TNF-α驱动的极化EGF受体运输变化促进了MDCK上皮细胞顶端表面磷脂酰肌醇3-激酶/蛋白激酶B的信号传导。

IF 2.5 3区 生物学 Q3 CELL BIOLOGY
Traffic Pub Date : 2025-04-01 DOI:10.1111/tra.70005
Syntyche Ngalula, Cathleen R Carlin
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引用次数: 0

摘要

本文描述了一种新的非常规分泌途径,该途径促进了极化上皮细胞对免疫细胞介质反应的根尖膜上的EGF受体(EGFR)信号传导。上皮组织在我们的身体和外部环境之间提供了一个物理屏障,并与循环细胞和局部免疫细胞有着密切的关系。我们的研究描述了促炎细胞因子肿瘤坏死因子-α (TNF-α)和EGFR之间意想不到的联系,通常定位于极化上皮细胞的基底外膜。这两种分子位于复杂的生物网络之上,从信号通路相互作用的角度来看,它们有着悠久的共同研究兴趣。我们发现TNF-α通过改变EGFR分泌的速度和方向来改变完全极化上皮细胞的功能景观。我们的研究结果表明,顶端EGFR在重新合成的几分钟内就可以通过内质网的直接途径传递,而不需要通过高尔基体复合体。此外,我们的研究表明,顶端细胞区隔化是通过磷脂酰肌醇-4,5-二磷酸3-激酶/蛋白激酶-b途径指定EGFR信号传导的重要机制。我们的研究为更好地理解炎症细胞因子如何通过改变上皮细胞信号系统的空间组织来微调局部稳态和炎症反应铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TNF-α-Driven Changes in Polarized EGF Receptor Trafficking Facilitate Phosphatidylinositol 3-Kinase/Protein Kinase B Signaling From the Apical Surface of MDCK Epithelial Cells.

This manuscript describes a novel unconventional secretory pathway that facilitates EGF receptor (EGFR) signaling from apical membranes in polarized epithelial cells responding to immune cell mediators. Epithelial tissues provide a physical barrier between our bodies and the external environment and share an intimate relationship with circulating and local immune cells. Our studies describe an unexpected connection between the proinflammatory cytokine tumor necrosis factor-alpha (TNF-α) and EGFR typically localized to basolateral membranes in polarized epithelial cells. These two molecules sit atop complex biological networks with a long history of shared investigative interest from the vantage point of signaling pathway interactions. We have discovered that TNF-α alters the functional landscape of fully polarized epithelial cells by changing the speed and direction of EGFR secretion. Our results show apical EGFR delivery occurs within minutes of de novo synthesis likely via a direct route from the endoplasmic reticulum without passage through the Golgi complex. Additionally, our studies have revealed that apical cellular compartmentalization constitutes an important mechanism to specify EGFR signaling via phosphatidylinositol-4,5-bisphosphate 3-kinase/protein-kinase-B pathways. Our study paves the way for a better understanding of how inflammatory cytokines fine-tune local homeostatic and inflammatory responses by altering the spatial organization of epithelial cell signaling systems.

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来源期刊
Traffic
Traffic 生物-细胞生物学
CiteScore
8.10
自引率
2.20%
发文量
50
审稿时长
2 months
期刊介绍: Traffic encourages and facilitates the publication of papers in any field relating to intracellular transport in health and disease. Traffic papers span disciplines such as developmental biology, neuroscience, innate and adaptive immunity, epithelial cell biology, intracellular pathogens and host-pathogen interactions, among others using any eukaryotic model system. Areas of particular interest include protein, nucleic acid and lipid traffic, molecular motors, intracellular pathogens, intracellular proteolysis, nuclear import and export, cytokinesis and the cell cycle, the interface between signaling and trafficking or localization, protein translocation, the cell biology of adaptive an innate immunity, organelle biogenesis, metabolism, cell polarity and organization, and organelle movement. All aspects of the structural, molecular biology, biochemistry, genetics, morphology, intracellular signaling and relationship to hereditary or infectious diseases will be covered. Manuscripts must provide a clear conceptual or mechanistic advance. The editors will reject papers that require major changes, including addition of significant experimental data or other significant revision. Traffic will consider manuscripts of any length, but encourages authors to limit their papers to 16 typeset pages or less.
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