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Insulin-Induced Circular Membrane Ruffling on Rat 1 Cells Expressing a High Number of Human Insulin Receptors: Circular Ruffles Caused by Rapid Actin Reorganization Exhibit High Density of Insulin Receptors and Phosphotyrosines
Authors:Shu-lian Li  Yoshihiko Miyata  Ichiro Yahara  Yoko Fujita-Yamaguchi
Institution:1. Basic and Clinical Myology Laboratory, Department of Physiology, University of Melbourne, VIC 3010, Australia;2. Institute for Genome Biology, Leibniz Institute for Farm Animal Biology (FBN), 18196, Dummerstorf, Germany;3. Muscle Biology and Therapeutics Laboratory, Baker IDI Heart and Diabetes Institute, Melbourne, VIC 3004, Australia;4. F. Hoffmann-La Roche Ltd., pRED, Pharma Research & Early Development, DTA Neuroscience, 4070, Basel, Switzerland;1. Graduated Institute of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan;2. School of Dentistry, Kaohsiung Medical University, Kaohsiung, Taiwan;3. Department of Biological Sciences, National Sun Yat-sen University, Kaohsiung, Taiwan;4. Faculty of Science and Engineering, Tokushima Bunri University, Sanuki, Japan;5. Department of Molecular Preventive Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan
Abstract:The early effects of insulin on morphological changes were examined using Rat 1 cells expressing one million human insulin receptors (Rat1HIR cells). Insulin transiently induced circular membrane ruffling on Rat1HIR cells. The circular ruffles were detected by phase microscopy as well as by fluorescence microscopy when actin was stained with rhodamine-conjugated phalloidin. The circular ruffles were also visualized by fluorescence microscopy when stained with either antiinsulin receptor monoclonal antibody, αIR-1, or antiphosphotyrosine antibody, followed by fluorescein isothiocyanate-labeled second antibodies. Control Rat1 cells or Rat1HIR A/K1018 cells expressing kinase-defective insulin receptors did not show any circular ruffles when treated with insulin. These results suggest that the circular ruffles are formed by actin reorganization induced by insulin and that this process requires the protein-tyrosine kinase activity of the receptor. Detection of insulin receptors and phosphotyrosines in the circular ruffles suggests the possibility that the insulin receptors in the ruffles may be highly active and phosphorylating either the receptors themselves or proteins associated with the ruffles. These results are consistent with our previous in vitro observations that a large aggregate form of the purified insulin receptor is a highly active protein-tyrosine kinase.
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