Wang E, Gundersen D
Exp Cell Res. 1984 Sep;154(1):191-202. doi: 10.1016/0014-4827(84)90679-7.
Fibroblastic cells of human origin have a limited lifespan in culture. One of the senescence-associated phenotypic changes is an increase in the abundance of cytoplasmic filaments. Human skin fibroblasts (strain 0011), derived from an 8-week-old male fetus, were passaged according to a predetermined schedule and examined at successive population doubling levels. In young rapidly growing cultures, fluorescence microscopy with NBD-Phallacidin shows a normal organization of the actin-containing fibers, microtubules and intermediate filaments, as has been described previously. At stages close to the end of the in vitro lifespan of the cell strain, large flat fibroblasts are the predominant cell type in culture. These large senescent fibroblasts contain numerous prominent actin fibers traversing the entire long axis of the cytoplasm. The fibers are often located adjacent to each other and appear to form a sheet on the ventral side of the cytoplasm. Staining of senescent cells with anti-tubulin antibody reveals an increase in the abundance of microtubules per cell and the distribution pattern is altered through the increase in the number of organization centers. Intermediate filaments are also more abundant and display tightly packed fibrillar sheets or bundles. Electron microscopic studies have confirmed the increased organization of microfilaments into bundles in senescent cells. These results suggest that during in vitro senescence, the increase in cell size is correlated with increased organization of the cytoskeleton. The presence of a rigid cytoskeletal structure may contribute in part to the inability of the senescent cell to replicate.
源自人类的成纤维细胞在培养中的寿命有限。与衰老相关的表型变化之一是细胞质细丝丰度的增加。从一名8周大男性胎儿获取的人皮肤成纤维细胞(0011株)按照预定时间表传代,并在连续的群体倍增水平下进行检测。在年轻且快速生长的培养物中,用NBD - 鬼笔环肽进行荧光显微镜观察显示,含肌动蛋白的纤维、微管和中间丝的组织正常,如先前所述。在接近细胞株体外寿命结束的阶段,大的扁平成纤维细胞是培养物中的主要细胞类型。这些大的衰老成纤维细胞含有许多突出的肌动蛋白纤维,横穿细胞质的整个长轴。这些纤维常常彼此相邻定位,并且似乎在细胞质腹侧形成一片。用抗微管蛋白抗体对衰老细胞进行染色显示,每个细胞的微管丰度增加,并且通过组织中心数量的增加,分布模式发生改变。中间丝也更加丰富,并呈现紧密堆积的纤维状片层或束状。电子显微镜研究证实了衰老细胞中微丝束状组织的增加。这些结果表明,在体外衰老过程中,细胞大小的增加与细胞骨架组织的增加相关。刚性细胞骨架结构的存在可能部分导致衰老细胞无法复制。