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The role and regulation of the nuclear factor kappa B signalling pathway in human labour.

机译:核因子κB信号转导通路在人工中的作用和调控。

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Within the discipline of reproductive biology, our understanding of one of the most fundamental biological processes is lacking--the cellular and molecular mechanisms that govern birth. This lack of understanding limits our ability to reduce the incidence of labour complications. The incidence of labour complications including: preterm labour; cervical incompetence; and post-date pregnancies has not diminished in decades. The key to improving the management of human labour and delivery is an understanding of how the multiple processes that are requisite for a successful labour and delivery are coordinated to achieve a timely birth. Processes of human labour include the formation of: contraction associated proteins; inflammatory mediators (e.g. cytokines); uterotonic phospholipid metabolites (e.g. prostaglandins); and the induction of extracellular matrix (ECM) remodelling. Increasingly, it is becoming evident that labour onset and birth are the result of cross-talk between multiple components of an integrated network. This hypothesis is supported by recent data implicating various upstream regulatory pathways in the control of key labour-associated processes, including the activity of enzymes involved in the formation of prostaglandins and extracellular matrix remodelling, and mediators of inflammation. Clearly, the biochemical pathways involved in the formation of these mediators represent potential sites for intervention that may translate to therapeutic interventions to delay or prevent preterm labour and delivery. Available data strongly implicate the nuclear factor-kappaB (NF-kappaB) family as candidate upstream regulators of multiple labour-associated processes. Not only do these data warrant further detailed analysis of the involvement of these pathways in the process of human labour but also promise new insights into the key mechanisms that trigger birth and the identification of new therapeutic interventions that will improve the management of labour.
机译:在生殖生物学的学科中,我们对最基本的生物学过程之一的了解缺乏-控制出生的细胞和分子机制。这种缺乏了解限制了我们减少劳动并发症发生率的能力。劳动并发症的发生率包括:早产;宫颈功能不全数十年来,怀孕后的人数并没有减少。改善人工和分娩管理的关键是了解如何协调成功的人工和分娩所需的多个过程以实现及时分娩。人类劳动的过程包括形成:收缩相关蛋白;炎性介质(例如细胞因子);子宫内膜磷脂代谢产物(例如前列腺素);以及诱导细胞外基质(ECM)重塑。越来越明显的是,分娩和分娩是集成网络中多个组件之间相互影响的结果。最新的数据支持这一假设,这些数据涉及关键劳工相关过程的控制中的各种上游调节途径,包括参与前列腺素和细胞外基质重塑的酶的活性以及炎症介质。显然,参与这些介体形成的生化途径代表了潜在的干预部位,可能转化为治疗性干预措施,以延迟或预防早产和分娩。现有数据强烈暗示了核因子-κB(NF-kappaB)家族是与多种劳工相关的过程的候选上游调节剂。这些数据不仅需要进一步详细分析这些途径在人类劳动过程中的参与,而且还有望对触发出生的关键机制有新的认识,并有望确定新的治疗措施,以改善劳动管理。

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