Harland R, Gerhart J
Department of Molecular and Cell Biology, University of California, Berkeley 94720, USA.
Annu Rev Cell Dev Biol. 1997;13:611-67. doi: 10.1146/annurev.cellbio.13.1.611.
The organizer is formed in an equatorial sector of the blastula stage amphibian embryo by cells that have responded to two maternal agents: a general mesoendoderm inducer (involving the TFG-beta signaling pathway) and a dorsal modifier (probably involving the Wnt signaling pathway). The meso-endoderm inducer is secreted by most vegetal cells, those containing maternal materials that had been localized in the vegetal hemisphere of the oocyte during oogenesis. As a consequence of the inducer's distribution and action, the competence domains of prospective ectoderm, mesoderm, and endoderm are established in an animal-to-vegetal order in the blastula. The dorsal modifier signal is secreted by a sector of cells of the animal and vegetal hemispheres on one side of the blastula. These cells contain maternal materials transported there in the first cell cycle from the vegetal pole of the egg along microtubules aligned by cortical rotation. The Nieuwkoop center is the region of blastula cells secreting both maternal signals, and hence specifying the organizer in an equatorial sector. Final steps of organizer formation at the late blastula or early gastrula stage may involve locally secreted zygotic signals as well. At the gastrula stage, the organizer secretes a variety of zygotic proteins that act as antagonists to various members of the BMP and Wnt families of ligands, which are secreted by cells of the competence domains surrounding the organizer. BMPs and Wnts favor ventral development, and cells near the organizer are protected from these agents by the organizer's inducers. The nearby cells are derepressed in their inherent capacity for dorsal development, which is apparent in the neural induction of the ectoderm, dorsalization of the mesoderm, and anteriorization of the endoderm. The organizer also engages in extensive specialized morphogenesis, which brings it within range of responsive cell groups. It also self-differentiates to a variety of axial tissues of the body.
一种是一般的中内胚层诱导因子(涉及转化生长因子-β信号通路),另一种是背侧修饰因子(可能涉及Wnt信号通路)。中内胚层诱导因子由大多数植物极细胞分泌,这些细胞含有在卵子发生过程中定位在卵母细胞植物半球的母体物质。由于诱导因子的分布和作用,原肠胚中预期外胚层、中胚层和内胚层的感受态区域按动物到植物的顺序建立。背侧修饰因子信号由囊胚一侧动物半球和植物半球的一部分细胞分泌。这些细胞含有在第一个细胞周期中从卵的植物极沿着由皮层旋转排列的微管运输到那里的母体物质。nieuwkoop中心是分泌两种母体信号的囊胚细胞区域,因此在赤道区域指定了组织者。在囊胚晚期或原肠胚早期组织者形成的最后步骤可能也涉及局部分泌的合子信号。在原肠胚期,组织者分泌多种合子蛋白,这些蛋白作为BMP和Wnt配体家族各种成员的拮抗剂,这些配体由围绕组织者的感受态区域的细胞分泌。BMP和Wnt有利于腹侧发育,组织者附近的细胞受到组织者诱导因子的保护,免受这些因子的影响。附近的细胞在其固有的背侧发育能力方面被去抑制,这在神经外胚层诱导、中胚层背侧化和内胚层前端化中很明显。组织者还参与广泛的特殊形态发生,使其处于反应性细胞群的范围内。它还自我分化为身体的各种轴向组织。