Phosphodiesterase 3B (PDE3B) regulates NLRP3 inflammasome in adipose tissue

www.nature.com/scientificreports OPEN received: 05 March 2016 accepted: 31 May 2016 Published: 20 June 2016 Phosphodiesterase 3B (PDE3B) regulates NLRP3 inflammasome in adipose tissue Faiyaz Ahmad1,*, Youn Wook Chung1,*, Yan Tang1, Steven C Hockman1, Shiwei Liu1, Yusuf Khan1, Kevin Huo1, Eric Billings2, Marcelo J Amar1, Alan T Remaley1 & Vincent C Manganiello1 Activation of inflammation in white adipose tissue (WAT), includes infiltration/expansion of WAT macrophages, contributes pathogenesis of obesity, insulin resistance, and metabolic syndrome. The inflammasome comprises an intracellular sensor (NLR), caspase-1 and the adaptor ASC. Inflammasome activation leads to maturation of caspase-1 and processing of IL1β, contributing to many metabolic disorders and directing adipocytes to a more insulin-resistant phenotype. Ablation of PDE3B in WAT prevents inflammasome activation by reducing expression of NLRP3, caspase-1, ASC, AIM2, TNFα, IL1β and proinflammatory genes. Following IP injection of lipopolysaccharide (LPS), serum levels of IL1β and TNFα were reduced in PDE3B−/−mice compared to WT. Activation of signaling cascades, which mediate inflammasome responses, were modulated in PDE3B−/−mice WAT, including smad, NFAT, NFkB, and MAP kinases. Moreover, expression of chemokine CCL2, MCP-1 and its receptor CCR2, which play an important role in macrophage chemotaxis, were reduced in WAT of PDE3B−/−mice. In addition, atherosclerotic plaque formation was significantly reduced in the aorta of apoE−/−/PDE3B−/−and LDLR−/−/PDE3B−/−mice compared to apoE−/−and LDL-R−/−mice, respectively. Obesity-induced changes in serum-cholesterol were blocked in PDE3B−/−mice. Collectively, these data establish a role for PDE3B in modulating inflammatory response, which may contribute to a reduced inflammatory state in adipose tissue. Insulin resistance, arthritis, asthma and obesity are associated with systemic inflammation which is characterized by increased cytokine and chemokine production and activated inflammasomes1,2. Similarly, fasting reduces inflammation in overweight adults. Adipose tissue macrophages (ATMs), and a wide variety of immune cells including T cells, B-cells and monocytes, infiltrate adipose tissue and increase the production of pro-inflammatory cytokines which play important roles in the contribution of adipose tissue to the development of obesity and insulin resistance3. Release of inflammatory mediators from adipocytes may also contribute to inflammation4. Increased fat mass associated with obesity leads to enlargement of adipose tissue. Crosstalk among enlarged adipocytes (which are less responsive to insulin), macrophages, and activated endothelial cells perpetuate a vicious cycle of macrophage infiltration mediated by monocyte chemoattractant protein (MCP-1) and aggravate the inflammatory state5,6. The NLRP3 inflammasome, a reactive oxygen species-sensitive and oxidized mtDNA (mitochondrial DNA)-bound multi-protein complex, regulates IL-1βmaturation and provides the protein scaffolds required to activate proinflammatory pathways through caspase-1 activation2,6,7. Mitochondrial dysfunction and generation of reactive oxygen species are implicated in cellular stress, leading to activation of NLRP3 inflammasome and insulin resistance8. The assembly of the NLRP3 inflammasome involves the interaction of pyrin domains of NLRP3 and ASC [apoptosis-associated, speck-like protein containing a C-terminal CARD (Caspase Activation Recruitment Domain)], and CARD-CARD interactions of ASC with procaspase-17. The adipose tissue macrophages (ATMs) can be classified into M1 pro-inflammatory classically activated macrophages and M2 anti-inflammatory macrophages3,9 . In adipose tissue, the NLRP3 inflammasome promotes classical M1 macrophage activation, leading 1 Cardiovascular and Pulmonary Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA. 2The laboratory of Computational Biology, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA. ∗These authors contributed equally to this work. Correspondence and requests for materials should be addressed to F.A. (email: ) Scientific Reports | 6:28056 | DOI: 10.1038/srep28056 1 www.nature.com/scientificreports/ to inflammation and metabolic diseases9,10. Mice lacking key genes of the inflammasome, such as ASC, NLRP3, and caspase-1, are defective in maturation and secretion of IL1βand IL1811, and are protected from adipocyte hypertrophy, hyperinsulinemia, high-fat diet weight gain, and obesity-induced insulin resistance4,6,7. Mice with reduced expression of NLRP3 are protected from diet-induced insulin resistance, correlating with the reduced activation of T cells in adipose tissue. Loss of TNFαor IL-1βor treatment with caspase-1 inhibitor also substantially improves insulin sensitivity4,12. Consistent with these data, studies in clinical trials have shown that IL1βsignaling blockade using anakinra (recombinant human IL1 receptor antagonist) leads to improvement in type-2 diabetes (T2D) and inflammation13. In human studies, treatment of T2D individuals with thiazolidinediones (insulin-sensitizers), reduced ATMs and inflammatory factors, and improved insulin resistance14. An anti-diabetic drug (sulfonylurea glyburide) has been shown to act as an inhibitor of NLRP315, suggesting that NLRP3 inflammasome may be a promising therapeutic target in T2D clinical trials. Thus, WAT contributes not only to modulation of energy utilization and homeostasis, but also to metabolic dysregulation that characterizes insulin resistance and obesity-related metabolic and cardiovascular complications. The PDE superfamily contains 11 structurally-related and functionally distinct PDE gene families (PDEs 1-11)16. The PDE3 family includes PDE3A and PDE3B, which are generated from two similarly organized genes, hydrolyze cAMP and cGMP, and are specifically inhibited by milrinone, cilostamide and cilostazol16. In general, PDE3B isoforms are relatively more highly expressed than PDE3A in tissues that regulate energy homeostasis, including adipose tissue, liver, and pancreatic β cells16,17. In adipocytes, insulin-induced activation of PDE3B mediates some acute metabolic actions of insulin, including inhibition of hormone-sensitive lipase and, thereby, hydrolysis of stored triglycerides16,17. Increased cAMP/ protein kinase A signaling is most likely responsible for reduced expression of proinflammatory genes18 and PKA-mediated suppression of NF-κB plays a role in controlling peripheral T lymphocytes, important in inflammation19. cAMP binding to NLRP3 promotes its ubiquitination and degradation20,21. However, the impact of long-term alteration of PDE3B expression on regulation of NLRP3 inflammasome and PDE3B regulation of insulin sensitivity remains to be determined. Here we show that targeted inactivation of the murine PDE3B gene resulted in decreased activation of the NLRP3 in (...truncated)