| Literature DB >> 33519814 |
Xiangyun Li1,2, Nathanial K Berg1, Tingting Mills3, Kaiying Zhang1, Holger K Eltzschig1, Xiaoyi Yuan1.
Abstract
Hypoxia and inflammation often coincide in pathogenic conditions such as acute respiratory distress syndrome (ARDS) and chronic lung diseases, which are significant contributors to morbidity and mortality for the general population. For example, the recent global outbreak of Coronavirus disease 2019 (COVID-19) has placed viral infection-induced ARDS under the spotlight. Moreover, chronic lung disease ranks the third leading cause of death in the United States. Hypoxia signaling plays a diverse role in both acute and chronic lung inflammation, which could partially be explained by the divergent function of downstream target pathways such as adenosine signaling. Particularly, hypoxia signaling activates adenosine signaling to inhibit the inflammatory response in ARDS, while in chronic lung diseases, it promotes inflammation and tissue injury. In this review, we discuss the role of adenosine at the interphase of hypoxia and inflammation in ARDS and chronic lung diseases, as well as the current strategy for therapeutic targeting of the adenosine signaling pathway.Entities:
Keywords: acute lung injury; adenosine; chronic lung injury; hypoxia; hypoxia-inducible factor; inflammation
Year: 2021 PMID: 33519814 PMCID: PMC7840604 DOI: 10.3389/fimmu.2020.604944
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561