Moury J D, Jacobson A G
Department of Zoology, University of Texas, Austin 78712-1064.
Dev Biol. 1989 May;133(1):44-57. doi: 10.1016/0012-1606(89)90295-9.
According to a recent model, the cortical tractor model, neural fold and neural crest formation occurs at the boundary between neural plate and epidermis because random cell movements become organized at this site. If this is correct, then a fold should form at any boundary between epidermis and neural plate. To test that proposition, we created new boundaries in axolotl embryos by juxtaposing pieces of neural plate and epidermis that would not normally participate in fold formation. These boundaries were examined superficially and histologically for the presence of folds, permitting the following observations. Folds form at each newly created boundary, and as many folds form as there are boundaries. When two folds meet they fuse into a hollow "tube" of neural tissue covered by epidermis. Sections reveal that these ectopic folds and "tubes" are morphologically similar to their natural counterparts. Transplanting neural plate into epidermis produces nodules of neural tissue with central lumens and peripheral nerve fibers, and transplanting epidermis into neural plate causes the neural tube and the dorsal fin to bifurcate in the region of the graft. Tissue transplanted homotypically as a control integrates into the host tissue without forming folds. When tissue from a pigmented embryo is transplanted into an albino host, the presence of pigment allows the donor cells to be distinguished from those of the host. Mesenchymal cells and melanocytes originating from neural plate transplants indicate that neural crest cells form at these new boundaries. Thus, any boundary between neural plate and epidermis denotes the site of a neural fold, and the behavior of cells at this boundary appears to help fold the epithelium. Since folds can form in ectopic locations on an embryo, local interactions rather than classical neural induction appear to be responsible for the formation of neural folds and neural crest.
根据最近的一种模型,即皮质牵引模型,神经褶和神经嵴的形成发生在神经板和表皮之间的边界处,因为随机的细胞运动在这个部位变得有组织。如果这是正确的,那么在表皮和神经板之间的任何边界处都应该形成一个褶。为了验证这一命题,我们通过将通常不会参与褶形成的神经板和表皮碎片并列放置,在蝾螈胚胎中创建了新的边界。对这些边界进行了表面和组织学检查以寻找褶的存在,从而得出以下观察结果。在每个新创建的边界处都会形成褶,并且形成的褶的数量与边界的数量相同。当两个褶相遇时,它们会融合成一个由表皮覆盖的神经组织空心“管”。切片显示,这些异位褶和“管”在形态上与其天然对应物相似。将神经板移植到表皮中会产生具有中央管腔和外周神经纤维的神经组织结节,而将表皮移植到神经板中会导致神经管和背鳍在移植区域分叉。作为对照,同种同型移植的组织会整合到宿主组织中而不形成褶。当将来自有色胚胎的组织移植到白化病宿主中时,色素的存在使得供体细胞能够与宿主细胞区分开来。源自神经板移植的间充质细胞和黑素细胞表明神经嵴细胞在这些新边界处形成。因此,神经板和表皮之间的任何边界都表示神经褶的位置,并且该边界处细胞的行为似乎有助于上皮细胞折叠。由于褶可以在胚胎的异位位置形成,局部相互作用而非经典的神经诱导似乎是神经褶和神经嵴形成的原因。