10 research outputs found

    IFN-gamma Impairs Release of IL-8 by IL-1beta-stimulated A549 Lung Carcinoma Cells

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    Background Production of interferon (IFN)-gamma is key to efficient anti-tumor immunity. The present study was set out to investigate effects of IFNgamma on the release of the potent pro-angiogenic mediator IL-8 by human A549 lung carcinoma cells. Methods A549 cells were cultured and stimulated with interleukin (IL)-1beta alone or in combination with IFNgamma. IL-8 production by these cells was analyzed with enzyme linked immuno sorbent assay (ELISA). mRNA-expression was analyzed by real-time PCR and RNase protection assay (RPA), respectively. Expression of inhibitor-kappaBalpha, cellular IL-8, and cyclooxygenase-2 was analyzed by Western blot analysis. Results Here we demonstrate that IFNgamma efficiently reduced IL-8 secretion under the influence of IL-1beta. Surprisingly, real-time PCR analysis and RPA revealed that the inhibitory effect of IFNgamma on IL-8 was not associated with significant changes in mRNA levels. These observations concurred with lack of a modulatory activity of IFNgamma on IL-1beta-induced NF-kappaB activation as assessed by cellular IkappaB levels. Moreover, analysis of intracellular IL-8 suggests that IFNgamma modulated IL-8 secretion by action on the posttranslational level. In contrast to IL-8, IL-1beta-induced cyclooxygenase-2 expression and release of IL-6 were not affected by IFNgamma indicating that modulation of IL-1beta action by this cytokine displays specificity. Conclusions Data presented herein agree with an angiostatic role of IFNgamma as seen in rodent models of solid tumors and suggest that increasing T helper type 1 (Th1)-like functions in lung cancer patients e.g. by local delivery of IFNgamma may mediate therapeutic benefit via mechanisms that potentially include modulation of pro-angiogenic IL-8

    China as Chimney of the World: The Fossil Capital Hypothesis

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    What has caused the early 21st-century emissions explosion in China? Driving a global explosion, it appears to stand in some relation to processes of globalization, but these links have mostly remained unexplored. This article revisits some established frameworks for understanding the connection between globalization and environmental degradation and argues that they are insufficient for explaining the Chinese explosion. A new hypothesis is outlined, called "the fossil capital hypothesis." It proposes that globally mobile capital will tend to relocate production to countries with cheap and disciplined labor, but only through the accelerated consumption of fossil energy. Via three specified "effects," the inflow of global capital will therefore set off massive increases in CO2 emissions. The hypothesis is applied in a brief analysis of developments in China between 2001 and 2008, and in other Asian countries after the Chinese strike wave in 2010

    Abstracts from the 8th International Congress of the Asia Pacific Society of Infection Control (APSIC)

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