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. 2008 May 15;123(1-2):90-6.
doi: 10.1016/j.vetimm.2008.01.014. Epub 2008 Jan 19.

Expression of CD134 and CXCR4 mRNA in term placentas from FIV-infected and control cats

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Expression of CD134 and CXCR4 mRNA in term placentas from FIV-infected and control cats

Veronica L Scott et al. Vet Immunol Immunopathol. .

Abstract

Feline immunodeficiency virus (FIV) causes a natural infection of domestic cats that resembles HIV-1 in pathogenesis and disease progression. Feline AIDS is characterized by depression of the CD4+ T cell population and fatal opportunistic infections. Maternal-fetal transmission of FIV readily occurs under experimental conditions, resulting in infected viable kittens and resorbed or arrested fetal tissues. Although both FIV and HIV use the chemokine receptor CXCR4 as a co-receptor, FIV does not utilize CD4 as the primary receptor. Rather, CD134 (OX40), a T cell activation antigen and co-stimulatory molecule, is the primary receptor for FIV. We hypothesized that placental expression of CD134 and CXCR4 may render the placenta vulnerable to FIV infection, possibly facilitating efficient vertical transmission of FIV, and impact pregnancy outcome. The purpose of this project was to quantify the relative expression of CD134 and CXCR4 mRNA from the term placentas of three groups of cats: uninfected queens producing viable offspring, experimentally-infected queens producing only viable offspring, and experimentally-infected queens producing viable offspring among mostly non-viable fetuses. Total RNA was extracted from term placental tissues from all groups of cats. Real-time one-step reverse transcriptase-PCR was used to measure gene expression. The FIV receptors CD134 and CXCR4 were expressed in all late term feline placental tissues. Placentas from FIV-infected queens producing litters of only viable offspring expressed more CD134 and CXCR4 mRNA than those from uninfected queens, suggesting that infection may cause upregulation of the receptors. On the other hand, placentas from FIV-infected cats with non-successful pregnancies expressed similar levels of CD134 mRNA and slightly less CXCR4 mRNA than those from uninfected queens. Thus, it appears that cells expressing these receptors may play a role in pregnancy maintenance.

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Fig. 1
Fig. 1
Percentage change in FIV receptor mRNA expression in control versus treated comparisons. (A) Percentage change in CD134 and CXCR4 mRNA in placentas from infected queens producing litters of viable offspring (Group 2) compared to control cats (Group 1); (B) Percentage change in CD134 and CXCR4 mRNA in placentas from Group 1 cats compared to infected queens producing viable offspring among majority non-viable litters (Group 3). Results are shown as 95% upper (+) and lower (−) confidence intervals around the mean (○). Relative expression was 100% if the mRNA expression between the two sample sets was the same.

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