Boucrot Emmanuel, Kirchhausen Tomas
Department of Cell Biology and CBR Institute for Biomedical Research, Harvard Medical School, 200 Longwood Avenue, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2007 May 8;104(19):7939-44. doi: 10.1073/pnas.0702511104. Epub 2007 May 1.
The shape and total surface of a cell and its daughters change during mitosis. Many cells round up during prophase and metaphase and reacquire their extended and flattened shape during cytokinesis. How does the total area of plasma membrane change to accommodate these morphological changes and by what mechanism is control of total membrane area achieved? Using single-cell imaging methods, we have found that the amount of plasma membrane in attached cells in culture decreases at the beginning of mitosis and recovers rapidly by the end. Clathrin-based endocytosis is normal throughout all phases of cell division, whereas recycling of internalized membranes back to the cell surface slows considerably during the rounding up period and resumes at the time at which recovery of cell membrane begins. Interference with either one of these processes by genetic or chemical means impairs cell division. The total cell-membrane area recovers even in the absence of a functional Golgi apparatus, which would be needed for export of newly synthesized membrane lipids and proteins. We propose a mechanism by which modulation of endosomal recycling controls cell area and surface expression of membrane-bound proteins during cell division.
细胞及其子代细胞在有丝分裂过程中,其形状和总表面积会发生变化。许多细胞在前期和中期会变圆,并在胞质分裂期间恢复其伸长和平坦的形状。质膜的总面积是如何变化以适应这些形态变化的,以及通过何种机制实现对总膜面积的控制?使用单细胞成像方法,我们发现培养中贴壁细胞的质膜量在有丝分裂开始时减少,并在末期迅速恢复。基于网格蛋白的内吞作用在细胞分裂的所有阶段都是正常的,而内化膜回到细胞表面的再循环在变圆期显著减慢,并在细胞膜开始恢复时恢复。通过遗传或化学手段干扰这些过程中的任何一个都会损害细胞分裂。即使在没有功能性高尔基体的情况下,总细胞膜面积也会恢复,而高尔基体是新合成的膜脂和蛋白质输出所必需的。我们提出了一种机制,通过这种机制,内体再循环的调节在细胞分裂过程中控制细胞面积和膜结合蛋白的表面表达。