4.4 Article

Ovine trophoblast is a primary source of TNF alpha during Chlamydophila abortus infection

期刊

JOURNAL OF REPRODUCTIVE IMMUNOLOGY
卷 80, 期 1-2, 页码 49-56

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jri.2008.12.003

关键词

Trophoblast; Chlamydophila abortus; TNF alpha; CXCL8; Infectious abortion

资金

  1. Scottish Government Rural and Environment Research and Analysis Directorate (RERAD)
  2. Biological and Biotechnology Sciences Research Council (BBSRC)/RERAD Immunological Toolbox [BBS/B/00255, MRI/094/04]
  3. Biotechnology and Biological Sciences Research Council [BBS/B/00255] Funding Source: researchfish

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Chlamydophila abortus is a Grain-negative obligate intracellular bacterium that causes infectious abortion in sheep (ovine enzootic abortion, OEA) and humans. Infected placentas recovered from sheep that experience OEA have thickened membranes, contain dense inflammatory cellular infiltrates and show evidence of intravascular thrombosis. Despite widespread inflammation, chlamydial multiplication is restricted to the chorionic trophoblast cells. To investigate the potential role of trophoblast in the initiation and propagation of placental inflammation during OEA, the AH-1 ovine trophoblast cell line was experimentally infected with C abortus and analysed for the release of pro-inflammatory mediators. C abortus was found to induce the release of both tumour necrosis factor-alpha (TNF alpha) and CXCL8 (interleukin-8) from AH-1 cells in a dose- and time-dependent manner. Ultra-violet (UV)-killed organisms did not elicit this profile, indicating that intracellular multiplication of C. abortus was required for release of these pro-inflammatory mediators. Exposure of AH-1 cells to recombinant ovine TNF alpha alone resulted in the release of CXCL8, suggestive of a self-propagating inflammatory cytokine and chemokine cascade. These data indicate a primary role for trophoblast in the initiation and propagation of placental inflammation during chlamydial abortion. (C) 2009 Elsevier Ireland Ltd. All rights reserved.

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