Subcortical fibrils composed of bundles of F-actin filaments and endoplasmic filaments are responsible for endoplasmic streaming. It is reported here that these fibrils and filaments move actively in an artificial medium containing Mg-ATP and sucrose at neutral pH, when the medium was added to the cytoplasm squeezed out of the cell. The movement was observed by phase-contrast microscopy or dark-field microscopy and recorded on 16-mm film. Chains of chloroplasts linked by subcortical fibrils showed translational movement in the medium. Even after all chloroplasts and the endoplasm were washed away by perfusion with fresh medium, free fibrils and/or filaments (henceforth, referred to as fibers) not attached to chloroplasts continued travelling in the direction of the fiber orientation. Sometimes the fibers formed rings and rotated. Chloroplast chains and free fibers or rings continued moving for 5-30 min at about half the rate of the endoplasmic streaming in vivo. Calcium ion concentrations < 10(-7) M permitted movement to take place. Electron microscopy revealed that both fibers and rings were bundles of F-actin filaments that showed the same polarity after decoration with heavy meromyosin.
Article| December 01 1980
Active movement in vitro of bundle of microfilaments isolated from Nitella cell.
Online Issn: 1540-8140
Print Issn: 0021-9525
J Cell Biol (1980) 87 (3): 569–578.
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S Higashi-Fujime; Active movement in vitro of bundle of microfilaments isolated from Nitella cell.. J Cell Biol 1 December 1980; 87 (3): 569–578. doi: https://doi.org/10.1083/jcb.87.3.569
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