Nishio K, Inoue A, Qiao S, Kondo H, Mimura A
Department of Anatomy and Cell Biology, Nagoya University School of Medicine, 65 Tsurumai-Cho, Showa-Ku, Nagoya 466-8550, Japan.
Histochem Cell Biol. 2001 Oct;116(4):321-7. doi: 10.1007/s004180100325.
One characteristic feature of senescent fibroblasts is flat, enlarged, and heterogeneous cell shapes. The present study was aimed to understand the structural basis of the senescent cell morphology. SDS-gel electrophoresis as well as western blotting demonstrated that there occurred a prominent protein band about 57 kDa in the senescent cells as compared with normal young or immortalized cells growing rapidly, and the protein was identified with a cytoskeletal protein, vimentin. In fact, senescent fibroblasts contained approximately threefold more vimentin protein, and fourfold more vimentin mRNA than young embryonic fibroblasts. In the senescent cells, vimentin cytoskeleton occurred as densely bundled filaments in parallel with the long axis of cell bodies, whereas in young or actively growing cells it showed short and thin vimentin filaments or fur-like irregular networks. It was further demonstrated that senescent cell shapes could be induced when a vimentin expression construct was transfected in young fibroblasts. These results suggest that senescent fibroblasts overproduce vimentin protein, and the overproduced vimentin filaments bring about the senescent cell morphology.
衰老成纤维细胞的一个特征是细胞形态扁平、增大且不均一。本研究旨在了解衰老细胞形态的结构基础。SDS凝胶电泳以及蛋白质印迹法表明,与快速生长的正常年轻细胞或永生化细胞相比,衰老细胞中出现了一条约57 kDa的明显蛋白条带,该蛋白被鉴定为一种细胞骨架蛋白,波形蛋白。事实上,衰老成纤维细胞中波形蛋白的含量大约是年轻胚胎成纤维细胞的三倍,波形蛋白mRNA的含量则是其四倍。在衰老细胞中,波形蛋白细胞骨架呈现为与细胞体的长轴平行的密集束状细丝,而在年轻或活跃生长的细胞中,它表现为短而细的波形蛋白细丝或毛状不规则网络。进一步证明,当在年轻成纤维细胞中转染波形蛋白表达构建体时,可以诱导出衰老细胞的形态。这些结果表明,衰老成纤维细胞过度产生波形蛋白,而过度产生的波形蛋白细丝导致了衰老细胞的形态。