Osborn M, Franke W W, Weber K
Proc Natl Acad Sci U S A. 1977 Jun;74(6):2490-4. doi: 10.1073/pnas.74.6.2490.
During our studies with antibodies against structural proteins of the cytoskeleton of eukaryotic cells we have observed that sera from many normal rabbits decorate a fiber system in cells of the established rat kangaroo cell line Pt K2. The display and organization of these fibers are different from those of microfilament bundles (decorated by antibody to actin) and microtubules (decorated by antibody to tubulin). This new fiber system can be further distinguished by its resistance to reorganization when cells are treated with Colcemid or cytochalasin B. The decoration of this fiber system is not detected if Pt K2 cells are fixed with formaldehyde. Such sera also appear to decorate swirls of perinuclear fibers in mouse Neuro 2a cells, and in mouse 3T3 cells treated with mitotic drugs. Comparison of the immunofluorescence pictures with electron microscopic data suggests that the sera are visualizing bundles of intermediate 7- to 10-nm filaments.
在我们利用针对真核细胞细胞骨架结构蛋白的抗体进行研究的过程中,我们观察到,许多正常兔的血清能够使已建立的大鼠袋鼠细胞系Pt K2的细胞中的一种纤维系统显色。这些纤维的呈现方式和组织形式不同于微丝束(由抗肌动蛋白抗体显色)和微管(由抗微管蛋白抗体显色)。当用秋水仙酰胺或细胞松弛素B处理细胞时,这种新的纤维系统因其对重组的抗性而能够进一步被区分出来。如果用甲醛固定Pt K2细胞,则检测不到这种纤维系统的显色情况。此类血清似乎也能使小鼠Neuro 2a细胞以及用有丝分裂药物处理过的小鼠3T3细胞中的核周纤维漩涡显色。将免疫荧光图片与电子显微镜数据进行比较表明,这些血清所显示的是7至10纳米的中间丝束。