Laboratório de Farmacologia, Instituto Butantan, São Paulo 05503-900, Brazil.
Instituto Clodomiro Picado, Facultad de Microbiología, Universidad de Costa Rica, San José 11501-2060, Costa Rica.
Biomolecules. 2020 Nov 24;10(12):1593. doi: 10.3390/biom10121593.
Adipose tissue secretes proinflammatory mediators which promote systemic and adipose tissue inflammation seen in obesity. Group IIA (GIIA)-secreted phospholipase A (sPLA) enzymes are found to be elevated in plasma and adipose tissue from obese patients and are active during inflammation, generating proinflammatory mediators, including prostaglandin E (PGE). PGE exerts anti-lipolytic actions and increases triacylglycerol levels in adipose tissue. However, the inflammatory actions of GIIA sPLAs in adipose tissue cells and mechanisms leading to increased PGE levels in these cells are unclear. This study investigates the ability of a representative GIIA sPLA, MT-III, to activate proinflammatory responses in preadipocytes, focusing on the biosynthesis of prostaglandins, adipocytokines and mechanisms involved in these effects. Our results showed that MT-III induced biosynthesis of PGE, PGI, MCP-1, IL-6 and gene expression of leptin and adiponectin in preadipocytes. The MT-III-induced PGE biosynthesis was dependent on cytosolic PLA (cPLA)-α, cyclooxygenases (COX)-1 and COX-2 pathways and regulated by a positive loop via the EP receptor. Moreover, MT-III upregulated COX-2 and microsomal prostaglandin synthase (mPGES)-1 protein expression. MCP-1 biosynthesis induced by MT-III was dependent on the EP4 receptor, while IL-6 biosynthesis was dependent on EP3 receptor engagement by PGE. These data highlight preadipocytes as targets for GIIA sPLAs and provide insight into the roles played by this group of sPLAs in obesity.
脂肪组织分泌促炎介质,促进肥胖患者体内和脂肪组织的系统性和脂肪组织炎症。研究发现,ⅡA 组(GIIA)分泌型磷脂酶 A(sPLA)酶在肥胖患者的血浆和脂肪组织中升高,并在炎症期间活跃,产生促炎介质,包括前列腺素 E(PGE)。PGE 发挥抗脂解作用,并增加脂肪组织中的三酰基甘油水平。然而,GIIA sPLA 在脂肪组织细胞中的炎症作用以及导致这些细胞中 PGE 水平升高的机制尚不清楚。本研究调查了代表性的 GIIA sPLA,MT-III,在脂肪前体细胞中激活促炎反应的能力,重点研究前列腺素、脂肪细胞因子的生物合成以及这些作用涉及的机制。我们的结果表明,MT-III 诱导脂肪前体细胞中 PGE、PGI、MCP-1、IL-6 和瘦素和脂联素基因表达的生物合成。MT-III 诱导的 PGE 生物合成依赖于细胞质 PLA(cPLA)-α、环氧化酶(COX)-1 和 COX-2 途径,并通过 EP 受体的正反馈进行调节。此外,MT-III 上调 COX-2 和微粒体前列腺素合酶(mPGES)-1 蛋白表达。MT-III 诱导的 MCP-1 生物合成依赖于 EP4 受体,而 IL-6 生物合成依赖于 PGE 对 EP3 受体的结合。这些数据强调了脂肪前体细胞是 GIIA sPLA 的靶标,并深入了解了这群 sPLA 在肥胖中的作用。