移动和静止的肌动蛋白丝参与有丝分裂后PtK2细胞的铺展。
Moving and stationary actin filaments are involved in spreading of postmitotic PtK2 cells.
作者信息
Cramer L, Mitchison T J
机构信息
Department of Pharmacology, University of California, San Francisco 94143-0450.
出版信息
J Cell Biol. 1993 Aug;122(4):833-43. doi: 10.1083/jcb.122.4.833.
We have investigated spreading of postmitotic PtK2 cells and the behavior of actin filaments in this system by time-lapse microscopy and photoactivation of fluorescence. During mitosis PtK2 cells round up and at cytokinesis the daughter cells spread back to regain their interphase morphology. Normal spreading edges are quite homogenous and are not comprised of two distinct areas (lamellae and lamellipodia) as found in moving edges of interphase motile cells. Spreading edges are connected to a network of long, thin, actin-rich fibers called retraction fibers. A role for retraction fibers in spreading was tested by mechanical disruption of fibers ahead of a spreading edge. Spreading is inhibited over the region of disruption, but not over neighboring intact fibers. Using photoactivation of fluorescence to mark actin filaments, we have determined that the majority of actin filaments move forward in spreading edges at the same rate as the edge. As far as we are aware, this is the first time that forward movement of a cell edge has been correlated with forward movement of actin filaments. In contrast, actin filaments in retraction fibers remain stationary with respect to the substrate. Thus there are at least two dynamic populations of actin polymer in spreading postmitotic cells. This is supported by the observation that actin filaments in some spreading edges not only move forward, but also separate into two fractions or broaden with time. A small fraction of postmitotic cells have a spreading edge with a distinct lamellipodium. In these edges, marked actin polymer fluxes backward with respect to substrate. We suggest that forward movement of actin filaments may participate in generating force for spreading in postmitotic cells and perhaps more generally for cell locomotion.
我们通过延时显微镜和荧光光激活技术,研究了有丝分裂后PtK2细胞的铺展以及该系统中肌动蛋白丝的行为。在有丝分裂期间,PtK2细胞变圆,在胞质分裂时,子细胞铺展回原来的形态,重新获得间期形态。正常的铺展边缘相当均匀,不像间期运动细胞的移动边缘那样由两个不同的区域(片状伪足和丝状伪足)组成。铺展边缘与一个由长而细、富含肌动蛋白的纤维组成的网络相连,这些纤维称为收缩纤维。我们通过机械破坏铺展边缘前方的纤维,来测试收缩纤维在铺展过程中的作用。在破坏区域上方铺展受到抑制,但在相邻的完整纤维上不受影响。利用荧光光激活技术标记肌动蛋白丝,我们确定,大多数肌动蛋白丝在铺展边缘以与边缘相同的速度向前移动。据我们所知,这是首次将细胞边缘的向前移动与肌动蛋白丝的向前移动联系起来。相比之下,收缩纤维中的肌动蛋白丝相对于底物保持静止。因此,在有丝分裂后铺展的细胞中,至少有两种动态的肌动蛋白聚合物群体。这一观点得到了以下观察结果的支持:在一些铺展边缘,肌动蛋白丝不仅向前移动,而且随着时间的推移会分成两部分或变宽。一小部分有丝分裂后细胞的铺展边缘有明显的丝状伪足。在这些边缘,标记的肌动蛋白聚合物相对于底物向后流动。我们认为,肌动蛋白丝的向前移动可能参与为有丝分裂后细胞的铺展产生力,或许更普遍地参与细胞运动。