This is a R01 project to study the role of Phospholipase D4 (PLD4) in nucleic acid sensing. Leukocytes carry conserved sensors for endocytosed DNA and RNA that trigger the production of proinflammatory cytokines, including type I interferon. The ensuing inflammation can be beneficial for host defense to microorganisms, viruses, and tumors, but can also be pathogenic, and may thwart the use of potentially therapeutic oligonucleotides. PLD4 is a lysosomal protein whose function is not understood. Genome-wide association studies have linked PLD4 to human rheumatoid arthritis and systemic sclerosis. We find that PLD4-deficient mice have a phenotype similar to the human disease macrophage activation syndrome, which is mimicked in mice by repeated injections with Toll-like receptor 9 agonists. Here we test the hypotheses that PLD4 breaks down ingested DNA and RNA and regulates host defense and inflammation by promoting the destruction nucleic acids and regulating recognition by TLR7, TLR8 (in humans) and TLR9. We will characterize how PLD4 deficiency promotes a MAS-like phenotype and how deficiencies in PLD4 or PLD3+PLD4 affect TLR7 and TLR9 responses to specific ligands, leading to altered cytokine secretion. The possible role of PLD4 in self/nonself discrimination will also be assessed. The long-term goal of these studies is to understand the basic biology of PLD4, its functions in host defense and inflammation, and to develop a basis for potential future translational research.
Rheumatological diseases such as Rheumatoid Arthritis, Systemic Sclerosis and Alzheimer's disease often involve inflammation in response to DNA and RNA released from cells or microbes. PLD4 is a protein that we recently implicated in this response. Here we investigate how PLD4 interacts with DNA and RNA and how it affects inflammation.
