| Literature DB >> 31991095 |
Myungsun Shin1, Timothy B Ware1, Ku-Lung Hsu2.
Abstract
Here, we apply quantitative chemical proteomics and untargeted lipidomics to assign a polyunsaturated fatty acid (PUFA)-specific triacylglycerol (TAG) lipase activity for diacylglycerol lipase-beta (DAGLβ) in macrophages. We demonstrate that DAGLβ but not DAGLα is expressed and active in bone marrow-derived macrophages (BMDMs) as determined by activity-based protein profiling analysis of SILAC BMDMs. Genetic disruption of DAGLβ resulted in accumulation of cellular TAGs composed of PUFA but not saturated/low unsaturated fatty acid counterparts, which is recapitulated in wild-type macrophages treated with a DAGLβ-selective inhibitor. Biochemical assays with synthetic substrates confirm PUFA-TAGs as authentic DAGLβ substrates. In summary, our findings identify DAGLβ as a PUFA-specific TAG lipase in primary macrophages.Entities:
Keywords: 2-arachidonoylglycerol; TAG lipase; activity-based protein profiling; adipose triglyceride; chemical proteomics; diacylglycerol; diacylglycerol lipase; endocannabinoid; inflammation; lipidomics; lipolysis; macrophage; triglyceride
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Year: 2020 PMID: 31991095 PMCID: PMC7093258 DOI: 10.1016/j.chembiol.2020.01.005
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116