Copper modulates the phenotypic response of activated BV2 microglia through the release of nitric oxide

• Published in: Nitric oxide Vol. 27; no. 4; pp. 201 - 209
• Main Authors: Rossi-George, Alba, Guo, Chang-Jiang, Oakes, Benjamin L., Gow, Andrew J.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.12.2012
• Subjects: Animals; Cell Line; Cell Survival; Copper; Copper - pharmacology; Fluorescent Antibody Technique; Inflammation - metabolism; Inflammation Mediators - metabolism; Macrophage phenotype; Mice; Microglia; Microglia - metabolism; Neurodegeneration; Neurodegenerative Diseases - metabolism; Nitric oxide; Nitric Oxide - metabolism; Phenotype; Macrophage phenotype; Copper; Neurodegeneration; Nitric oxide; Microglia
• ISSN: 1089-8603; 1089-8611
• DOI: 10.1016/j.niox.2012.07.002

► Cu(I) has minimal morphologic and phenotypic effects on unstimulated BV2 microglia. ► Cu(I) inhibits nitrite release in LPS-stimulated microglia. ► Cu(I)-induced NO2 inhibition is not due to altered protein or RNA NOS expression. ► Cu(I) affects the morphology of LPS-stimulated BV2 cells. Microglia are resident immune cells of the central nervous system. Their persistent activation in neurodegenerative diseases, traditionally attributed to neuronal dysfunction, may be due to a microglial failure to modulate the release of cytotoxic mediators such as nitric oxide (NO). The persistent activation of microglia with the subsequent release of NO vis-á-vis the accumulation of redox transition metals such as copper (Cu) in neurodegenerative diseases, prompted the hypothesis that copper would alter NO signaling by changing the redox environment of the cell and that, by altering the fate of NO, microglia would adopt a different phenotype. We have used the microglial cell model, BV2, to examine the effects of Cu(I) on NO production and activation as they have been shown to be phenotypically plastic. Our results show that cell viability is not affected by Cu(I) in BV2 microglia and that it has no effect on iNOS mRNA, protein expression and nitrite release. However, when LPS is added to Cu(I)-treated medium, nitrite release is abrogated while iNOS expression is not significantly altered. This effect is Cu(I)-specific and it is not observed with other non-redox metals, suggesting that Cu(I) modulates NO reactivity. Immunofluorescence analysis shows that the M1 (inflammatory) phenotype of BV2 microglia observed in response to LPS, is shifted to an M2 (adaptive) phenotype when Cu(I) is administered in combination with LPS. This same shift is not observed when iNOS function is inhibited by 1400W. In the present study we show that Cu(I) modulates the release of NO to the media, without altering iNOS expression, and produces phenotypic changes in BV2 microglia.