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桥粒斑蛋白对于非洲爪蟾胚胎的表皮完整性和形态发生是必需的。

Desmoplakin is required for epidermal integrity and morphogenesis in the Xenopus laevis embryo.

机构信息

Department of Human and Molecular Genetics, Virginia Commonwealth University, 1101 East Marshall St., Richmond, VA 23219, United States; Department of Cell Biology, Emory University School of Medicine, 615 Michael Street Atlanta, GA 30322, United States.

Department of Biology, Virginia Commonwealth University, 1000 West Cary St., Richmond, VA 23284, United States.

出版信息

Dev Biol. 2019 Jun 15;450(2):115-131. doi: 10.1016/j.ydbio.2019.03.010. Epub 2019 Mar 29.

Abstract

Desmoplakin (Dsp) is a unique and critical desmosomal protein, that is integral to epidermal development. However, it is unclear whether this protein is required specifically for epidermal morphogenesis. Using morpholinos or Crispr/Cas9 mutagenesis we decreased the function of Dsp in frog embryos to better understand its role during epidermal development. Dsp morphant and mutant embryos had developmental defects such as epidermal fragility that mimicked what has been reported in mammals. Most importantly, we also uncovered a novel function for Dsp in the morphogenesis of the epidermis in X. laevis. In particular, Dsp is required during the process of radial intercalation where basally located cells move into the outer epidermal layer. Once inserted these newly intercalated cells expand their apical surface and then they differentiate into specific epidermal cell types. Decreased levels of Dsp resulted in the failure of the radially intercalating cells to expand their apical surface, thereby reducing the number of differentiated multiciliated and secretory cells. Such defects correlate with changes in E-cadherin levels and actin and microtubule localization which could explain the defects in apical expansion. A mutated form of Dsp that maintains cell-cell adhesion but eliminates the connections to the cytoskeleton results in the same epidermal morphogenesis defect. These results suggest a specific role for Dsp in the apical expansion of cells during radial intercalation. We have developed a novel system, in the frog, to demonstrate for the first time that desmosomes not only protect against mechanical stress but are also critical for epidermal morphogenesis.

摘要

桥粒斑蛋白(Dsp)是一种独特且关键的桥粒蛋白,对于表皮发育是不可或缺的。然而,目前尚不清楚该蛋白是否专门用于表皮形态发生。我们使用形态发生抑制物或 Crispr/Cas9 诱变技术降低了青蛙胚胎中 Dsp 的功能,以更好地了解其在表皮发育过程中的作用。Dsp 形态发生抑制物和突变体胚胎存在表皮脆弱等发育缺陷,这与哺乳动物的报道类似。最重要的是,我们还揭示了 Dsp 在 X. laevis 表皮形态发生中的一个新功能。具体而言,Dsp 在径向插入过程中是必需的,在这个过程中,基底细胞移动到表皮外层。一旦插入,这些新插入的细胞会扩大它们的顶端表面,然后分化成特定的表皮细胞类型。Dsp 水平降低会导致径向插入细胞无法扩大其顶端表面,从而减少分化的多纤毛和分泌细胞的数量。这些缺陷与 E-钙粘蛋白水平以及肌动蛋白和微管定位的变化相关,这可以解释顶端扩张的缺陷。保留细胞间黏附但消除与细胞骨架连接的 Dsp 突变体导致相同的表皮形态发生缺陷。这些结果表明 Dsp 在径向插入过程中细胞顶端扩张中的特定作用。我们在青蛙中开发了一种新系统,首次证明了桥粒不仅可以抵抗机械应激,而且对于表皮形态发生也是至关重要的。

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