Daane Jacob M, Enders Allen C, Downs Karen M
Department of Anatomy, University of Wisconsin-Madison, School of Medicine and Public Health, Madison, Wisconsin 53706, USA.
J Morphol. 2011 May;272(5):536-56. doi: 10.1002/jmor.10928. Epub 2011 Jan 31.
The rodent allantois is thought to be unique amongst mammals in not having an endodermal component. Here, we have investigated the mesothelium, or outer surface, of murine umbilical precursor tissue, the allantois (∼7.25-8.5 days postcoitum, dpc) to discover whether it exhibits the properties of an epithelium. A combination of morphology, challenge with biotinylated dextran amines (BDAs), and immunohistochemistry revealed that the mesothelium of the mouse allantois exhibits distinct regional properties. By headfold stages (∼7.75-8.0 dpc), distal mesothelium was generally squamous in shape, and highly permeable to BDA challenge, whereas ventral proximal mesothelium, referred to as "ventral cuboidal mesothelium" (VCM) for the characteristic cuboidal shape of its cells, was relatively impermeable. Although "dorsal cuboidal mesothelium" (DCM) resembled the VCM in cell shape, its permeability to BDA was intermediate between the other two regions. Results of immunostaining for Zonula Occludens-1 (ZO-1) and Epithelial-cadherin (E-cadherin), together with transmission electron microscopy (TEM), suggested that impermeability in the VCM may be due to greater cellular contact area between cells and close packing rather than to maturity of tight junctions, the latter of which, by comparison with the visceral yolk sac, appeared to be rare or absent from the allantoic surface. Both VCM and DCM exhibited an ultrastructure more favorable for protein synthesis than did the distal squamous mesothelium; however, at most stages, VCM exhibited robust afadin (AF-6), whereas the DCM uniquely contained alpha-4-integrin. These observations demonstrate that the allantoic mesothelium is not a conventional epithelium but possesses regional ultrastructural, functional and molecular differences that may play important roles in the correct deployment of the umbilical cord and its associated vascular, hematopoietic, and other cell types.
啮齿动物的尿囊被认为在哺乳动物中是独特的,因为它没有内胚层成分。在这里,我们研究了小鼠脐前体组织——尿囊(交配后约7.25 - 8.5天,dpc)的间皮或外表面,以发现它是否表现出上皮的特性。形态学、生物素化葡聚糖胺(BDA)挑战和免疫组织化学的结合表明,小鼠尿囊的间皮表现出不同的区域特性。在头褶期(约7.75 - 8.0 dpc),远端间皮通常呈鳞状,对BDA挑战具有高渗透性,而腹侧近端间皮,因其细胞呈特征性的立方形而被称为“腹侧立方形间皮”(VCM),则相对不渗透。尽管“背侧立方形间皮”(DCM)在细胞形状上与VCM相似,但其对BDA的渗透性介于其他两个区域之间。紧密连接蛋白-1(ZO-1)和上皮钙黏蛋白(E-钙黏蛋白)免疫染色结果以及透射电子显微镜(TEM)表明,VCM的不渗透性可能是由于细胞间更大的细胞接触面积和紧密堆积,而不是紧密连接的成熟,与内脏卵黄囊相比,后者在尿囊表面似乎很少见或不存在。VCM和DCM都表现出比远端鳞状间皮更有利于蛋白质合成的超微结构;然而,在大多数阶段,VCM表现出强大的afadin(AF-6),而DCM独特地含有α-4整合素。这些观察结果表明,尿囊间皮不是传统的上皮,而是具有区域超微结构、功能和分子差异,这些差异可能在脐带及其相关血管、造血和其他细胞类型的正确部署中发挥重要作用。