Cited 0 times in Scipus Cited Count

Brain inflammation and microglia: facts and misconceptions

DC Field Value Language
dc.contributor.authorJeong, HK-
dc.contributor.authorJi, K-
dc.contributor.authorMin, K-
dc.contributor.authorJoe, EH-
dc.date.accessioned2014-07-11T04:51:10Z-
dc.date.available2014-07-11T04:51:10Z-
dc.date.issued2013-
dc.identifier.issn1226-2560-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/10549-
dc.description.abstractThe inflammation that accompanies acute injury has dual functions: bactericidal action and repair. Bactericidal functions protect damaged tissue from infection, and repair functions are initiated to aid in the recovery of damaged tissue. Brain injury is somewhat different from injuries in other tissues in two respects. First, many cases of brain injury are not accompanied by infection: there is no chance of pathogens to enter in ischemia or even in traumatic injury if the skull is intact. Second, neurons are rarely regenerated once damaged. This raises the question of whether bactericidal inflammation really occurs in the injured brain; if so, how is this type of inflammation controlled? Many brain inflammation studies have been conducted using cultured microglia (brain macrophages). Even where animal models have been used, the behavior of microglia and neurons has typically been analyzed at or after the time of neuronal death, a time window that excludes the inflammatory response, which begins immediately after the injury. Therefore, to understand the patterns and roles of brain inflammation in the injured brain, it is necessary to analyze the behavior of all cell types in the injured brain immediately after the onset of injury. Based on our experience with both in vitro and in vivo experimental models of brain inflammation, we concluded that not only microglia, but also astrocytes, blood inflammatory cells, and even neurons participate and/or regulate brain inflammation in the injured brain. Furthermore, brain inflammation played by these cells protects neurons and repairs damaged microenvironment but not induces neuronal damage.-
dc.language.isoen-
dc.titleBrain inflammation and microglia: facts and misconceptions-
dc.typeArticle-
dc.identifier.urlhttp://en-journal.org/DOIx.php?id=10.5607/en.2013.22.2.59-
dc.subject.keywordbrain inflammation-
dc.subject.keywordmicroglia-
dc.subject.keywordrepair-
dc.contributor.affiliatedAuthor조, 은혜-
dc.type.localJournal Papers-
dc.identifier.doi10.5607/en.2013.22.2.59-
dc.citation.titleExperimental neurobiology-
dc.citation.volume22-
dc.citation.number2-
dc.citation.date2013-
dc.citation.startPage59-
dc.citation.endPage67-
dc.identifier.bibliographicCitationExperimental neurobiology, 22(2). : 59-67, 2013-
dc.identifier.eissn2093-8144-
dc.relation.journalidJ012262560-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Pharmacology
Files in This Item:
10.5607_en.2013.22.2.59.pdfDownload

qrcode

해당 아이템을 이메일로 공유하기 원하시면 인증을 거치시기 바랍니다.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse