Albrecht-Buehler G
J Cell Biol. 1977 Mar;72(3):595-603. doi: 10.1083/jcb.72.3.595.
Using a new technique to visualize the tracks of moving 3T3 cells and combining it with the visualization of actin-containing microfilament bundles by indirect immunofluorescence (Lazarides, E. and K. Weber. 1974, Proc. Natl. Acad. Sci. U.S.A. 71:2268-2272), I present experiments which suggest that: (a) 30-40% of the pairs of daughter 3T3 mouse fibroblasts in noncloned cultures have mirror symmetrical actin-bundle patterns. (b) The angle between separating daughter cells is approx. 90 degrees or 180 degrees and seems related to the directions of certain actin-containing bundles. (c) Approximately 40% of separately moving daughter cells which did not collide with any other cell in the culture performed directional changes in a mirror symmetrical way. Both daughter cells entered the next mitosis at approximately the same time. I suggest that the actin-bundle pattern, the angle of separation, major directional changes during interphase, and the time of the next mitosis are predetermined by the parental cell.
利用一种可视化3T3细胞移动轨迹的新技术,并将其与通过间接免疫荧光观察含肌动蛋白的微丝束相结合(拉扎里德斯,E.和K.韦伯。1974年,《美国国家科学院院刊》71:2268 - 2272),我展示了一些实验,这些实验表明:(a)在未克隆培养的3T3小鼠成纤维细胞中,30 - 40%的子代细胞对具有镜像对称的肌动蛋白束模式。(b)分离的子代细胞之间的角度约为90度或180度,并且似乎与某些含肌动蛋白束的方向有关。(c)在培养物中未与任何其他细胞碰撞的单独移动的子代细胞中,约40%以镜像对称的方式进行方向改变。两个子代细胞几乎同时进入下一次有丝分裂。我认为肌动蛋白束模式、分离角度、间期的主要方向改变以及下一次有丝分裂的时间是由亲代细胞预先确定的。