Journal: Experimental mechanics
Article Title: In situ measurement of native extracellular matrix strain
doi: 10.1007/s11340-019-00499-y
Figure Lengend Snippet: Experimental procedure. a. Decellularization of murine embryonic forelimbs allows the visualization of the extracellular matrix in its native conformation using confocal microscopy, after staining for ECM of interest. Decellularized forelimbs are imaged with an inverted confocal microscope while submerged in PBS. Embryo decellularization panels adapted from [12]. b. Volume images obtained before (cyan) and after load (magenta), corresponding to the same area of the digit, are correlated to extract displacements with fast iterative digital volume correlation (FIDVC). Displacements are analyzed and plotted in color as vector fields. Strain is calculated by fitting each set of displacement values to polynomial functions and then calculating their derivatives analytically, indicated by u(x) and u’(x).
Article Snippet: The intensity arrays of the reference and compressed configurations were compared using the MATLAB-based FIDVC algorithm developed by Bar-Kochba et al. , to extract the displacement fields of the ECM networks [ 13 ].
Techniques: Confocal Microscopy, Staining, Microscopy, Plasmid Preparation