Filamin a modulates kinase activation and intracellular trafficking of epidermal growth factor receptors in human melanoma cells

Jennifer L. Fiori, Tie Nian Zhu, Michael P. O'Connell, Keith S. Hoek, Fred E. Indig, Brittany P. Frank, Christa Morris, Sutapa Kole, Joanne Hasskamp, George Elias, Ashani T. Weeraratna, Michel Bernier

Research output: Contribution to journalArticlepeer-review

Abstract

The actin-binding protein filamin A (FLNa) affects the intracellular trafficking of various classes of receptors and has a potential role in oncogenesis. However, it is unclear whether FLNa regulates the signaling capacity and/or down-regulation of the activated epidermal growth factor receptor (EGFR). Here it is shown that partial knockdown of FLNa gene expression blocked ligand-induced EGFR responses in metastatic human melanomas. To gain greater insights into the role of FLNa in EGFR activation and intracellular sorting, we used M2 melanoma cells that lack endogenous FLNa and a subclone in which human FLNa cDNA has been stably reintroduced (M2A7 cells). Both tyrosine phosphorylation and ubiquitination of EGFR were significantly lower in epidermal growth factor (EGF)-stimulated M2 cells when compared with M2A7 cells. Moreover, the lack of FLNa interfered with EGFR interaction with the ubiquitin ligase c-Cbl. M2 cells exhibited marked resistance to EGF-induced receptor degradation, which was very active in M2A7 cells. Despite comparable rates of EGF-mediated receptor endocytosis, internalized EGFR colocalized with the lysosomal marker lysosome-associated membrane protein-1 in M2A7 cells but not M2 cells, in which EGFR was found to be sequestered in large vesicles and subsequently accumulated in punctated perinuclear structures after EGF stimulation. These results suggest the requirement of FLNa for efficient EGFR kinase activationandthe sorting of endocytosed receptors into the degradation pathway.

Original languageEnglish (US)
Pages (from-to)2551-2560
Number of pages10
JournalEndocrinology
Volume150
Issue number6
DOIs
StatePublished - Jun 2009

ASJC Scopus subject areas

  • Endocrinology

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