在THP-1单核细胞向巨噬细胞分化过程中,输入蛋白水平的变化促进核蛋白酶体降解细胞周期相关蛋白。

IF 3.5 4区 生物学 Q1 Biochemistry, Genetics and Molecular Biology
Makoto Kimura, Yutaka Ogawa, Shoko Motohashi, Naoko Imamoto
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引用次数: 0

摘要

输入蛋白家族核细胞质转运受体共享数千种货物蛋白。为了阐明通过转运调控的细胞调控机制,我们通过western blotting分析了转运受体的水平,并使用质谱法定量了THP-1细胞单核细胞向巨噬细胞分化过程中的总细胞蛋白和核蛋白。在分化过程中,输入蛋白α1减少,输入蛋白α5增加。细胞周期相关蛋白在全细胞和细胞核中均减少,蛋白酶体相关蛋白在细胞核中增加,但在全细胞中没有增加。在输入蛋白-α1过表达的分化过程中,细胞核内部分细胞分裂相关蛋白水平恢复,输入蛋白-α5敲低导致细胞核内蛋白酶体组装因子减少。在这种分化中,转运受体通过减少输入和促进核蛋白酶体降解来减少不必要的核蛋白。这项研究证明了核转运控制在细胞调控中的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Changes in importin levels promote nuclear proteasomal degradation of cell cycle-related proteins during THP-1 monocyte-to-macrophage differentiation

Changes in importin levels promote nuclear proteasomal degradation of cell cycle-related proteins during THP-1 monocyte-to-macrophage differentiation

Importin family nucleocytoplasmic transport receptors share thousands of cargo proteins. To elucidate cell regulatory mechanisms via transport regulation, we analyzed the levels of transport receptors by western blotting and quantified the total cellular and nuclear proteins during monocyte-to-macrophage differentiation of THP-1 cells using mass spectrometry. Importin-α1 decreased and importin-α5 increased during the differentiation. Cell cycle-related proteins decreased in both whole cells and nuclei, and proteasome-related proteins increased in the nuclei but not in whole cells. During the differentiation with importin-α1 overexpression, the nuclear levels of some cell division-related proteins recovered, and with importin-α5 knockdown, proteasome assembly factors decreased in the nuclei. In this differentiation, transport receptors reduce unnecessary nuclear proteins by abating import and promoting nuclear proteasomal degradation. This study demonstrates the importance of global nuclear transport control in cell regulation.

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来源期刊
FEBS Letters
FEBS Letters 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
303
审稿时长
1.0 months
期刊介绍: FEBS Letters is one of the world''s leading journals in molecular biology and is renowned both for its quality of content and speed of production. Bringing together the most important developments in the molecular biosciences, FEBS Letters provides an international forum for Minireviews, Research Letters and Hypotheses that merit urgent publication.
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