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缺氧。缺氧、缺氧诱导因子与髓系细胞功能。

Hypoxia. Hypoxia, hypoxia inducible factor and myeloid cell function.

作者信息

Walmsley Sarah R, Chilvers Edwin R, Whyte Moira K B

机构信息

Academic Unit of Respiratory Medicine, School of Medicine and Biomedical Sciences, University of Sheffield, Royal Hallamshire Hospital, Sheffield, UK.

出版信息

Arthritis Res Ther. 2009;11(2):219. doi: 10.1186/ar2632. Epub 2009 Apr 21.

Abstract

With little in the way of effective therapeutic strategies to target the innate immune response, a better understanding of the critical pathways regulating neutrophil and macrophage responses in inflammation is key to the development of novel therapies. Hypoxia inducible factor (HIF) was originally identified as a central transcriptional regulator of cellular responses to oxygen deprivation. However, the HIF signalling pathway now appears, in myeloid cells at least, to be a master regulator of both immune cell function and survival. As such, understanding the biology of HIF and its regulators may provide new approaches to myeloid-specific therapies that are urgently needed.

摘要

由于针对先天免疫反应几乎没有有效的治疗策略,更好地理解炎症中调节中性粒细胞和巨噬细胞反应的关键途径是开发新疗法的关键。缺氧诱导因子(HIF)最初被确定为细胞对缺氧反应的核心转录调节因子。然而,现在至少在髓系细胞中,HIF信号通路似乎是免疫细胞功能和存活的主要调节因子。因此,了解HIF及其调节因子的生物学特性可能为迫切需要的髓系特异性疗法提供新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e01e/2688173/3813675908a7/ar2632-1.jpg

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