| Literature DB >> 16406093 |
Michal Schwartz1, Oleg Butovsky, Wolfgang Brück, Uwe-Karsten Hanisch.
Abstract
Microglia, the standby cells for immune defense in the CNS, have a reputation for exacerbating the neural damage that occurs in neurodegenerative diseases. However, research over the past few years has established that microglia do not constitute a single, uniform cell population, but rather comprise a family of cells with diverse phenotypes--some that are beneficial and others that the CNS can barely tolerate and that are therefore destructive. This finding raised several questions. What instructs microglia to acquire a particular phenotype, and how do these phenotypes differ? How committed are microglia to a specific phenotype? Can destructive microglia become protective, and can protective microglia retain their beneficial phenotype even when they encounter a destructive environment? Here, we address these questions, and the background of research that elicited them.Entities:
Mesh:
Year: 2006 PMID: 16406093 DOI: 10.1016/j.tins.2005.12.005
Source DB: PubMed Journal: Trends Neurosci ISSN: 0166-2236 Impact factor: 13.837