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Flexible, actin-based ridges colocalise with the beta1 integrin on the surface of melanoma cells.

Abstract
Using a combination of laser-scanning confocal microscopy and atomic force microscopy, we have identified flexible, actin-based structures on the surface of cells derived from the vertical growth phase of melanoma progression. These flexible structures, lacking on the surface of mature melanocytes, were observed on the surface of all four melanoma cell lines tested. Further investigation revealed that the beta1 integrin colocalises with these actin-based ridges on the cell surface, whereas beta1 integrin distribution in melanocytes did not correlate with actin-based structures. Fibronectin staining on the surface of melanoma cells was partially codistributed with the ridges. The combination of structural information derived from atomic force microscopy images and fluorescent imaging of the distribution of labelled proteins involved in invasion and metastasis has allowed us to identify a common feature that may be involved in disease progression, at the surface of vertical growth phase melanoma cells, despite the known variation in genetic composition of melanoma.
AuthorsK Poole, D Müller
JournalBritish journal of cancer (Br J Cancer) Vol. 92 Issue 8 Pg. 1499-505 (Apr 25 2005) ISSN: 0007-0920 [Print] England
PMID15846299 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Actins
  • Integrin beta Chains
Topics
  • Actins (metabolism, ultrastructure)
  • Cell Adhesion (physiology)
  • Cell Line, Tumor
  • Humans
  • Integrin beta Chains (metabolism, ultrastructure)
  • Melanocytes (ultrastructure)
  • Melanoma (metabolism, ultrastructure)
  • Microscopy, Atomic Force
  • Microscopy, Confocal

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