Bax- Bcl-xL interaction dynamics during the progression of cell cycle and cell death using FLIM-FRET.

IF 3 Q2 CELL BIOLOGY
Cell Stress Pub Date : 2025-07-08 eCollection Date: 2025-01-01 DOI:10.15698/cst2025.07.307
Aman M Halikar, Aneesh Chandrasekharan, Asha Lekshmi, Aswathy Sivasailam, Jain Tiffee P J, Shivanshu K Tiwari, Aijaz Ahmad Rather, T R Santhoshkumar
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引用次数: 0

Abstract

Genetically identical cells in a population show cell-to-cell variability because of fluctuation in transcription, epigenetics, post-translational modifications, and stochastic or extrinsically triggered non-genetic alterations. The change in the interaction state of proteins also emerges as an additional layer of cell signaling that influences cell cycle and cell death. However, the interrelation between cell cycle progression and cell death under the influence of spatio-temporal changes in protein-protein interaction is difficult to demonstrate in growing cells. This requires tools for cell cycle phase-resolved visualization of macromolecular interactions in live cells. We describe an approach to visualize the interaction of pro- and anti-death signaling partners, Bax and Bcl-xL, during cell cycle progression and cell death in live cells. Cells were stably expressed with Bax and Bcl-xL with FRET pairs and real-time cell cycle indicator probes. Acceptor photobleaching and Fluorescence lifetime imaging revealed interaction dynamics between Bax and Bcl-xL in isogenic stable cells. While Bcl-xL inhibited cell cycle progression, Bax promoted the cell cycle. The study highlighted an increased Bax-Bcl-xL interaction in the G1 phase compared to the non-G1 phase. Increased interaction is seen under stressed conditions and Bax-activated cells with FLIM-FRET, highlighting the nature of Bax-Bcl-xL interaction during cellular stress. In conclusion, our study explains Bax-Bcl-xL interaction dynamics in real-time and the potential utility of the approach to study macromolecular interactions along with cell cycle and cell death.

利用flam - fret研究细胞周期和细胞死亡过程中Bax- Bcl-xL相互作用动力学。
群体中基因相同的细胞由于转录、表观遗传学、翻译后修饰以及随机或外部触发的非遗传改变的波动而表现出细胞间的可变性。蛋白质相互作用状态的变化也作为影响细胞周期和细胞死亡的额外细胞信号传导层出现。然而,在蛋白质-蛋白质相互作用时空变化的影响下,细胞周期进程与细胞死亡之间的相互关系很难在生长细胞中得到证实。这就需要在活细胞中对大分子相互作用进行细胞周期相分辨可视化的工具。我们描述了一种可视化的方法,在活细胞的细胞周期进程和细胞死亡过程中,亲和抗死亡信号伙伴Bax和Bcl-xL的相互作用。用FRET对和实时细胞周期指示探针稳定表达Bax和Bcl-xL细胞。受体光漂白和荧光寿命成像揭示了Bax和Bcl-xL在等基因稳定细胞中的相互作用动态。Bcl-xL抑制细胞周期进程,Bax促进细胞周期进程。该研究强调,与非G1期相比,G1期Bax-Bcl-xL相互作用增加。在应激条件下和bax激活的细胞与flm - fret的相互作用增加,突出了细胞应激期间Bax-Bcl-xL相互作用的性质。总之,我们的研究解释了Bax-Bcl-xL相互作用的实时动态,以及该方法在研究大分子相互作用与细胞周期和细胞死亡的潜在效用。
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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来源期刊
Cell Stress
Cell Stress Biochemistry, Genetics and Molecular Biology-Biochemistry, Genetics and Molecular Biology (miscellaneous)
CiteScore
13.50
自引率
0.00%
发文量
21
审稿时长
15 weeks
期刊介绍: Cell Stress is an open-access, peer-reviewed journal that is dedicated to publishing highly relevant research in the field of cellular pathology. The journal focuses on advancing our understanding of the molecular, mechanistic, phenotypic, and other critical aspects that underpin cellular dysfunction and disease. It specifically aims to foster cell biology research that is applicable to a range of significant human diseases, including neurodegenerative disorders, myopathies, mitochondriopathies, infectious diseases, cancer, and pathological aging. The scope of Cell Stress is broad, welcoming submissions that represent a spectrum of research from fundamental to translational and clinical studies. The journal is a valuable resource for scientists, educators, and policymakers worldwide, as well as for any individual with an interest in cellular pathology. It serves as a platform for the dissemination of research findings that are instrumental in the investigation, classification, diagnosis, and therapeutic management of major diseases. By being open-access, Cell Stress ensures that its content is freely available to a global audience, thereby promoting international scientific collaboration and accelerating the exchange of knowledge within the research community.
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