Original Articles
Copyright ©The Author(s) 2000.
World J Gastroenterol. Jun 15, 2000; 6(3): 365-370
Published online Jun 15, 2000. doi: 10.3748/wjg.v6.i3.365
Figure 1
Figure 1 Hepatocytes growth curve in different culture systems on microcarriers.
Figure 2
Figure 2 Four hours after inoculation cell-bridge could be observed between microcarriers (under phase-contrast microscope × 200).
Figure 3
Figure 3 Microcarriers were arranged as a string of beads by adhered hepatocytes (under phase-contrast microscope × 400).
Figure 4
Figure 4 Stringed microcarriers with adhered hepatocytes (under phase contrast microscope × 730).
Figure 5
Figure 5 Hepatocytes looked like "cell flowers" 24 h after being cultivated in suspension and aggregated spheroids (under phase contrast microscope × 400).
Figure 6
Figure 6 On the d7 hepatocytes aggregated into "cell spheroids" (under phase contrast microscope × 400).
Figure 7
Figure 7 On the d10 hepatocytes in the forms of algoid plants (under phase contrast microscope × 200).
Figure 8
Figure 8 Changes of albumin synthesis in hepatocytes from different culture systems on microcarriers.
Figure 9
Figure 9 Changes of urea secretion in hepatocytes from different culture systems on microcarriers.
Figure 10
Figure 10 Dynamic changes of albumin and urea in the supernatant fluid.