Gartung Allison, Zhao Jiawei, Chen Simon, Mottillo Emilio, VanHecke Garrett C, Ahn Young-Hoon, Maddipati Krishna Rao, Sorokin Andrey, Granneman James, Lee Menq-Jer
From the Bioactive Lipid Research Program, Department of Pathology.
Department of Pathology.
J Biol Chem. 2016 Jul 29;291(31):16001-10. doi: 10.1074/jbc.M116.725937. Epub 2016 May 31.
Excessive adipocyte lipolysis generates lipid mediators and triggers inflammation in adipose tissue. However, the specific roles of lipolysis-generated mediators in adipose inflammation remain to be elucidated. In the present study, cultured 3T3-L1 adipocytes were treated with isoproterenol to activate lipolysis and the fatty acyl lipidome of released lipids was determined by using LC-MS/MS. We observed that β-adrenergic activation elevated levels of approximately fifty lipid species, including metabolites of cyclooxygenases, lipoxygenases, epoxygenases, and other sources. Moreover, we found that β-adrenergic activation induced cyclooxygenase 2 (COX-2), not COX-1, expression in a manner that depended on activation of hormone-sensitive lipase (HSL) in cultured adipocytes and in the epididymal white adipose tissue (EWAT) of C57BL/6 mice. We found that lipolysis activates the JNK/NFκB signaling pathway and inhibition of the JNK/NFκB axis abrogated the lipolysis-stimulated COX-2 expression. In addition, pharmacological inhibition of COX-2 activity diminished levels of COX-2 metabolites during lipolytic activation. Inhibition of COX-2 abrogated the induction of CCL2/MCP-1 expression by β-adrenergic activation and prevented recruitment of macrophage/monocyte to adipose tissue. Collectively, our data indicate that excessive adipocyte lipolysis activates the JNK/NFκB pathway leading to the up-regulation of COX-2 expression and recruitment of inflammatory macrophages.
过量的脂肪细胞脂解作用会产生脂质介质并引发脂肪组织炎症。然而,脂解产生的介质在脂肪炎症中的具体作用仍有待阐明。在本研究中,用异丙肾上腺素处理培养的3T3-L1脂肪细胞以激活脂解作用,并使用LC-MS/MS测定释放脂质的脂肪酰基脂质组。我们观察到β-肾上腺素能激活使约五十种脂质种类的水平升高,包括环氧化酶、脂氧合酶、环氧合酶和其他来源的代谢产物。此外,我们发现β-肾上腺素能激活以依赖于培养的脂肪细胞和C57BL/6小鼠附睾白色脂肪组织(EWAT)中激素敏感性脂肪酶(HSL)激活的方式诱导环氧化酶2(COX-2)而非COX-1的表达。我们发现脂解激活JNK/NFκB信号通路,抑制JNK/NFκB轴可消除脂解刺激的COX-2表达。此外,COX-2活性的药理学抑制降低了脂解激活期间COX-2代谢产物的水平。抑制COX-2可消除β-肾上腺素能激活诱导的CCL2/MCP-1表达,并阻止巨噬细胞/单核细胞向脂肪组织募集。总体而言,我们的数据表明过量的脂肪细胞脂解激活JNK/NFκB通路,导致COX-2表达上调和炎性巨噬细胞募集。