Numata O, Yasuda T, Watanabe Y
Institute of Biological Sciences, University of Tsukuba, Ibaraki, Japan.
Exp Cell Res. 1995 May;218(1):123-31. doi: 10.1006/excr.1995.1138.
Tetrahymena 14-nm filament protein has been shown to have dual functions as a citrate synthase in mitochondria and as a cytoskeletal protein in oral morphogenesis and pronuclear behavior during conjugation. Immunofluorescence studies of the 14-nm filament protein/citrate synthase in mitochondria found that intense mitochondrial fluorescence remained unchanged in Tetrahymena cells taken from logarithmic growth phase to stationary phase. However, electron microscopic studies showed that electron-dense rod-shaped structures found in mitochondrial matrices tended to increase in Tetrahymena cells in the growth decline phase. The rods were composed of side-by-side straight filaments with diameters of approximately 14 to 16 nm. Serial sections revealed that in Tetrahymena cells in growth decline phase, one to four electron-dense rods existed in the matrices of every mitochondrion. Immunoelectron microscopy using an anti-14-nm filament antibody clearly showed that a filament bundle of the electron-dense rod was the bundle of polymerized filaments of 14-nm filament protein/citrate synthase. These results strongly suggest that dynamic monomer-polymer conversion of the 14-nm filament protein/citrate synthase in mitochondria depends upon the physiological conditions of Tetrahymena cells.
嗜热四膜虫14纳米丝蛋白已被证明具有双重功能,它在线粒体中作为柠檬酸合酶,在接合过程中的口器形态发生和原核行为中作为细胞骨架蛋白。对线粒体中14纳米丝蛋白/柠檬酸合酶的免疫荧光研究发现,从对数生长期到稳定期的嗜热四膜虫细胞中,强烈的线粒体荧光保持不变。然而,电子显微镜研究表明,在生长衰退期的嗜热四膜虫细胞中,线粒体基质中发现的电子致密杆状结构有增加的趋势。这些杆由直径约为14至16纳米的并排直丝组成。连续切片显示,在生长衰退期的嗜热四膜虫细胞中,每个线粒体基质中有一到四根电子致密杆。使用抗14纳米丝抗体的免疫电子显微镜清楚地表明,电子致密杆的丝束是14纳米丝蛋白/柠檬酸合酶的聚合丝束。这些结果强烈表明,线粒体中14纳米丝蛋白/柠檬酸合酶的动态单体-聚合物转化取决于嗜热四膜虫细胞的生理条件。