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EXTRACELLULAR ATP REGULATES IL-1BETA RELEASE FROM MICROGLIAL CELLS VIA
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TitleEXTRACELLULAR ATP REGULATES IL-1BETA RELEASE FROM MICROGLIAL CELLS VIA
AuthorLiang, Chengya
KeywordsBiomedical Sciences -- Dissertations, Academic
Dissertations, Academic -- Biomedical Sciences
ATP
IL 1[beta]
Microglia
AbstractTraumatic brain injury (TBI) induces a state of microglialactivation, which includes upregulation of macrophage functions and release inflammatory mediators such as certain inflammatory cytokines. Current literature suggests that interleukin-1?; is an important cytokine mediator, which is dramatically increased after brain injury. Previous studies indicate that ATP is released by traumatically injured astrocytes and serves as a cell-to-cell mediator through purinergic receptors after in vitro injury. However, the mechanism of interleukin-1?; release after traumatic brain injury remains poorly defined and is difficult to study using in vivo models. Using an in vitro model for traumatic brain injury (cell strain or stretch), we investigated the role of the extracellular nucleotides (ATP) in regulation of interleukin-1?; release in rat cortical brain cells.We now report that activated microglia constitute the major source of interleukin-1?; release after in vitro trauma. ATP is a powerful stimulus for interleukin-1?; release from microglial cultures. Glutamate inhibits interleukin-1?; release. ATP-induced interleukin-1?; release was blocked completely by the P2X7 receptor antagonist, oxidized ATP, and partially by the P2X7 receptor antagonist suramin, suggesting that ATP stimulates interleukin-1â release from microglia via purinergic receptor and the P2X7 receptor is responsible for the interleukin-1?; release. Blockage of interleukin-1?; release by the purinergic receptor antagonists oATP and suramin decreased cell damage in uninjured mixed organotypic brain cell culture exposed to activated microglia. Taken together, these results suggest that interleukin-1?; mediated inflammatory events are regulated in activated microglia by extracellular nucleotides (ATP) via purinergic receptors in central nervous system after in vitro trauma.
AdviserRzigalinski, Beverly
PublisherUniversity of Central Florida
DegreeM.S.
Degree DisciplineDepartment of Molecular Biology and Microbiology
Degree GrantorBurnett College of Biomedical Sciences
Degree ProgramMolecular Biology and Microbiology
Graduation Date2004-08-01
TypeMaster's thesis
Access LevelPublic - Allow Worldwide Access
Release Date2004-08-01
RepositoryUniversity Archives
Repository CollectionElectronic Theses and Dissertations
IdentifierCFE0000133
Access Linkhttp://purl.fcla.edu/fcla/etd/CFE0000133

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