PLAAT1 deficiency alleviates high‐fat diet‐induced hepatic lipid accumulation in mice

Abstract

AbstractThe phospholipase A and acyltransferase (PLAAT) family is composed of three isoforms in mice (PLAAT1, 3, and 5), all of which function as phospholipid‐metabolizing enzymes exhibiting phospholipase A1/A2 and acyltransferase activities. Plaat3‐deficient (Plaat3−/−) mice were previously reported to show lean phenotype and remarkable hepatic fat accumulation under high‐fat diet (HFD) feeding, while Plaat1−/− mice have not been analyzed. In the present study, we generated Plaat1−/− mice and investigated the effects of PLAAT1 deficiency on HFD‐induced obesity, hepatic lipid accumulation, and insulin resistance. After HFD treatment, PLAAT1 deficiency caused a lower body weight gain compared to wild‐type mice. Plaat1−/− mice also showed reduced liver weight with negligible hepatic lipid accumulation. In accordance with these findings, PLAAT1 deficiency improved HFD‐induced hepatic dysfunction and lipid metabolism disorders. Lipidomics analysis in the liver revealed that in Plaat1−/− mice, the levels of various glycerophospholipids tended to increase, while all classes of lysophospholipids examined tended to decrease, suggesting that PLAAT1 functions as phospholipase A1/A2 in the liver. Interestingly, the HFD treatment of wild‐type mice significantly increased the mRNA level of PLAAT1 in the liver. Furthermore, the deficiency did not appear to elevate the risk of insulin resistance in contrast to PLAAT3 deficiency. These results suggested that the suppression of PLAAT1 improves HFD‐induced overweight and concomitant hepatic lipid accumulation.