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tel-00435843, version 1 - 24 Nov 2009<br />

Figure S2: Icap-1 +/+ and Icap-1 rescue MEF cells disp<strong>la</strong>y simi<strong>la</strong>r spreading and migration<br />

velocities.<br />

A. Spreading assay of Icap-1 +/+ , Icap-1 −/− , and Icap-1 rescue MEF cells on increasing FN<br />

substrate <strong>de</strong>nsities. Cells were see<strong>de</strong>d on various concentrations of FN-coated surfaces and<br />

were allowed to spread for 1 h. Round and f<strong>la</strong>ttened cells were counted, and spread cells were<br />

expressed as the percentage of total cell number. Each point represents the mean of two<br />

separate experiments, and error bars represent SD. *, P < 0.05.<br />

B. The migration speed of Icap-1 +/+ , Icap-1 −/− , and Icap-1 rescue MEF cells was d<strong>et</strong>ermined on<br />

various FN concentrations using time-<strong>la</strong>pse phase-contrast vi<strong>de</strong>o microscopy and cell tracking<br />

with M<strong>et</strong>aMorph software. 20–40 cells were photographed for each experimental condition at<br />

4-min intervals over an 8-h period. Error bars represent SD from three separate experiments.<br />

The maximal migration speed was used to s<strong>et</strong> up 100% for each cell type.

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