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pubmed-article:21513770pubmed:abstractTextMethylmercury (MeHg) is a neurotoxin capable of causing severe damage to the CNS, especially in the developing fetus. Glia in the CNS release a number of cytokines that are important for proper CNS development and function. We reported earlier that MeHg could induce interleukin-6 (IL-6) release in primary mouse glia. This finding is significant considering previous reports indicating that sustained IL-6 exposure could be detrimental to cerebellar granule neurons, one of the major cellular targets of MeHg cytotoxicity. By using pharmacological antagonists against phophatidycholine- and phosphoinositol-specific phospholipase C, the current study indicated that phospholipase C activity was necessary for MeHg-induced IL-6 release. Results from pharmacological antagonists further suggested that the calcium signaling initiated by phospholipase C appeared essential for this event. In contrast, protein kinase C activity did not appear to be important. Even though mitogen-activated protein kinases were important for IL-6 release in some experimental systems, these enzymes did not appear to be required for MeHg-induced IL-6 release in glia. Based on these data and those reported by us and others, there is a possibility that MeHg-induced phospholipase C activation initiates a calcium signaling that causes phospholipase A(2) activation. This, in turn, leads to arachidonic acid and lysophosphatidyl choline generation, both of which are potent inducers for IL-6 release.lld:pubmed
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pubmed-article:21513770pubmed:authorpubmed-author:ChangJason...lld:pubmed
pubmed-article:21513770pubmed:copyrightInfoCopyright © 2011 Elsevier Ireland Ltd. All rights reserved.lld:pubmed
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pubmed-article:21513770pubmed:pagination152-6lld:pubmed
pubmed-article:21513770pubmed:dateRevised2011-9-26lld:pubmed
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pubmed-article:21513770pubmed:articleTitleMethylmercury-induced IL-6 release requires phospholipase C activities.lld:pubmed
pubmed-article:21513770pubmed:affiliationDepartment of Neurobiology and Developmental Sciences, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USA. changjasony@uams.edulld:pubmed
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