Stimulated single-cell force spectroscopy to quantify cell adhesion receptor crosstalk

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Jens Friedrichs - , TUD Dresden University of Technology (Author)
  • Jonne Helenius - , TUD Dresden University of Technology (Author)
  • Daniel J. Müller - , Chair of Cellular Machines (Author)

Abstract

To control their attachment to substrates and other cells, cells regulate their adhesion receptors. One regulatory process is receptor crosstalk, where the binding of one type of cell adhesion molecule influences the activity of another type. To identify such crosstalk and gain insight into their mechanisms, we developed the stimulated single-cell force spectroscopy assay. In this assay, the influence of a cells adhesion to one substrate on the strength of its adhesion to a second substrate is examined. The assay quantifies the adhesion of the cell and the contributions of specific adhesion receptors. This allows mechanisms by which the adhesion is regulated to be determined. Using the assay we identified crosstalk between collagen-binding integrin α 1β1 and fibronectin-binding integrin α5β1 in HeLa cells. This crosstalk was unidirectional, from integrin α5β1 to integrin α5β1, and functioned by regulating the endocytosis of integrin α5β1. The single-cell assay should be expandable for the screening and quantification of crosstalk between various cell adhesion molecules and other cell surface receptors.

Details

Original languageEnglish
Pages (from-to)1455-1462
Number of pages8
JournalProteomics
Volume10
Issue number7
Publication statusPublished - Apr 2010
Peer-reviewedYes

External IDs

PubMed 20127696

Keywords

ASJC Scopus subject areas

Keywords

  • Atomic force microscopy, Cell adhesion, Cell biology, Crosstalk, Integrin, Single-cell force spectroscopy