Maupin P, Pollard T D
J Cell Biol. 1983 Jan;96(1):51-62. doi: 10.1083/jcb.96.1.51.
Fixation of HeLa cells with a mixture of 100 mM glutaraldehyde, 2 mg/ml tannic acid and 0.5 mg/ml saponin allows the tannic acid to penetrate intact cells without disruption of membranes or extraction of the cytoplasmic matrix. After subsequent treatment with OsO4 cytoplasmic structures are stained so densely that fine details are visible even in very thin (dark gray) sections. Actin filaments are protected from disruption by OsO4 so that straight, densely stained filaments are seen in the cell cortex, filopodia, ruffling membranes, and stress fibers. Stress fibers also have 15-18-nm densities similar in appearance to myosin filaments. Tannic acid staining reveals that the coats of coated vesicles, pits, and plaques have a 12-nm layer of amorphous material between the membrane and the clathrin basketwork. HeLa cells have very large clathrin-coated membrane plaques on the basal surface. These coated membrane plaques appear to be a previously unrecognized site of cell-substrate adhesion.
用含有100 mM戊二醛、2 mg/ml单宁酸和0.5 mg/ml皂苷的混合物固定海拉细胞,可使单宁酸穿透完整细胞,而不破坏细胞膜或提取细胞质基质。在用四氧化锇进行后续处理后,细胞质结构被染得非常浓密,以至于即使在非常薄(深灰色)的切片中也能看到精细的细节。肌动蛋白丝受到保护,不被四氧化锇破坏,因此在细胞皮层、丝状伪足、褶皱膜和应力纤维中可以看到笔直的、染色浓密的丝。应力纤维还有15 - 18纳米的致密结构,外观与肌球蛋白丝相似。单宁酸染色显示,被膜小泡、小窝和斑块的被膜在膜和网格蛋白网络之间有一层12纳米厚的无定形物质。海拉细胞在基底表面有非常大的网格蛋白包被的膜斑块。这些包被的膜斑块似乎是一个以前未被认识的细胞与底物黏附的部位。