受体介导的内化以RAB4和RAB5依赖的方式促进内体大小和数量的增加。

IF 4.5 3区 生物学 Q2 CELL BIOLOGY European journal of cell biology Pub Date : 2023-09-01 DOI:10.1016/j.ejcb.2023.151339
Naava Naslavsky , Steve Caplan
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引用次数: 0

摘要

尽管早期/分选内体(EE/SE)在细胞中受体介导的内化和持续的信号转导中具有重要意义,但其特征仍不完全,围绕其大小和数量的动力学存在许多悬而未决的问题。虽然有几项研究报告了内吞事件导致EE/SE大小和数量的增加,但很少有研究以方法和定量的方式处理这种动态。在此,我们应用定量荧光显微镜来测量两种不同配体(转铁蛋白和表皮生长因子)内化后EE/SE的大小和数量。此外,我们使用siRNA敲除来确定5种不同的内体RAB蛋白(RAB4、RAB5、RAB8A、RAB10和RAB11A)在EE/SE动力学中的参与。我们的研究为内吞过程中内体的动力学提供了新的信息,为研究受体介导的内化和内吞事件的研究人员提供了重要参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Receptor-mediated internalization promotes increased endosome size and number in a RAB4- and RAB5-dependent manner

Despite their significance in receptor-mediated internalization and continued signal transduction in cells, early/sorting endosomes (EE/SE) remain incompletely characterized, with many outstanding questions that surround the dynamics of their size and number. While several studies have reported increases in EE/SE size and number resulting from endocytic events, few studies have addressed such dynamics in a methodological and quantitative manner. Herein we apply quantitative fluorescence microscopy to measure the size and number of EE/SE upon internalization of two different ligands: transferrin and epidermal growth factor. Additionally, we used siRNA knock-down to determine the involvement of 5 different endosomal RAB proteins (RAB4, RAB5, RAB8A, RAB10 and RAB11A) in EE/SE dynamics. Our study provides new information on the dynamics of endosomes during endocytosis, an important reference for researchers studying receptor-mediated internalization and endocytic events.

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来源期刊
European journal of cell biology
European journal of cell biology 生物-细胞生物学
CiteScore
7.30
自引率
1.50%
发文量
80
审稿时长
38 days
期刊介绍: The European Journal of Cell Biology, a journal of experimental cell investigation, publishes reviews, original articles and short communications on the structure, function and macromolecular organization of cells and cell components. Contributions focusing on cellular dynamics, motility and differentiation, particularly if related to cellular biochemistry, molecular biology, immunology, neurobiology, and developmental biology are encouraged. Manuscripts describing significant technical advances are also welcome. In addition, papers dealing with biomedical issues of general interest to cell biologists will be published. Contributions addressing cell biological problems in prokaryotes and plants are also welcome.
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