4.4 Article

Evaluating lipopolysaccharide-induced oxidative stress in bovine granulosa cells

Journal

JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
Volume 34, Issue 12, Pages 1619-1626

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10815-017-1031-2

Keywords

Granulosa cell; Oxidative stress; Lipopolysaccharide; Peripheral blood mononuclear cell; Reactive oxygen

Funding

  1. Eunice Kennedy Shriver National Institute of Child Health & Human Development of the National Institutes of Health [R01HD084316]

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The purpose of this study was to evaluate the capacity of bovine granulosa cells to generate reactive oxygen intermediates in response to lipopolysaccharide. We hypothesized that granulosa cells increase reactive oxygen intermediates in response to Gram-negative lipopolysaccharide in a similar manner to immune cells. Bovine peripheral blood mononuclear cells and granulosa cells were cultured in the presence of lipopolysaccharide. Oxidative stress was evaluated using the fluorescent marker dye CellROX, and oxidative stress-related genes were measured using real-time RT-PCR. As expected, peripheral blood mononuclear cells increased oxidative stress in response to lipopolysaccharide as measured by accumulation of the fluorescent marker dye CellROX. While granulosa cells demonstrate the capacity to increase accumulation of CellROX dye in response to a positive control menadione, lipopolysaccharide had no effect on accumulation of CellROX dye. The expression of GSR, SOD1, and SOD2 were variable in peripheral blood mononuclear cells treated with lipopolysaccharide but were consistently upregulated when co-incubated with the antioxidant, N-acetyl cysteine. The expression of oxidative stressArelated genes was not altered in granulosa cells, with the exception of elevated SOD1 following lipopolysaccharide exposure in the absence of antioxidant. Combined, these data suggest that while reactive stress is important in pathogen killing and inflammation in immune cells, granulosa cells do not increase oxidative stress in response to lipopolysaccharide.

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