Barazzuol Lucia, Tykhonenko Tetiana, Griffiths Tia L, Vagnoni Alessio, Brini Marisa, Calì Tito
Department of Biomedical Sciences (DSB), University of Padova, Padova, Italy.
Department of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.
Cell Death Dis. 2025 Mar 27;16(1):214. doi: 10.1038/s41419-025-07511-5.
Organelle contact sites are crucial for cellular function, enabling the exchange of lipids, ions, and other molecules between different organelles. The ability to track these contact sites in vivo has been significantly advanced by the development of SPLICS (Split-GFP-based Contact Site Sensors) reporters, which have provided unprecedented insights into the intricate network of organelle communication. This innovative and powerful tool allows the real-time visualization of different organelle interactions in living cells and in vivo thus unraveling the complexity of their dynamic in the context of cellular homeostasis. Recent studies highlighted the dynamic nature of organelle contact sites either in terms of tethering/untethering and of movement of the contact itself in time and space: whether unique temporal behaviors and contact site-specific dynamics of different organelle interactions exist is currently unknown. In this study, we investigated the spatiotemporal distribution of various organelle contact sites using time-lapse in vitro and in vivo imaging and discovered an evolutionarily conserved dynamic pattern among different contact sites, influenced by the specific partner organelles involved. These findings highlight the importance of spatial and temporal regulation at organelle contact sites, which may underlie their diverse physiological functions. The discovery of contact site-specific dynamics opens new avenues for understanding the regulation of organelle interactions in health and disease, with potential implications for developing targeted therapeutic strategies.
细胞器接触位点对于细胞功能至关重要,它能够使不同细胞器之间进行脂质、离子及其他分子的交换。基于分裂绿色荧光蛋白的接触位点传感器(SPLICS)报告基因的开发显著推动了在体内追踪这些接触位点的能力,该报告基因使人们对细胞器通讯的复杂网络有了前所未有的深入了解。这个创新且强大的工具能够实时可视化活细胞和体内不同细胞器之间的相互作用,从而揭示它们在细胞稳态背景下动态变化的复杂性。最近的研究强调了细胞器接触位点在系留/解系留以及接触位点本身在时间和空间上移动方面的动态性质:目前尚不清楚不同细胞器相互作用是否存在独特的时间行为和接触位点特异性动态变化。在本研究中,我们使用体外和体内延时成像研究了各种细胞器接触位点的时空分布,发现不同接触位点之间存在一种受特定伙伴细胞器影响的进化保守动态模式。这些发现突出了细胞器接触位点时空调节的重要性,这可能是其多样生理功能的基础。接触位点特异性动态变化的发现为理解健康和疾病状态下细胞器相互作用的调节开辟了新途径,对开发靶向治疗策略具有潜在意义。