Sheth B, Fontaine J J, Ponza E, McCallum A, Page A, Citi S, Louvard D, Zahraoui A, Fleming T P
Division of Cell Sciences, School of Biological Sciences, University of Southampton, Bassett Crescent East, SO16 7PX, Southampton, UK.
Mech Dev. 2000 Oct;97(1-2):93-104. doi: 10.1016/s0925-4773(00)00416-0.
We have investigated the mechanisms by which the epithelial apicolateral junctional complex (AJC) is generated during trophectoderm differentiation in the mouse blastocyst using molecular, structural and functional analyses. The mature AJC comprises an apical tight junction (TJ), responsible for intercellular sealing and blastocoel formation, and subjacent zonula adherens E-cadherin/catenin adhesion complex which also extends along lateral membrane contact sites. Dual labelling confocal microscopy revealed that the AJC derived from a single 'intermediate' complex formed following embryo compaction at the 8-cell stage in which the TJ-associated peripheral membrane protein, ZO-1alpha- isoform, was co-localized with both alpha- and beta-catenin. However, following assembly of the TJ transmembrane protein, occludin, from the early 32-cell stage when blastocoel formation begins, ZO-1alpha- and other TJ proteins (ZO-1alpha+ isoform, occludin, cingulin) co-localized in an apical TJ which was separate from a subjacent E-cadherin/catenin zonula adherens complex. Thin-section electron microscopy confirmed that a single zonula adherens-like junctional complex present at the AJC site following compaction matured into a dual TJ and zonula adherens complex at the blastocyst stage. Embryo incubation in the tracer FITC-dextran 4 kDa showed that a functional TJ seal was established coincident with blastocoel formation. We also found that rab13, a small GTPase previously localized to the TJ, is expressed at all stages of preimplantation development and relocates from the cytoplasm to the site of AJC biogenesis from compaction onwards with rab13 and ZO-1alpha- co-localizing precisely. Our data indicate that the segregation of the two elements of the AJC occurs late in trophectoderm differentiation and likely has functional importance in blastocyst formation. Moreover, we propose a role for rab13 in the specification of the AJC site and the formation and segregation of the TJ.
我们利用分子、结构和功能分析方法,研究了小鼠囊胚滋养外胚层分化过程中上皮顶侧连接复合体(AJC)形成的机制。成熟的AJC由负责细胞间密封和囊胚腔形成的顶端紧密连接(TJ)以及下方的黏着小带E-钙黏蛋白/连环蛋白黏附复合体组成,该复合体也沿着侧膜接触位点延伸。双重标记共聚焦显微镜显示,AJC源自8细胞期胚胎致密化后形成的单个“中间”复合体,其中与TJ相关的外周膜蛋白ZO-1α异构体与α-连环蛋白和β-连环蛋白共定位。然而,从囊胚腔形成开始的早期32细胞期TJ跨膜蛋白闭合蛋白组装后,ZO-1α和其他TJ蛋白(ZO-1α +异构体、闭合蛋白、cingulin)在顶端TJ中共定位,该顶端TJ与下方的E-钙黏蛋白/连环蛋白黏着小带复合体分开。超薄切片电子显微镜证实,致密化后在AJC位点存在的单个黏着小带样连接复合体在囊胚期成熟为双重TJ和黏着小带复合体。用示踪剂FITC-葡聚糖4 kDa孵育胚胎表明,功能性TJ密封与囊胚腔形成同时建立。我们还发现,小GTP酶rab13先前定位于TJ,在植入前发育的所有阶段均有表达,从致密化开始从细胞质重新定位到AJC生物发生位点,rab13和ZO-1α精确共定位。我们的数据表明,AJC的两个元件的分离发生在滋养外胚层分化后期,可能在囊胚形成中具有功能重要性。此外,我们提出rab13在AJC位点的特化以及TJ的形成和分离中发挥作用。