FBP17-mediated finger-like membrane protrusions in cell competition between normal and RasV12-transformed cells
Tomoko Kamasaki,
Yumi Miyazaki,
Susumu Ishikawa,
Kazuya Hoshiba,
Keisuke Kuromiya,
Nobuyuki Tanimura,
Yusuke Mori,
Motosuke Tsutsumi,
Tomomi Nemoto,
Ryota Uehara,
Shiro Suetsugu,
Toshiki Itoh,
Yasuyuki Fujita
Affiliations
Tomoko Kamasaki
Division of Molecular Oncology, Institute for Genetic Medicine, Hokkaido University Graduate School of Chemical Sciences and Engineering, Sapporo, Hokkaido 060-0815, Japan; Faculty of Advanced Life Science, Hokkaido University, Sapporo, Hokkaido 001-0021, Japan; Corresponding author
Yumi Miyazaki
Division of Molecular Oncology, Institute for Genetic Medicine, Hokkaido University Graduate School of Chemical Sciences and Engineering, Sapporo, Hokkaido 060-0815, Japan
Susumu Ishikawa
Division of Molecular Oncology, Institute for Genetic Medicine, Hokkaido University Graduate School of Chemical Sciences and Engineering, Sapporo, Hokkaido 060-0815, Japan
Kazuya Hoshiba
Division of Molecular Oncology, Institute for Genetic Medicine, Hokkaido University Graduate School of Chemical Sciences and Engineering, Sapporo, Hokkaido 060-0815, Japan
Keisuke Kuromiya
Division of Molecular Oncology, Institute for Genetic Medicine, Hokkaido University Graduate School of Chemical Sciences and Engineering, Sapporo, Hokkaido 060-0815, Japan; Department of Molecular Oncology, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan
Nobuyuki Tanimura
Division of Molecular Oncology, Institute for Genetic Medicine, Hokkaido University Graduate School of Chemical Sciences and Engineering, Sapporo, Hokkaido 060-0815, Japan; Department of Molecular Oncology, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan
Yusuke Mori
Division of Molecular Oncology, Institute for Genetic Medicine, Hokkaido University Graduate School of Chemical Sciences and Engineering, Sapporo, Hokkaido 060-0815, Japan; Department of Molecular Oncology, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan
Motosuke Tsutsumi
Research Institute for Electronic Science, Hokkaido University, Sapporo, Hokkaido 001-0020, Japan; Exploratory Research Center on Life and Living Systems (ExCELLS) & National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Aichi 444-8787, Japan
Tomomi Nemoto
Research Institute for Electronic Science, Hokkaido University, Sapporo, Hokkaido 001-0020, Japan; Exploratory Research Center on Life and Living Systems (ExCELLS) & National Institute for Physiological Sciences, National Institutes of Natural Sciences, Okazaki, Aichi 444-8787, Japan
Ryota Uehara
Faculty of Advanced Life Science, Hokkaido University, Sapporo, Hokkaido 001-0021, Japan
Shiro Suetsugu
Division of Biological Science, Nara Institute of Science and Technology, Ikoma, Nara 630-0192, Japan
Toshiki Itoh
Division of Membrane Biology, Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, Kobe, Hyogo 650-0017, Japan; Biosignal Research Center, Kobe University, Kobe, Hyogo 657-8501, Japan
Yasuyuki Fujita
Division of Molecular Oncology, Institute for Genetic Medicine, Hokkaido University Graduate School of Chemical Sciences and Engineering, Sapporo, Hokkaido 060-0815, Japan; Department of Molecular Oncology, Graduate School of Medicine, Kyoto University, Kyoto 606-8501, Japan; Corresponding author
Summary: At the initial stage of carcinogenesis, cell competition often occurs between newly emerging transformed cells and the neighboring normal cells, leading to the elimination of transformed cells from the epithelial layer. For instance, when RasV12-transformed cells are surrounded by normal cells, RasV12 cells are apically extruded from the epithelium. However, the underlying mechanisms of this tumor-suppressive process still remain enigmatic. We first show by electron microscopic analysis that characteristic finger-like membrane protrusions are projected from both normal and RasV12 cells at their interface. In addition, FBP17, a member of the F-BAR proteins, accumulates in RasV12 cells, as well as surrounding normal cells, which plays a positive role in the formation of finger-like protrusions and apical elimination of RasV12 cells. Furthermore, cdc42 acts upstream of these processes. These results suggest that the cdc42/FBP17 pathway is a crucial trigger of cell competition, inducing “protrusion to protrusion response” between normal and RasV12-transformed cells.