A novel mechanism for polyunsaturated fatty acid uptake and action in neutrophils

NIH RePORTER · NIH · R01 · $689,666 · view on reporter.nih.gov ↗

Abstract

Project Summary / Abstract: Neutrophils are a major type of leukocytes that play important roles in acute inflammation. They are typically the first leukocytes to be recruited to inflammatory sites and can eliminate pathogens by multiple mechanisms, including releasing neutrophil extracellular traps (NETs). Although neutrophils are important for normal immune responses, particularly to microbial infections, they are also responsible for and/or contribute to many inflammatory diseases, including myocardial ischemia-reperfusion injury (MIRI). In our preliminary studies, we found that neutrophil-specific KO of LRP5 (Lrp5N) aggravates heart injury in the MIRI model by enhancing neutrophil activation. Our preliminary results further indicate that LRP5 may function as a transporter for polyunsaturated fatty acids (PUFAs) and is required for PUFA-mediated inhibition of mTORC1 signaling in neutrophils. In this application, we plan to determine how LRP5 transports PUFAs and how important LRP5- transported PUFAs are for the regulation of neutrophil activities and inflammation diseases related to neutrophils, including MIRI.

Key facts

NIH application ID
10976584
Project number
1R01HL171071-01A1
Recipient
YALE UNIVERSITY
Principal Investigator
Dianqing Wu
Activity code
R01
Funding institute
NIH
Fiscal year
2024
Award amount
$689,666
Award type
1
Project period
2024-07-01 → 2028-04-30