4.4 Article

Viral ssRNA Induces First Trimester Trophoblast Apoptosis through an Inflammatory Mechanism

Journal

AMERICAN JOURNAL OF REPRODUCTIVE IMMUNOLOGY
Volume 64, Issue 1, Pages 27-37

Publisher

WILEY-BLACKWELL
DOI: 10.1111/j.1600-0897.2010.00817.x

Keywords

caspase; infection; pregnancy; ssRNA; Toll-like receptor; virus

Funding

  1. Eunice Kennedy Shriver, NICHD, NIH [RO1HD049446, P01HD054713]
  2. Perinatology Research Branch, Division of Intramural Research, Eunice Kennedy Shriver, NICHD, NIH [3N01 HD23342]

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Problem Infection during pregnancy represents a significant cause of mobility and mortality. While viruses pose a major threat, little is known about their effect on early pregnancy, or the mechanisms involved. The objective of this study was to characterize the trophoblast response following exposure to viral ssRNA. Method of study First trimester trophoblast cells were treated with or without viral ssRNA. Cytokine production was measured using multiplex analysis and ELISA. Apoptosis was determined using Hoechst staining, cell viability, and caspase activity assays. Results Treatment of trophoblasts with viral ssRNA increased their secretion of IL-8, IL-6, and IFN beta. However, the ssRNA also induced trophoblast apoptosis. To test whether the viral ssRNA-induced inflammatory response was responsible for this induction of apoptosis, conditioned media (CM) from trophoblasts were added to a fresh culture of cells. The CM from viral ssRNA-treated induced higher levels of trophoblast apoptosis than the control CM. Moreover, recombinant IFN beta induced trophoblast apoptosis. Conclusion We demonstrate that viral ssRNA induces a pro-inflammatory and type I interferon response in the trophoblast and this inflammatory process may indirectly induce trophoblast apoptosis. These results provide a novel mechanism by which certain viral infections might compromise placental integrity and function, and therefore, pregnancy outcome.

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