CCAAT/Enhancer-binding Protein β (C/EBPβ) Expression Regulates Dietary-induced Inflammation in Macrophages and Adipose Tissue in Mice*
暂无分享,去创建一个
Mahua Choudhury | S. Rahman | J. Friedman | R. Janssen | M. Choudhury | Becky A de la Houssaye | Shaikh M Rahman | Rachel C Janssen | Karalee C Baquero | Rebecca M Aikens | Jacob E Friedman | B. A. de la Houssaye | Karalee C. Baquero
[1] M. Czaja,et al. Autophagy regulates adipose mass and differentiation in mice. , 2009, The Journal of clinical investigation.
[2] P. Sawchenko,et al. CCAAT/Enhancer Binding Protein-δ Expression by Dendritic Cells Regulates CNS Autoimmune Inflammatory Disease , 2011, The Journal of Neuroscience.
[3] Valeria Poli,et al. The Role of C/EBP Isoforms in the Control of Inflammatory and Native Immunity Functions* , 1998, The Journal of Biological Chemistry.
[4] Robert V Farese,et al. DGAT1-dependent triacylglycerol storage by macrophages protects mice from diet-induced insulin resistance and inflammation. , 2010, The Journal of clinical investigation.
[5] Peter Tontonoz,et al. LXR Signaling Couples Sterol Metabolism to Proliferation in the Acquired Immune Response , 2008, Cell.
[6] S. Gordon,et al. Monocyte and macrophage heterogeneity , 2005, Nature Reviews Immunology.
[7] D. Ramji,et al. CCAAT/enhancer-binding proteins: structure, function and regulation. , 2002, The Biochemical journal.
[8] U. Schibler,et al. A liver-enriched transcriptional activator protein, LAP, and a transcriptional inhibitory protein, LIP, are translated from the sam mRNA , 1991, Cell.
[9] D. Ron,et al. CHOP, a novel developmentally regulated nuclear protein that dimerizes with transcription factors C/EBP and LAP and functions as a dominant-negative inhibitor of gene transcription. , 1992, Genes & development.
[10] R. Eckel,et al. CCAAT/Enhancer-binding Protein β Deletion Reduces Adiposity, Hepatic Steatosis, and Diabetes in Leprdb/db Mice* , 2007, Journal of Biological Chemistry.
[11] J. Barrett,et al. CCAAT/enhancer binding protein α, β and δ gene variants: associations with obesity related phenotypes in the Leeds Family Study , 2010, Diabetes & vascular disease research.
[12] Jing Ye,et al. Up-Regulation of Mitochondrial Activity and Acquirement of Brown Adipose Tissue-Like Property in the White Adipose Tissue of Fsp27 Deficient Mice , 2008, PloS one.
[13] Vidya Subramanian,et al. Alternative M2 activation of Kupffer cells by PPARdelta ameliorates obesity-induced insulin resistance. , 2008, Cell metabolism.
[14] S. Tangye,et al. Inflammatory Mechanisms in Obesity , 2013 .
[15] D. Clegg,et al. Lipid-induced insulin resistance mediated by the proinflammatory receptor TLR4 requires saturated fatty acid-induced ceramide biosynthesis in mice. , 2011, The Journal of clinical investigation.
[16] P. Tontonoz,et al. Liver X receptors as integrators of metabolic and inflammatory signaling. , 2006, The Journal of clinical investigation.
[17] Y. Kido,et al. Ablation of C/EBPbeta alleviates ER stress and pancreatic beta cell failure through the GRP78 chaperone in mice. , 2010, The Journal of clinical investigation.
[18] K. Kristiansen,et al. Retinoblastoma protein functions as a molecular switch determining white versus brown adipocyte differentiation , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[19] Christopher K. Glass,et al. The peroxisome proliferator-activated receptor-γ is a negative regulator of macrophage activation , 1998, Nature.
[20] C. Dubois,et al. Inflammatory Cytokine Production by Human Neutrophils Involves C/EBP Transcription Factors1 , 2009, The Journal of Immunology.
[21] T. Graf,et al. Stepwise Reprogramming of B Cells into Macrophages , 2004, Cell.
[22] S. Rahman,et al. Fenofibrate and PBA prevent fatty acid-induced loss of adiponectin receptor and pAMPK in human hepatoma cells and in hepatitis C virus-induced steatosis , 2009, Journal of Lipid Research.
[23] I. Verma,et al. Hematopoietic cell-specific deletion of toll-like receptor 4 ameliorates hepatic and adipose tissue insulin resistance in high-fat-fed mice. , 2009, Cell metabolism.
