Cellular Distribution Pattern of tjp1 (ZO-1) in Xenopus laevis Oocytes Heterologously Expressing Claudins.

IF 2.3 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nora Brunner, Laura Stein, Salah Amasheh
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引用次数: 4

Abstract

Epithelial barriers constitute a fundamental requirement in every organism, as they allow the separation of different environments and set boundaries against noxious and other adverse effectors. In many inflammatory and degenerative diseases, epithelial barrier function is impaired because of a disturbance of the paracellular seal. Recently, the Xenopus laevis oocyte has been established as a heterologous expression model for the analysis of transmembrane tight junction protein interactions and is currently considered to be a suitable screening model for barrier effectors. A prerequisite for this application is a physiological anchoring of claudins to the cytoskeleton via the major scaffolding protein tjp1 (tight junction protein 1, ZO-1). We have analyzed the oocyte model with regard to the interaction of heterologously expressed claudins and tjp1. Our experiments have revealed endogenous tjp1 expression in protein and mRNA analyses of unfertilized Xenopus laevis oocytes expressing human claudin 1 (CLDN1) to claudin 5 (CLDN5). The amphibian cell model can therefore be used for the analysis of claudin interactions.

Abstract Image

Abstract Image

Abstract Image

tjp1 (ZO-1)在异源表达claudin的非洲爪蟾卵母细胞中的细胞分布模式
上皮屏障是每个生物体的基本要求,因为它们允许不同环境的分离,并设置对有害和其他不利影响的边界。在许多炎性和退行性疾病中,上皮屏障功能受损是由于细胞旁封闭的紊乱。近年来,非洲爪蟾卵母细胞被建立为分析跨膜紧密连接蛋白相互作用的异源表达模型,目前被认为是一种合适的屏障效应物筛选模型。此应用的先决条件是通过主要的支架蛋白tjp1(紧密连接蛋白1,ZO-1)将claudin生理锚定到细胞骨架上。我们分析了异源表达的claudin与tjp1相互作用的卵母细胞模型。我们的实验揭示了内源性tjp1在表达人CLDN1到CLDN5的未受精非洲爪蟾卵母细胞中的蛋白和mRNA表达。因此,两栖动物细胞模型可用于分析claudin相互作用。
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来源期刊
Journal of Membrane Biology
Journal of Membrane Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
4.20%
发文量
63
审稿时长
6-12 weeks
期刊介绍: The Journal of Membrane Biology is dedicated to publishing high-quality science related to membrane biology, biochemistry and biophysics. In particular, we welcome work that uses modern experimental or computational methods including but not limited to those with microscopy, diffraction, NMR, computer simulations, or biochemistry aimed at membrane associated or membrane embedded proteins or model membrane systems. These methods might be applied to study topics like membrane protein structure and function, membrane mediated or controlled signaling mechanisms, cell-cell communication via gap junctions, the behavior of proteins and lipids based on monolayer or bilayer systems, or genetic and regulatory mechanisms controlling membrane function. Research articles, short communications and reviews are all welcome. We also encourage authors to consider publishing ''negative'' results where experiments or simulations were well performed, but resulted in unusual or unexpected outcomes without obvious explanations. While we welcome connections to clinical studies, submissions that are primarily clinical in nature or that fail to make connections to the basic science issues of membrane structure, chemistry and function, are not appropriate for the journal. In a similar way, studies that are primarily descriptive and narratives of assays in a clinical or population study are best published in other journals. If you are not certain, it is entirely appropriate to write to us to inquire if your study is a good fit for the journal.
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