Department of Biological Sciences, Mississippi State University, MS 39762, USA.
Am J Reprod Immunol. 2011 May;65(5):480-91. doi: 10.1111/j.1600-0897.2010.00919.x. Epub 2010 Sep 6.
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-1β), IL-10 (anti-inflammatory), and the chemokine SDF-1α in early- and late-term placental tissues.
Real-time reverse transcriptase PCR was used to measure gene expression in placental tissues.
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-1β and SDF-1α 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-1α expression at both stages and decreased IL-12:IL-10 ratio at late pregnancy.
FIV infection caused a pro-inflammatory placental microenvironment at early, but not late pregnancy.
用 FIV-B-2542 感染猫会导致胎儿感染率和繁殖失败率升高。我们假设,FIV 感染的母猫胎盘细胞因子表达失调,异常表达会加剧炎症并影响妊娠结局。我们的目的是定量检测早期和晚期胎盘组织中代表性促炎细胞因子(IL-6、IL-12p35 和 IL-1β)、IL-10(抗炎)和趋化因子 SDF-1α的表达。
采用实时逆转录 PCR 法检测胎盘组织中的基因表达。
FIV 感染组织在妊娠早期表现出 IL-6 和 IL-12p35 表达增加,IL-10 表达减少;在妊娠晚期,IL-6 表达增加,IL-1β和 SDF-1α表达减少。妊娠晚期,IL-6 表达与 FIV 载量呈正相关。在妊娠早期,感染组织的 IL-12:IL-10 比值较高,但在妊娠晚期则不然。在两个阶段,胎儿失活都伴随着 IL-12p35 和 SDF-1α 表达减少以及妊娠晚期 IL-12:IL-10 比值降低。
FIV 感染在妊娠早期引起促炎胎盘微环境,但在妊娠晚期则不然。