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Article ; Online: Identification of oxidative stress and Toll-like receptor 4 signaling as a key pathway of acute lung injury.

Imai, Yumiko / Kuba, Keiji / Neely, G Greg / Yaghubian-Malhami, Rubina / Perkmann, Thomas / van Loo, Geert / Ermolaeva, Maria / Veldhuizen, Ruud / Leung, Y H Connie / Wang, Hongliang / Liu, Haolin / Sun, Yang / Pasparakis, Manolis / Kopf, Manfred / Mech, Christin / Bavari, Sina / Peiris, J S Malik / Slutsky, Arthur S / Akira, Shizuo /
Hultqvist, Malin / Holmdahl, Rikard / Nicholls, John / Jiang, Chengyu / Binder, Christoph J / Penninger, Josef M

Cell

2008  Volume 133, Issue 2, Page(s) 235–249

Abstract: ... to acute respiratory distress syndrome. Here we report that Toll-like receptor 4 (TLR4) mutant mice display ... natural resistance to acid-induced acute lung injury (ALI). We show that TLR4-TRIF-TRAF6 signaling is a key disease ... improves the severity of H5N1-mediated ALI. Our data identify oxidative stress and innate immunity as key ...

Abstract Multiple lung pathogens such as chemical agents, H5N1 avian flu, or SARS cause high lethality due to acute respiratory distress syndrome. Here we report that Toll-like receptor 4 (TLR4) mutant mice display natural resistance to acid-induced acute lung injury (ALI). We show that TLR4-TRIF-TRAF6 signaling is a key disease pathway that controls the severity of ALI. The oxidized phospholipid (OxPL) OxPAPC was identified to induce lung injury and cytokine production by lung macrophages via TLR4-TRIF. We observed OxPL production in the lungs of humans and animals infected with SARS, Anthrax, or H5N1. Pulmonary challenge with an inactivated H5N1 avian influenza virus rapidly induces ALI and OxPL formation in mice. Loss of TLR4 or TRIF expression protects mice from H5N1-induced ALI. Moreover, deletion of ncf1, which controls ROS production, improves the severity of H5N1-mediated ALI. Our data identify oxidative stress and innate immunity as key lung injury pathways that control the severity of ALI.
MeSH term(s) Adaptor Proteins, Vesicular Transport/metabolism ; Animals ; Humans ; Influenza, Human/metabolism ; Interleukin-6/metabolism ; Lung ; Mice ; Mice, Inbred C57BL ; NADPH Oxidases/metabolism ; NF-kappa B/metabolism ; Orthomyxoviridae Infections/metabolism ; Oxidative Stress ; Phospholipids/metabolism ; Respiratory Distress Syndrome/metabolism ; Severe Acute Respiratory Syndrome/metabolism ; Signal Transduction ; Toll-Like Receptor 4/metabolism
Chemical Substances Adaptor Proteins, Vesicular Transport ; Interleukin-6 ; NF-kappa B ; Phospholipids ; Toll-Like Receptor 4 ; NADPH Oxidases (EC 1.6.3.-)
Keywords covid19
Language English
Publishing date 2008-04-16
Publishing country United States
Document type Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 187009-9
ISSN 1097-4172 ; 0092-8674
ISSN (online) 1097-4172
ISSN 0092-8674
DOI 10.1016/j.cell.2008.02.043
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Zs.A 1167: Show issues Location:
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