Figure 1
Figure 1. Expression of intact uPAR inversely correlates with cell density. HUVECs were seeded in different densities (indicated as cells per centimeter squared) and grown in complete growth medium for 4 days. Photographs were taken before harvest. (A) Immunocytofluorimetric detections of cell surface uPAR (nonpermeabilized cells; gray line) and total uPAR (permeabilized cells; black line). The total amount of uPAR decreases with cell density. Geometric means for fluorescence intensities were calculated. Filled gray bar represents IgG. Data are mean ± SEM. (B) Relative quantitative reverse transcriptase-polymerase chain reaction of uPAR mRNA normalized to porphobilinogen deaminase. Data are mean ± SEM. *P < .05. (C) Representative Western blot for uPAR of lysates of HUVECs. Mainly intact (ie, full-length) uPAR (∼ 44 kDa) was detected in contrast to cleaved uPAR (30 kDa).

Expression of intact uPAR inversely correlates with cell density. HUVECs were seeded in different densities (indicated as cells per centimeter squared) and grown in complete growth medium for 4 days. Photographs were taken before harvest. (A) Immunocytofluorimetric detections of cell surface uPAR (nonpermeabilized cells; gray line) and total uPAR (permeabilized cells; black line). The total amount of uPAR decreases with cell density. Geometric means for fluorescence intensities were calculated. Filled gray bar represents IgG. Data are mean ± SEM. (B) Relative quantitative reverse transcriptase-polymerase chain reaction of uPAR mRNA normalized to porphobilinogen deaminase. Data are mean ± SEM. *P < .05. (C) Representative Western blot for uPAR of lysates of HUVECs. Mainly intact (ie, full-length) uPAR (∼ 44 kDa) was detected in contrast to cleaved uPAR (30 kDa).

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