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Identification of Chemokines Associated with the Recruitment of Decidual Leukocytes in Human Labour: Potential Novel Targets for Preterm Labour

机译:与人类劳动中蜕膜白细胞募集相关的趋化因子的鉴定:早产的潜在新型靶标

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摘要

Current therapies for preterm labour (PTL) focus on arresting myometrial contractions but are largely ineffective, thus alternative therapeutic targets need to be identified. Leukocytes infiltrate the uterus around the time of labour, and are in particularly abundant in decidua (maternal-fetal interface). Moreover, decidual inflammation precedes labour in rat pregnancies and thus may contribute to initiation of labour. We hypothesized that chemokines mediate decidual leukocyte trafficking during preterm labour (PTL) and term labour (TL), thus representing potential targets for preventing PTL. Women were recruited into 4 groups: TL, term not in labour (TNL), idiopathic PTL and PTL with infection (PTLI). Choriodecidual RNA was subjected to a pathway-specific PCR array for chemokines. Differential expression of 12 candidate chemokines was validated by real time RT-PCR and Bioplex assay, with immunohistochemistry to confirm cellular origin. 25 chemokines were upregulated in choriodecidua from TL compared to TNL. A similar pattern was detected in PTL, however a distinct profile was observed in PTLI consistent with differences in leukocyte infiltration. Upregulation of CCL2, CCL4, CCL5, CXCL8 and CXCL10 mRNA and protein was confirmed in TL, with CCL8 upregulated in PTL. Significant correlations were detected between these chemokines and decidual leukocyte abundance previously assessed by immunohistochemical and image analysis. Chemokines were primarily expressed by decidual stromal cells. In addition, CXCL8 and CCL5 were significantly elevated in maternal plasma during labour, suggesting chemokines contribute to peripheral inflammatory events during labour. Differences in chemokine expression patterns between TL and idiopathic PTL may be attributable to suppression of chemokine expression by betamethasone administered to women in PTL; this was supported by in vitro evidence of chemokine downregulation by clinically relevant concentrations of the steroid. The current study provides compelling evidence that chemokines regulate decidual leukocyte recruitment during labour. The 6 chemokines identified represent potential novel therapeutic targets to block PTL.
机译:当前的早产(PTL)疗法专注于阻止子宫肌层收缩,但效果不佳,因此需要确定其他治疗靶点。白细胞在分娩时渗透到子宫中,并且在蜕膜(母胎界面)中尤其丰富。此外,蜕膜炎症在大鼠怀孕之前先于分娩,因此可能有助于引产。我们假设趋化因子在早产(PTL)和足月分娩(TL)期间介导蜕膜白细胞的运输,因此代表了预防PTL的潜在目标。将女性分为4组:TL,非劳动任期(TNL),特发性PTL和感染性PTL(PTLI)。绒毛膜蜕膜的RNA进行趋化因子的途径特异性PCR阵列。通过实时RT-PCR和Bioplex测定法验证了12种候选趋化因子的差异表达,并用免疫组织化学确认了细胞起源。与TNL相比,TL中的25种趋化因子上调。在PTL中检测到了相似的模式,但是在PTLI中观察到了与白细胞浸润差异一致的独特特征。在TL中证实了CCL2,CCL4,CCL5,CXCL8和CXCL10 mRNA和蛋白质的上调,而在PTL中CCL8的上调。在以前通过免疫组织化学和图像分析评估的这些趋化因子和蜕膜白细胞丰度之间发现了显着的相关性。趋化因子主要由蜕膜基质细胞表达。此外,分娩期间母体血浆中的CXCL8和CCL5显着升高,表明趋化因子促成分娩期间的外周炎症事件。 TL和特发性PTL之间趋化因子表达模式的差异可能归因于在PTL中给予女性倍他米松抑制趋化因子表达。临床上相关浓度的类固醇可导致趋化因子下调的体外证据支持了这一点。本研究提供了令人信服的证据,表明趋化因子在分娩过程中调节蜕膜白细胞的募集。鉴定出的6种趋化因子代表了阻断PTL的潜在新治疗靶标。

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