Using morphological, immunocytochemical, and functional parameters we have previously shown that highly purified adult rat microglial cells undergo a process of "activation" when cultured in a serum-containing medium in the absence of added proinflammatory substances or other factors (Slepko and Lev
Progressive activation of adult microglial cells in vitro
β Scribed by Natalia Slepko; Giulio Levi
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 691 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0894-1491
No coin nor oath required. For personal study only.
β¦ Synopsis
Bulk-isolated microglial cells from the adult rat brain grown in N2 medium supplemented with 10% fetal calf serum survived for at least 2 weeks, and their purity was > 99% at day 1 and > 93% at day 7. The phenotype of freshly plated cells was comparable to that of "resting," ramified microglia in vivo. With time in culture and with different schedules, depending on the parameter considered, microglia acquired antigenic (e.g., positivity for vimentin, ED1, major histocompatibility complex class I antigens, leukocyte common antigen, and to a lesser extent CD4) and functional (e.g., proliferation, phagocytosis) features characteristic of "activated" microglia as described in situ. Production of nitrite and prostaglandin E2 in response to lipopolysaccharide increased greatly with time in culture. Phagocytosis was also accompanied by increased release of nitrite and prostaglandin ES, the latter being more affected than the first by the age of the cultures. The culture system described may be suitable to study the factors that can modulate "activation" of adult microglia. D 1996 Wiley-Liss, Inc.
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