Requirement of Gab2 for mast cell development and KitL/c-Kit signaling |
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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 |
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Affiliation: | Department of Molecular Oncology (C-7), Osaka University Graduate School of Medicine, Suita, Osaka, Japan. |
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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. |
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