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Fig. 3. Inhibition of MK-induced neurite outgrowth by anti-{alpha}6-integrin antibody. Plastic 24-well culture plates were coated with 10 µg ml–1 of MK for 2 hours at room temperature. Then, a grid pattern was made by the ultraviolet-inactivation technique using electron-microscopy grids. After blocking with 10 mg ml–1 BSA, brain cells (1x106) from mouse embryonic cerebral cortex were cultured without further addition (A) or with 0.0045% NaN3 (B), 50 µg ml–1 anti-{alpha}4-integrin antibody (C) or anti-{alpha}6-integrin antibody (D) at 37°C under an atmosphere containing 5% CO2. (E) Effects of anti-{alpha}6-integrin antibody on neurite outgrowth on wells coated with 20 µg ml–1 MK. The proportion of neurons with a defined neurite length was determined by enumerating cells in ten fields at 400x magnification. The average value obtained in three different wells is shown with the s.d. Phase-contrast photomicrographs were taken after culture for 48 hours using a Nikon DIAPHOTO and Olympus CCD camera C5530. Scale bar, 50 µm.





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