| Literature DB >> 11861309 |
Keigo Nishida1, Lin Wang, Eiichi Morii, Sung Joo Park, Masahiro Narimatsu, Shousaku Itoh, Satoru Yamasaki, Masahiro Fujishima, Katsuhiko Ishihara, Masahiko Hibi, Yukihiko Kitamura, Toshio Hirano.
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.Entities:
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Year: 2002 PMID: 11861309 DOI: 10.1182/blood.v99.5.1866
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113