| First Author | Watanabe K | Year | 2020 |
| Journal | J Biol Chem | Volume | 295 |
| Issue | 30 | Pages | 10092-10111 |
| PubMed ID | 32482892 | Mgi Jnum | J:301978 |
| Mgi Id | MGI:6466907 | Doi | 10.1074/jbc.RA120.013753 |
| Citation | Watanabe K, et al. (2020) Group V secreted phospholipase A2 plays a protective role against aortic dissection. J Biol Chem 295(30):10092-10111 |
| abstractText | Aortic dissection is a life-threatening aortopathy involving separation of the aortic wall, whose underlying mechanisms are still incompletely understood. Epidemiological evidence suggests that unsaturated fatty acids improve cardiovascular health. Here, using quantitative RT-PCR, histological analyses, magnetic cell sorting and flow cytometry assays, and MS-based lipidomics, we show that the activity of a lipid-metabolizing enzyme, secreted phospholipase A2 group V (sPLA2-V), protects against aortic dissection by endogenously mobilizing vasoprotective lipids. Global and endothelial cell-specific sPLA2-V-deficient mice frequently developed aortic dissection shortly after infusion of angiotensin II (AT-II). We observed that in the AT-II-treated aorta, endothelial sPLA2-V mobilized oleic and linoleic acids, which attenuated endoplasmic reticulum stress, increased the expression of lysyl oxidase, and thereby stabilized the extracellular matrix in the aorta. Of note, dietary supplementation with oleic or linoleic acid reversed the increased susceptibility of sPLA2-V-deficient mice to aortic dissection. These findings reveal an unexplored functional link between sPLA2-driven phospholipid metabolism and aortic stability, possibly contributing to the development of improved diagnostic and/or therapeutic strategies for preventing aortic dissection. |
