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Cell surface localization of importin α1/KPNA2 affects cancer cell proliferation by regulating FGF1 signalling

Importin α1 is involved in nuclear import as a receptor for proteins with a classical nuclear localization signal (cNLS). Here, we report that importin α1 is localized to the cell surface in several cancer cell lines and detected in their cultured medium. We also found that exogenously added importi...

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Detalles Bibliográficos
Autores principales: Yamada, Kohji, Miyamoto, Yoichi, Tsujii, Akira, Moriyama, Tetsuji, Ikuno, Yudai, Shiromizu, Takashi, Serada, Satoshi, Fujimoto, Minoru, Tomonaga, Takeshi, Naka, Tetsuji, Yoneda, Yoshihiro, Oka, Masahiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4757827/
https://www.ncbi.nlm.nih.gov/pubmed/26887791
http://dx.doi.org/10.1038/srep21410
Descripción
Sumario:Importin α1 is involved in nuclear import as a receptor for proteins with a classical nuclear localization signal (cNLS). Here, we report that importin α1 is localized to the cell surface in several cancer cell lines and detected in their cultured medium. We also found that exogenously added importin α1 is associated with the cell membrane via interaction with heparan sulfate. Furthermore, we revealed that the cell surface importin α1 recognizes cNLS-containing substrates. More particularly, importin α1 bound directly to FGF1 and FGF2, secreted cNLS-containing growth factors, and addition of exogenous importin α1 enhanced the activation of ERK1/2, downstream targets of FGF1 signalling, in FGF1-stimulated cancer cells. Additionally, anti-importin α1 antibody treatment suppressed the importin α1−FGF1 complex formation and ERK1/2 activation, resulting in decreased cell growth. This study provides novel evidence that functional importin α1 is located at the cell surface, where it accelerates the proliferation of cancer cells.