年轻和衰老细胞:不同的核f -肌动蛋白模式在拉特库林B诱导

D. Huang
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引用次数: 0

摘要

细胞衰老和细胞骨架都参与了许多疾病和细胞信号通路的形成。尽管最近的研究表明,f -肌动蛋白参与DNA损伤修复、染色质减压、基因转录调控和细胞命运决定。但是关于f -肌动蛋白和衰老的研究仍然缺乏。目前尚不清楚核f -肌动蛋白是否存在于细胞衰老过程中。在这里,通过共聚焦光学切片和延时成像,我们发现肌动蛋白- taggfp2 - nls对研究衰老的人成纤维细胞IMR-90细胞有益。为了诱导细胞核内f -肌动蛋白的组装,我们使用了胞质f -肌动蛋白聚合抑制剂Latrunculin B (latB)。目前尚不清楚年轻细胞和衰老细胞中的核f -肌动蛋白细胞骨架对latB处理的反应是否不同。在这里,latB在年轻和衰老细胞中诱导不同的核f -肌动蛋白模式和动力学。因此,在分析了肌动蛋白动力学结果后,我们证明了latB对年轻和衰老细胞中核f -肌动蛋白细胞骨架的不同影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Young and Senescent Cells: Distinct Nuclear F-actin Patterns Upon Latrunculin B Induction
Both cellular senescence and cytoskeleton are involved in the formation of many diseases and cell signaling pathways. Although recent studies have shown that F-actin is involved in DNA damage repair, chromatin decompression, gene transcription regulation, and cell fate determination. But studies on F-actin and aging are still absence. It is unclear whether nuclear F-actin is present during cellular senescence. Here, by confocal optical sectioning and time-lapse imaging, we found acitn chrommobody-TagGFP2-NLS shows the beneficial on investigating senescent human fibroblast IMR-90 cells. To induce the nuclear F-actin assembly in single cell, we uesd Latrunculin B (latB) which a cytoplasmic F-actin polymerization inhibitor. It is currently unknown whether the nuclear F-actin cytoskeleton in young and senescent cells responds differently to latB treatment. Here, latB application induces distinct nuclear F-actin patterns and dynamics in young and senescent cells. Thus, after analyzing the results of actin dynamic we demonstrate a diverse effect of latB on the nuclear F-actin cytoskeleton in young and senescent cells.
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