterior midgut (PMG) primordium, which are separated by almost the entire length of the Drosophila embryo. To form the midgut, these two parts have to extend towards each other and to fuse laterally on both sides of the yolk. Shortly before and during that movement, AMG and PMG are arranged as mesenchymal cell masses, but later the midgut cells form an epithelium. We show that these two aspects of midgut development, migration of AMG and PMG and transition to an epithelium, depend on the mesoderm. The extension of the midgut primordia is achieved by cell migration along the visceral mesoderm which forms a continuous layer of cells within the germ band. In mutant embryos lacking the entire mesoderm or failing to differentiate the visceral mesoderm, AMG and PMG are formed but do not migrate properly. In addition, they fail to form an epithelium and instead either remain as compact cell masses anterior and posterior to the yolk (in twist and snail mutant embryos) or only occasionally wrap around the yolk before embryogenesis is completed (in tinman-deficient embryos). We conclude that the visceral mesoderm serves as a substratum for the migrating endodermal cells and that the contact between visceral mesoderm and endoderm is required for the latter to become an epithelium.
内胚层中肠起源于两个原基,即前中肠(AMG)原基和后中肠(PMG)原基,它们在果蝇胚胎的几乎整个长度上相互分隔。为了形成中肠,这两个部分必须相互延伸并在卵黄两侧横向融合。在该运动之前不久及运动过程中,AMG和PMG以间充质细胞团的形式排列,但后来中肠细胞形成上皮。我们发现中肠发育的这两个方面,即AMG和PMG的迁移以及向上皮的转变,依赖于中胚层。中肠原基的延伸是通过细胞沿着内脏中胚层迁移实现的,内脏中胚层在胚带内形成连续的细胞层。在缺乏整个中胚层或无法分化内脏中胚层的突变胚胎中,AMG和PMG形成但不能正常迁移。此外,它们无法形成上皮,而是要么在卵黄前后保持为紧密的细胞团(在twist和snail突变胚胎中),要么在胚胎发育完成前仅偶尔包裹卵黄(在tinman缺陷胚胎中)。我们得出结论,内脏中胚层作为迁移的内胚层细胞的基质,内脏中胚层与内胚层之间的接触是后者形成上皮所必需的。