Hynes R O, Destree A T
Cell. 1978 Jan;13(1):151-63. doi: 10.1016/0092-8674(78)90146-0.
An antibody was raised against an electrophoretically homogeneous protein from cultured fibroblasts and shown to be directed against 10 nm filaments. The antiserum did not stain microtubules or actin microfilaments. The distribution of 10 nm filaments in normal cells was studied during growth, spreading, locomotion, mitosis, and after treatment with colchicine and cytochalasin B. The 58,000 dalton subunit protein is apparently all polymerized in the filaments which are insoluble in nonionic detergent. The distribution of 10 nm filaments is altered by colchicine treatments which disrupt microtubules. The organization of 10 nm filaments is altered in transformed cells.
制备了一种针对培养成纤维细胞中电泳纯一蛋白质的抗体,结果表明该抗体针对的是10纳米细丝。抗血清不使微管或肌动蛋白微丝染色。研究了正常细胞在生长、铺展、移动、有丝分裂过程中以及在用秋水仙碱和细胞松弛素B处理后10纳米细丝的分布情况。58,000道尔顿的亚基蛋白显然全部聚合在不溶于非离子去污剂的细丝中。秋水仙碱处理破坏微管后,10纳米细丝的分布会发生改变。在转化细胞中,10纳米细丝的组织会发生改变。