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Inflammatory Signalling in Fetal Membranes: Increased Expression Levels of TLR 1 in the Presence of Preterm Histological Chorioamnionitis

机译:胎膜的炎症信号:早发组织学绒毛膜羊膜炎存在下TLR 1表达水平的增加。

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摘要

Histological chorioamnionitis (HCA) is an established marker of ascending infection, a major cause of preterm birth. No studies have characterised the global change in expression of genes involved in the toll-like receptor (TLR) signalling pathways in the presence of HCA in the setting of preterm birth (pHCA). Fetal membranes were collected immediately after delivery and underwent histological staging for inflammation to derive 3 groups; term spontaneous labour without HCA (n = 9), preterm birth <34 weeks gestation without HCA (n = 8) and pHCA <34 weeks (n = 12). Profiling arrays ran in triplicate for each group were used to determine the expression of 84 genes associated with TLR signalling and screen for genes of interest (fold change >2; p<0.1). Expression of identified genes was validated individually for all samples, relative to GAPDH, using RT-PCR. Expression of TLR 1, TLR 2, lymphocyte antigen 96, interleukin 8 and Interleukin-1 receptor-associated kinase-like 2 was increased in pHCA (p<0.05). Degree of expression was positively associated with histological staging of both maternal and fetal inflammation (p<0.05). The inflammatory expression profile at the maternal/fetal interface associated with pHCA, a reflection of ascending infection, is extremely heterogeneous suggesting polymicrobial involvement with activation of a common pathway. Antagonism of TLR 1 and TLR 2 signalling in this setting warrants further assessment.
机译:组织学绒毛膜羊膜炎(HCA)是上升感染的确定标志,上升感染是早产的主要原因。在早产(pHCA)的情况下,在HCA存在的情况下,尚未有研究鉴定涉及Toll样受体(TLR)信号通路的基因表达的总体变化。分娩后立即收集胎膜并进行组织学分期进行炎症分3组。无HCA的足月自然分娩(n = 9),无HCA的早产<34周(n = 8)和pHCA <34周(n = 12)。每组一式三份的分析阵列用于确定与TLR信号转导相关的84个基因的表达并筛选感兴趣的基因(倍数变化> 2; p <0.1)。使用RT-PCR,相对于GAPDH,对所有样品分别验证了已鉴定基因的表达。在pHCA中,TLR 1,TLR 2,淋巴细胞抗原96,白细胞介素8和白细胞介素-1受体相关激酶样2的表达增加(p <0.05)。表达水平与母亲和胎儿炎症的组织学分期呈正相关(p <0.05)。与pHCA相关的母体/胎儿界面的炎性表达特征(感染的上升反映)非常不均一,提示多微生物参与了共同途径的激活。在这种情况下,TLR 1和TLR 2信号的拮抗作用值得进一步评估。

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