缺氧诱导的肠道信号传导和肝脏病理生物学。

IF 28.4 1区 医学 Q1 PATHOLOGY
Sumeet Solanki, Yatrik M Shah
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引用次数: 0

摘要

氧气(O2)对细胞代谢和生物化学反应至关重要。当氧气的需求超过供应时,就会发生缺氧。缺氧诱导因子(HIFs)对激活缺氧应激后的适应性和生存反应至关重要。在肠道和肝脏中,氧气梯度或生理性缺氧是维持正常稳态所必需的。虽然生理性缺氧是有益的,有助于正常功能,但病理性缺氧是有害的,因为它会加剧炎症反应和组织功能障碍,是许多癌症的标志。在这篇综述中,我们讨论了肠道和肝脏缺氧诱导的信号传导,主要集中在HIFs,在肠道和肝脏疾病的生理学和病理生物学中的作用。此外,我们还检测了HIFs在肠道和肝脏疾病期间各种细胞类型中的功能,而不仅仅是肠上皮和肝细胞HIFs。这篇综述强调了理解缺氧诱导的信号在肠道和肝脏疾病发病机制中的重要性,并强调了HIFs作为治疗靶点的潜力。《病理学年度评论:疾病机制》第19卷预计最终在线出版日期为2024年1月。请参阅http://www.annualreviews.org/page/journal/pubdates用于修订估算。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hypoxia-Induced Signaling in Gut and Liver Pathobiology.

Oxygen (O2) is essential for cellular metabolism and biochemical reactions. When the demand for O2 exceeds the supply, hypoxia occurs. Hypoxia-inducible factors (HIFs) are essential to activate adaptive and survival responses following hypoxic stress. In the gut (intestines) and liver, the presence of oxygen gradients or physiologic hypoxia is necessary to maintain normal homeostasis. While physiologic hypoxia is beneficial and aids in normal functions, pathological hypoxia is harmful as it exacerbates inflammatory responses and tissue dysfunction and is a hallmark of many cancers. In this review, we discuss the role of gut and liver hypoxia-induced signaling, primarily focusing on HIFs, in the physiology and pathobiology of gut and liver diseases. Additionally, we examine the function of HIFs in various cell types during gut and liver diseases, beyond intestinal epithelial and hepatocyte HIFs. This review highlights the importance of understanding hypoxia-induced signaling in the pathogenesis of gut and liver diseases and emphasizes the potential of HIFs as therapeutic targets.

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来源期刊
CiteScore
62.60
自引率
0.00%
发文量
40
期刊介绍: The Annual Review of Pathology: Mechanisms of Disease is a scholarly journal that has been published since 2006. Its primary focus is to provide a comprehensive overview of recent advancements in our knowledge of the causes and development of significant human diseases. The journal places particular emphasis on exploring the current and evolving concepts of disease pathogenesis, as well as the molecular genetic and morphological changes associated with various diseases. Additionally, the journal addresses the clinical significance of these findings. In order to increase accessibility and promote the broad dissemination of research, the current volume of the journal has transitioned from a gated subscription model to an open access format. This change has been made possible through the Annual Reviews' Subscribe to Open program, which allows all articles published in this volume to be freely accessible to readers. As part of this transition, all articles in the journal are published under a Creative Commons Attribution (CC BY) license, which encourages open sharing and use of the research.
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