Single-Cell Acoustic Force Spectroscopy: Resolving Kinetics and Strength of T Cell Adhesion to Fibronectin
Author(s) -
Douwe Kamsma,
Pascal Bochet,
Felix Oswald,
Nander Alblas,
Sophie Goyard,
Gijs J. L. Wuite,
Erwin J.G. Peterman,
Thierry Rose
Publication year - 2018
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2018.08.034
Subject(s) - fibronectin , adhesion , force spectroscopy , kinetics , extracellular matrix , cell adhesion , biophysics , microbiology and biotechnology , chemistry , cell adhesion molecule , cell , materials science , nanotechnology , biology , physics , atomic force microscopy , biochemistry , organic chemistry , quantum mechanics
Assessing the strength and kinetics of molecular interactions of cells with the extracellular matrix is fundamental to understand cell adhesion processes. Given the relevance of these processes, there is a strong need for physical methods to quantitatively assess the mechanism of cell adhesion at the single-cell level, allowing discrimination of cells with different behaviors. Here we introduce single-cell acoustic force spectroscopy (scAFS), an approach that makes use of acoustic waves to exert controlled forces, up to 1 nN, to hundreds of individual cells in parallel. We demonstrate the potential of scAFS by measuring adhesion forces and kinetics of CD4 + T lymphocytes (CD4) to fibronectin. We determined that CD4 adhesion is accelerated by interleukin-7, their main regulatory cytokine, whereas CD4 binding strength remains the same. Activation of these cells likely increases their chance to bind to the vessel wall in the blood flow to infiltrate inflamed tissues and locally coordinate the immune response.
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