Aoki Kana, Maeda Fumiyo, Nagasako Tomoya, Mochizuki Yuki, Uchida Seiichi, Ikenouchi Junichi
Department of Biology, Faculty of Sciences, Kyushu University, Fukuoka 819-0395, Japan;
Department of Advanced Information Technology, Kyushu University, Fukuoka 819-0395, Japan;
Proc Natl Acad Sci U S A. 2016 Mar 29;113(13):E1863-71. doi: 10.1073/pnas.1600968113. Epub 2016 Mar 14.
The actin cytoskeleton usually lies beneath the plasma membrane. When the membrane-associated actin cytoskeleton is transiently disrupted or the intracellular pressure is increased, the plasma membrane detaches from the cortex and protrudes. Such protruded membrane regions are called blebs. However, the molecular mechanisms underlying membrane blebbing are poorly understood. This study revealed that epidermal growth factor receptor kinase substrate 8 (Eps8) and ezrin are important regulators of rapid actin reassembly for the initiation and retraction of protruded blebs. Live-cell imaging of membrane blebbing revealed that local reassembly of actin filaments occurred at Eps8- and activated ezrin-positive foci of membrane blebs. Furthermore, we found that a RhoA-ROCK-Rnd3 feedback loop determined the local reassembly sites of the actin cortex during membrane blebbing.
肌动蛋白细胞骨架通常位于质膜下方。当与膜相关的肌动蛋白细胞骨架暂时受到破坏或细胞内压力增加时,质膜会与皮质分离并突出。这种突出的膜区域称为泡状凸起。然而,膜泡状凸起背后的分子机制仍知之甚少。这项研究表明,表皮生长因子受体激酶底物8(Eps8)和埃兹蛋白是快速肌动蛋白重新组装以启动和缩回突出的泡状凸起的重要调节因子。膜泡状凸起的活细胞成像显示,肌动蛋白丝的局部重新组装发生在膜泡状凸起的Eps8和活化的埃兹蛋白阳性位点。此外,我们发现RhoA-ROCK-Rnd3反馈环决定了膜泡状凸起过程中肌动蛋白皮质的局部重新组装位点。