Fig. 8 Nephronectin promotes HUVEC migration, tube formation, and stabilization in vitro. A, Cell migration assay: representative brightfield images of wound assays 1 and 6 hours after scratching. Cells were cultured on gelatin? (control) or mr?NPNT?coated 24?well cell culture plates. B, Quantitative analysis of cell migration (n=4). The mean value of the control was considered 100% in each case. C, Tube formation assay: representative brightfield images of HUVECs cultured on Matrigel with BSA (10 ?g/mL, control) or mr?NPNT (10??g/mL) at 4 and 22 hours after seeding. D?F, Quantitative analysis of tube branching (D), and tube stability (E, F) (n=4). Mean value of the control was considered 100% in each case. Statistical significance was determined by a 2?tailed Student's t test. Data are meanąSEM. ns: P>0.05. *P?0.05. HUVEC indicates human umbilical vascular endothelial cell; and mr?NPNT, recombinant mouse nephronectin.
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