The tetraspanin CD9 modulates epidermal growth factor receptor signaling in cancer cells

• Published in: Journal of cellular physiology Vol. 216; no. 1; pp. 135 - 143
• Main Authors: Murayama, Yoko, Shinomura, Yasuhisa, Oritani, Kenji, Miyagawa, Jun-Ichiro, Yoshida, Hitoshi, Nishida, Makoto, Katsube, Fumie, Shiraga, Masamichi, Miyazaki, Tamana, Nakamoto, Taisei, Tsutsui, Shusaku, Tamura, Shinji, Higashiyama, Shigeki, Shimomura, Iichirou, Hayashi, Norio
• Format: Journal Article
• Language: English
• Published: Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.07.2008
• Subjects: Animals; Antibodies - metabolism; Antigens, CD - genetics; Antigens, CD - metabolism; Cell Line, Tumor - metabolism; Cricetinae; Humans; Integrin beta1 - metabolism; Membrane Glycoproteins - genetics; Membrane Glycoproteins - metabolism; Multiprotein Complexes - metabolism; Neoplasms - metabolism; Neoplasms - pathology; Receptor, Epidermal Growth Factor - genetics; Receptor, Epidermal Growth Factor - metabolism; RNA, Small Interfering - genetics; RNA, Small Interfering - metabolism; Signal Transduction - physiology; Tetraspanin-29
• ISSN: 0021-9541; 1097-4652
• DOI: 10.1002/jcp.21384

CD9 is a member of the tetraspanins, and has been shown to be involved in a variety of cellular activities such as migration, proliferation, and adhesion. In addition, it has been known that CD9 can associate with other proteins. Here we demonstrated the physical and functional association of CD9 with epidermal growth factor receptor (EGFR) on MKN‐28 cells. Double‐immunofluorescent staining and immunoprecipitation demonstrated the complex formation of CD9‐EGFR and CD9‐β1 integrin, and that both complexes are colocalized on the cell surface especially at the cell–cell contact site. Anti‐CD9 monoclonal antibody ALB6 induced a dotted or patch‐like aggregation pattern of both CD9‐EGFR and CD9‐β1 integrin. The internalization of EGFR after EGF‐stimulation was significantly enhanced by the treatment with ALB6. CD9 can associate with EGFR in hepatocellular carcinoma cells (HepG2/CD9) and Chinese hamster ovary cancer cells (CHO‐HER/CD9), which were transfected with pTJ/human EGFR/CD9. Furthermore expression of CD9 specifically attenuated EGFR signaling in CHO‐HER/CD9 cells through the down regulation of surface expression of EGFR. These results suggest that CD9 might have an important role that attenuates EGFR signaling. Therefore, CD9 not only associates EGFR but also a new regulator, which may affect EGF‐induced signaling in cancer cells. J. Cell. Physiol. 216: 135–143, 2008. © 2008 Wiley‐Liss, Inc.