Quantitative mapping of averaged focal adhesion dynamics in migrating cells by shape normalization
Author(s) -
Christoph Möhl,
Norbert Kirchgeßner,
Claudia Schäfer,
Bernd Hoffmann,
Rudolf Merkel
Publication year - 2012
Publication title -
journal of cell science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.384
H-Index - 278
eISSN - 1477-9137
pISSN - 0021-9533
DOI - 10.1242/jcs.090746
Subject(s) - focal adhesion , vinculin , biology , actin , tractive force , cell adhesion , ptk2 , adhesion , lim domain , microbiology and biotechnology , dynamics (music) , biophysics , cell , phosphorylation , materials science , biochemistry , physics , thermodynamics , mitogen activated protein kinase kinase , protein kinase a , gene , zinc finger , composite material , transcription factor , acoustics
The spatially ordered formation and disassembly of focal adhesions is a basic requirement for effective cell locomotion. Because focal adhesions couple the contractile actin-myosin network to the substrate, their distribution determines the pattern of traction forces propelling the cell in a certain direction. In the present study, we quantitatively analyzed the spatial patterning of cell-substrate adhesion in migrating cells by mapping averaged focal adhesion growth dynamics to a standardized cell coordinate system. These maps revealed distinct zones of focal adhesion assembly, disassembly and stability and were strongly interrelated with corresponding actin flow and traction force patterns. Moreover, the mapping technique enables precise detection of even minute responses of adhesion dynamics upon targeted signaling perturbations. For example, the partial inhibition of vinculin phosphorylation was followed by the reduced number of newly formed adhesions, whereas growth dynamics of existing adhesions remained unaffected.
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