Video 2.

HUVEC migration on 8.7 kPa 2D PA substrates. Montage of time-lapse movies of HUVECs treated with either DMSO control (left), 20 µM Taxol (middle), or 20 µM nocodazole (right) were acquired a spinning disc confocal microscope (TE2000; Nikon) and a 20× 0.45 NA objective lens (Nikon). Images were acquired for 15 h (with a frame taken every 15 min) beginning 60 min after addition of the drug. Bar, 50 µm.


Distinct ECM mechanosensing pathways regulate microtubule dynamics to control endothelial cell branching morphogenesis

Kenneth A. Myers, Kathryn T. Applegate, Gaudenz Danuser, Robert S. Fischer, and Clare M. Waterman

DOI: 10.1083/jcb.201006009
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