Cytokine Dysregulation in Early- and Late-Term Placentas from Feline Immunodeficiency Virus (FIV)-Infected Cats

被引:8
|
作者
Scott, Veronica L. [1 ]
Boudreaux, Crystal E. [1 ]
Lockett, Nikki N. [1 ]
Clay, Brittany T. [1 ]
Coats, Karen S. [1 ]
机构
[1] Mississippi State Univ, Dept Biol Sci, Mississippi State, MS 39762 USA
基金
美国国家卫生研究院;
关键词
Cytokines; feline immunodeficiency virus; inflammation; placenta; SUCCESSFUL PREGNANCY; TROPHOBLASTIC CELLS; CXCL12; SDF-1-ALPHA; HIV-1; INFECTION; MESSENGER-RNA; CROSS-TALK; T-CELLS; EXPRESSION; FIV; TRANSMISSION;
D O I
10.1111/j.1600-0897.2010.00919.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Problem Experimental infection of cats with FIV-B-2542 produces high rates of fetal infection and reproductive failure. We hypothesized that dysregulation of placental cytokine expression occurs in FIV-infected queens, and aberrant expression potentiates inflammation and impacts pregnancy outcome. Our purpose was to quantify expression of representative pro-inflammatory cytokines (IL-6, IL-12p35, and IL-1 beta), IL-10 (anti-inflammatory), and the chemokine SDF-1 alpha in early- and late-term placental tissues. Method of study Real-time reverse transcriptase PCR was used to measure gene expression in placental tissues. Results Increased expression of IL-6 and IL-12p35 and decreased expression of IL-10 occurred in FIV-infected tissues at early pregnancy; at late gestation, IL-6 expression increased and IL-1 beta and SDF-1 alpha decreased. At late pregnancy, IL-6 expression positively correlated with FIV load. IL-12:IL-10 ratios were higher in infected tissues at early, but not late pregnancy. Fetal non-viability accompanied decreased IL-12p35 and SDF-1 alpha expression at both stages and decreased IL-12:IL-10 ratio at late pregnancy. Conclusion FIV infection caused a pro-inflammatory placental microenvironment at early, but not late pregnancy.
引用
收藏
页码:480 / 491
页数:12
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