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首页> 外文期刊>Placenta >Novel model of placental tissue explants infected by cytomegalovirus reveals different permissiveness in early and term placentae and inhibition of indoleamine 2,3-dioxygenase activity.
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Novel model of placental tissue explants infected by cytomegalovirus reveals different permissiveness in early and term placentae and inhibition of indoleamine 2,3-dioxygenase activity.

机译:巨细胞病毒感染的胎盘组织外植体的新型模型揭示了早期和足月胎盘的不同允许性以及对吲哚胺2,3-双加氧酶活性的抑制。

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Human cytomegalovirus (HCMV) is the most common cause of viral intrauterine infection. Placental infection suggests hematogenous spread and permissiveness may vary according to the age of pregnancy. We set up and investigate permissivity of early and term placenta to HCMV with an ex vivo model of placental histocultures and evaluate the activity profile of IDO. Fourteen first trimester placentae were obtained following elective abortion and twelve term placentae after elective caesarean section. Fresh placental chorionic villi were isolated, washed and distributed on collagen sponge gels after overnight incubation with the virus. The culture medium was collected and fresh medium renewed regularly. Histology and immunohistochemistry showed preserved villous integrity in cultured placental histocultures. Infection could be seen in tissue sections of both early and term placentae, although early placentae were more permissive. Indoleamine 2,3-dioxygenase (IDO) is highly expressed in the placenta and is known to prevent maternal immune rejection. Constitutive IDO activity was higher in early, compared to term placentae and HCMV infection inhibited IDO activity in early placentae. IFN-gamma-induced IDO activity was suppressed by HCMV in both early and term placentae. Our work shows a novel method of placenta organ culture. Our findings suggest that HCMV infects early placentae more strongly than term placentae. Early placental dysfunction through the inhibition of IDO activity may reveal a possible mechanism for miscarriages.
机译:人巨细胞病毒(HCMV)是病毒性子宫内感染的最常见原因。胎盘感染提示血源性扩散和允许性可能随怀孕年龄而异。我们使用胎盘组织培养的体外模型建立和调查早期和足月胎盘对HCMV的容许性,并评估IDO的活性。选择性流产后获得十四个早孕胎盘,选择性剖腹产后获得十二个胎盘。与病毒孵育过夜后,将新鲜的胎盘绒毛膜绒毛分离,洗涤并分配在胶原海绵凝胶上。收集培养基并定期更新新鲜培养基。组织学和免疫组化显示在培养的胎盘组织培养物中保留了绒毛完整性。尽管早期胎盘的允许性更高,但在早期胎盘和足月胎的组织切片中都可以看到感染。吲哚胺2,3-二加氧酶(IDO)在胎盘中高度表达,已知可以预防母体免疫排斥。与足月胎盘相比,本构性IDO活性在早期较高,而HCMV感染抑制了早期胎盘的IDO活性。 HCMV在早期和足月胎盘中均抑制了IFN-γ诱导的IDO活性。我们的工作展示了一种胎盘器官培养的新方法。我们的发现表明,HCMV比足月胎盘感染早期胎盘的能力更强。通过抑制IDO活性早期胎盘功能障碍可能揭示了流产的可能机制。

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