Laboratory of Molecular Biology and Cell Informatics, Graduate School of Life and Environmental Sciences, Osaka Prefecture University Live Cell Imaging Institute, Osaka Prefecture University
Kaori SENDA-MURATA
Laboratory of Molecular Biology and Cell Informatics, Graduate School of Life and Environmental Sciences, Osaka Prefecture University Live Cell Imaging Institute, Osaka Prefecture University
Shigenori OKA
Laboratory of Molecular Biology and Cell Informatics, Graduate School of Life and Environmental Sciences, Osaka Prefecture University The Second Laboratories, Research and Development Center, Nagase & Co., Ltd. Live Cell Imaging Institute, Osaka Prefecture University
Kenji SUGIMOTO
Laboratory of Molecular Biology and Cell Informatics, Graduate School of Life and Environmental Sciences, Osaka Prefecture University Live Cell Imaging Institute, Osaka Prefecture University
To analyze aberrant spindle formation by microtubule-targeting drugs, live cell imaging was performed using multi-fluorescent human MDA-MB-435 cells in which several spindle components were visualized. Time-lapse images revealed that nocodazole and vinblastine induced additional perinuclear asters at the onset of mitosis. These results imply that these drugs stimulate the microtubule-organizing activity, despite their microtubule-destabilizing properties.
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