Tago Tatsuya, Ogawa Takumi, Goto Yumi, Toyooka Kiminori, Tojima Takuro, Nakano Akihiko, Satoh Takunori, Satoh Akiko K
Program of Life and Environmental Science, Graduate School of Integral Science for Life, Hiroshima University, 1-7-1 Kagamiyama, Higashi-Hiroshima, Hiroshima, 739-8521, Japan.
Technology Platform Division, Mass Spectrometry and Microscopy Unit, RIKEN Center for Sustainable Resource Science, Yokohama, Kanagawa, 230-0045, Japan.
EMBO Rep. 2025 Feb;26(3):613-634. doi: 10.1038/s44319-024-00342-z. Epub 2024 Dec 10.
Live imaging of secretory cargoes is a powerful method for understanding the mechanisms of membrane trafficking. Inducing the synchronous release of cargoes from an organelle is key for enhancing microscopic observation. We developed an optical cargo-releasing method, 'retention using dark state of LOV2' (RudLOV), which enables precise spatial, temporal, and quantity control during cargo release. A limited amount of cargo-release using RudLOV is able to visualize cargo cisternal-movement and cargo-specific exit sites on the Golgi/trans-Golgi network. Moreover, by controlling the timing of cargo-release using RudLOV, we reveal the canonical and non-canonical effects of the well-known dynamin inhibitor dynasore, which inhibits early- but not late-Golgi transport and exits from the trans-Golgi network where dynamin-2 is active. Accumulation of COPI vesicles at the cis-side of the Golgi stacks in dynasore-treated cells suggests that dynasore targets COPI-uncoating/tethering/fusion machinery in the early-Golgi cisternae or endoplasmic reticulum but not in the late-Golgi cisternae. These results provide insight into the cisternal maturation of Golgi stacks.
对分泌性货物进行实时成像,是了解膜运输机制的一种强大方法。诱导细胞器中货物的同步释放,是增强显微镜观察效果的关键。我们开发了一种光学货物释放方法,即“利用LOV2的暗态进行保留”(RudLOV),该方法能够在货物释放过程中实现精确的空间、时间和数量控制。使用RudLOV进行有限量的货物释放,能够观察到货物在高尔基体/反式高尔基体网络上的囊泡移动和特定货物的出口位点。此外,通过使用RudLOV控制货物释放的时间,我们揭示了著名的发动蛋白抑制剂dynasore的经典和非经典作用,dynasore抑制早期高尔基体运输,但不抑制晚期高尔基体运输,也不抑制发动蛋白2活跃的反式高尔基体网络中的出口。在dynasore处理的细胞中,COPI囊泡在高尔基体堆叠的顺面积累,这表明dynasore作用于早期高尔基体囊泡或内质网中的COPI去包被/拴系/融合机制,而不是晚期高尔基体囊泡中的机制。这些结果为高尔基体堆叠的囊泡成熟提供了见解。