Hypoxia drives murine neutrophil protein scavenging to maintain central carbon metabolism
Watts, Emily R. and Howden, Andrew J.M. and Morrison, Tyler and Sadiku, Pranvera and Hukelmann, Jens and von Kriegsheim, Alex and Ghesquiere, Bart and Murphy, Fiona and Mirchandani, Ananda S. and Humphries, Duncan C. and Grecian, Robert and Ryan, Eilise M. and Coelho, Patricia and Blanco, Gio Rodriguez and Plant, Tracie M. and Dickinson, Rebecca S. and Finch, Andy and Vermaelen, Wesley and Cantrell, Doreen A. and Whyte, Moira K. and Walmsley, Sarah R. (2021) Hypoxia drives murine neutrophil protein scavenging to maintain central carbon metabolism. Journal of Clinical Investigation, 131 (10). e134073. ISSN 0021-9738 (https://doi.org/10.1172/JCI134073)
Preview |
Text.
Filename: Watts_etal_JCI_2021_Hypoxia_drives_murine_neutrophil_protein_scavenging.pdf
Final Published Version License: Download (1MB)| Preview |
Abstract
Limiting dysfunctional neutrophilic inflammation while preserving effective immunity requires a better understanding of the processes that dictate neutrophil function in the tissues. Quantitative mass-spectrometry identified how inflammatory murine neutrophils regulated expression of cell surface receptors, signal transduction networks, and metabolic machinery to shape neutrophil phenotypes in response to hypoxia. Through the tracing of labeled amino acids into metabolic enzymes, proinflammatory mediators, and granule proteins, we demonstrated that ongoing protein synthesis shapes the neutrophil proteome. To maintain energy supplies in the tissues, neutrophils consumed extracellular proteins to fuel central carbon metabolism. The physiological stresses of hypoxia and hypoglycemia, characteristic of inflamed tissues, promoted this extracellular protein scavenging with activation of the lysosomal compartment, further driving exploitation of the protein-rich inflammatory milieu. This study provides a comprehensive map of neutrophil proteomes, analysis of which has led to the identification of active catabolic and anabolic pathways that enable neutrophils to sustain synthetic and effector functions in the tissues.
ORCID iDs
Watts, Emily R., Howden, Andrew J.M., Morrison, Tyler, Sadiku, Pranvera, Hukelmann, Jens, von Kriegsheim, Alex, Ghesquiere, Bart, Murphy, Fiona ORCID: https://orcid.org/0000-0001-7925-0632, Mirchandani, Ananda S., Humphries, Duncan C., Grecian, Robert, Ryan, Eilise M., Coelho, Patricia, Blanco, Gio Rodriguez, Plant, Tracie M., Dickinson, Rebecca S., Finch, Andy, Vermaelen, Wesley, Cantrell, Doreen A., Whyte, Moira K. and Walmsley, Sarah R.;-
-
Item type: Article ID code: 86501 Dates: DateEvent17 May 2021Published6 April 2021Published Online31 March 2021AcceptedSubjects: Science > Natural history > Biology
Medicine > Medicine (General)Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 16 Aug 2023 14:17 Last modified: 11 Nov 2024 14:01 URI: https://strathprints.strath.ac.uk/id/eprint/86501