Halikar Aman M, Chandrasekharan Aneesh, Lekshmi Asha, Sivasailam Aswathy, Tiffee P J Jain, Tiwari Shivanshu K, Rather Aijaz Ahmad, Santhoshkumar T R
Cancer Research Program, Rajiv Gandhi Centre for Biotechnology, Poojappura, Thycaud P.O., Thiruvananthapuram, Kerala 695014, India.
Manipal Academy of Higher Education (MAHE), Manipal, Karnataka-576104, India.
Cell Stress. 2025 Jul 8;9:143-157. doi: 10.15698/cst2025.07.307. eCollection 2025.
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.
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在触发的非遗传改变的波动而表现出细胞间的变异性。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细胞信号传导的额外层面出现。然而,在生长的细胞中,很难证明蛋白质-蛋白质相互作用的时空变化影响下细胞周期进程与细胞死亡之间的相互关系。这需要用于活细胞中大分子相互作用的细胞周期阶段分辨可视化的工具。我们描述了一种在活细胞的细胞周期进程和细胞死亡过程中可视化促死亡和抗死亡信号伴侣Bax和Bcl-xL相互作用的方法。用带有FRET对和实时细胞周期指示剂探针的Bax和Bcl-xL稳定表达细胞。受体光漂白和荧光寿命成像揭示了同基因稳定细胞中Bax和Bcl-xL之间的相互作用动力学。虽然Bcl-xL抑制细胞周期进程,但Bax促进细胞周期。该研究强调与非G1期相比,G1期Bax-Bcl-xL相互作用增加。在应激条件下以及用FLIM-FRET检测的Bax激活细胞中可见相互作用增加,突出了细胞应激期间Bax-Bcl-xL相互作用的性质。总之,我们的研究实时解释了Bax-Bcl-xL相互作用动力学以及该方法在研究大分子相互作用以及细胞周期和细胞死亡方面的潜在用途。