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Requirement of Gab2 for mast cell development and KitL/c-Kit signaling
Authors:Nishida Keigo  Wang Lin  Morii Eiichi  Park Sung Joo  Narimatsu Masahiro  Itoh Shousaku  Yamasaki Satoru  Fujishima Masahiro  Ishihara Katsuhiko  Hibi Masahiko  Kitamura Yukihiko  Hirano Toshio
Affiliation:Department of Molecular Oncology (C-7), Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Abstract:
Mast cells are thought to participate in a variety of immune responses, such as parasite resistance and the allergic reaction. Mast cell development depends on stem cell factor (Kit ligand) and its receptor, c-Kit. Gab2 is an adaptor molecule containing a pleckstrin homology domain and potential binding sites for SH2 and SH3 domains. Gab2 is phosphorylated on tyrosine after stimulation with cytokines and growth factors, including KitL. Gab2-deficient mice were created to define the physiological requirement for Gab2 in KitL/c-Kit signaling and mast cell development. In Gab2-deficient mice, the number of mast cells was reduced markedly in the stomach and less severely in the skin. Bone marrow-derived mast cells (BMMCs) from the Gab2-deficient mice grew poorly in response to KitL. KitL-induced ERK MAP kinase and Akt activation were impaired in Gab2-deficient BMMCs. These data indicate that Gab2 is required for mast cell development and KitL/c-Kit signaling.
Keywords:
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