4.5 Article

Cell surface localised Hsp70 is a cancer specific regulator of clathrin-independent endocytosis

Journal

FEBS LETTERS
Volume 589, Issue 19, Pages 2747-2753

Publisher

WILEY-BLACKWELL
DOI: 10.1016/j.febslet.2015.07.037

Keywords

Hsp70; Endocytosis; Cancer; Membrane; Clustering

Funding

  1. European Regional Development Fund (EFRE), the state of Upper Austria
  2. Hungarian Basic Research Fund (OTKA) [100857]

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The stress inducible heat shock protein 70 (Hsp70) is present specifically on the tumour cell surface yet without a pro-tumour function revealed. We show here that cell surface localised Hsp70 (sHsp70) supports clathrin-independent endocytosis (CIE) in melanoma models. Remarkably, ability of Hsp70 to cluster on lipid rafts in vitro correlated with larger nano-domain sizes of sHsp70 in high sHsp70 expressing cell membranes. Interfering with Hsp70 oligomerisation impaired sHsp70-mediated facilitation of endocytosis. Altogether our findings suggest that a sub-fraction of sHsp70 co-localising with lipid rafts enhances CIE through oligomerisation and clustering. Targeting or utilising this tumour specific mechanism may represent an additional benefit for anti-cancer therapy. (C) 2015 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

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