摘要:
The present invention is directed to a culture medium for neurons prepared by adding albumin to a culture supernatant obtained from a culture of primary astroglial cells in a trophic medium supplemented with insulin and transferrin. The culture medium of the present invention makes it possible to culture central nerve cells consistently. When they are cultured at a low cell density, neurites extend excellently, and synapses are formed rapidly. On the other hand, when they are cultured at a high cell density, long-term stability of cells that had formed neuronetworks can be obtained.
摘要:
A liquid medium for nerve cells prepared by adding albumin to the culture supernatant of primary astroglia cells obtained by incubating the astroglia cells in a nutritional medium containing insulin and transferrin. By using the liquid medium, central nerve cells can be stably incubated. Thus, in low density incubation, synapses excellent in the elongation of axons can be quickly formed, while, in high density incubation, it is possible to provide cells forming a nervous network and being excellent in the stability over a prolonged storage.