[24] A. Smith,et al. Characterization of the Murine Fatty Acid Transport Protein Gene and Its Insulin Response Sequence* , 1998, The Journal of Biological Chemistry.
[25] Peter F. Johnson,et al. C5a-regulated CCAAT/Enhancer-binding Proteins β and δ Are Essential in Fcγ Receptor-mediated Inflammatory Cytokine and Chemokine Production in Macrophages* , 2011, The Journal of Biological Chemistry.
[26] S. Young,et al. Linking lipid metabolism to the innate immune response in macrophages through sterol regulatory element binding protein-1a. , 2011, Cell metabolism.
[27] YoshihiroOgawa,et al. Role of the Toll-like Receptor 4/NF-κB Pathway in Saturated Fatty Acid–Induced Inflammatory Changes in the Interaction Between Adipocytes and Macrophages , 2007 .
[28] Frank Brombacher,et al. Macrophage-specific PPARγ controls alternative activation and improves insulin resistance , 2007, Nature.
[29] K. Walsh,et al. Adiponectin Promotes Macrophage Polarization toward an Anti-inflammatory Phenotype* , 2009, The Journal of Biological Chemistry.
[30] M. Furuhashi,et al. Adipocyte/macrophage fatty acid-binding proteins contribute to metabolic deterioration through actions in both macrophages and adipocytes in mice. , 2008, The Journal of clinical investigation.
[31] W. Wahli,et al. Cyclooxygenase-2 Controls Energy Homeostasis in Mice by de Novo Recruitment of Brown Adipocytes , 2010, Science.
[32] M. Scadeng,et al. Bone marrow–specific Cap gene deletion protects against high-fat diet–induced insulin resistance , 2007, Nature Medicine.
[33] M. Fessler,et al. Toll-like receptor signaling links dietary fatty acids to the metabolic syndrome , 2009, Current opinion in lipidology.
[34] J. Olefsky,et al. Insulin sensitivity: modulation by nutrients and inflammation. , 2008, The Journal of clinical investigation.
[35] M. Lane,et al. Induction of fatty acid synthetase synthesis in differentiating 3T3-L1 preadipocytes. , 1980, The Journal of biological chemistry.
[36] S. Akira,et al. Differential Role for c-Rel and C/EBPβ/δ in TLR-Mediated Induction of Proinflammatory Cytokines1 , 2009, The Journal of Immunology.
[37] M. Tschöp,et al. PKCzeta-regulated inflammation in the nonhematopoietic compartment is critical for obesity-induced glucose intolerance. , 2010, Cell metabolism.
[38] Nathan R. Qi,et al. The Protein Kinase IKKɛ Regulates Energy Balance in Obese Mice , 2009, Cell.
[39] Katherine A. Fitzgerald,et al. Serum Amyloid A Activates the NLRP3 Inflammasome and Promotes Th17 Allergic Asthma in Mice , 2011, The Journal of Immunology.
[40] S. Akira,et al. Defective adipocyte differentiation in mice lacking the C/EBPβ and/or C/EBPδ gene , 1997 .
[41] C. Glass,et al. FoxO1 regulates Tlr4 inflammatory pathway signalling in macrophages , 2010, The EMBO journal.
[42] A. Saltiel,et al. Obesity induces a phenotypic switch in adipose tissue macrophage polarization. , 2007, The Journal of clinical investigation.
[43] K. Moore,et al. Atherogenic lipids and lipoproteins trigger CD36-TLR2-dependent apoptosis in macrophages undergoing endoplasmic reticulum stress. , 2010, Cell metabolism.
[44] J. Ntambi,et al. Cloning and characterization of the human stearoyl-CoA desaturase gene promoter: transcriptional activation by sterol regulatory element binding protein and repression by polyunsaturated fatty acids and cholesterol. , 2001, Biochemical and biophysical research communications.
[45] M. Karin,et al. JNK1 in hematopoietically derived cells contributes to diet-induced inflammation and insulin resistance without affecting obesity. , 2007, Cell metabolism.
[46] T. Graf,et al. Reprogramming of committed T cell progenitors to macrophages and dendritic cells by C/EBP alpha and PU.1 transcription factors. , 2006, Immunity.
[47] J. Friedman,et al. Increased Insulin Receptor Substrate-1 and Enhanced Skeletal Muscle Insulin Sensitivity in Mice Lacking CCAAT/Enhancer-binding Protein β* , 2000, The Journal of Biological Chemistry.
[48] K. Kim,et al. Roles of CCAAT/enhancer-binding protein and its binding site on repression and derepression of acetyl-CoA carboxylase gene. , 1994, The Journal of biological chemistry.
[49] A. Chervonsky,et al. Deletion of Fas in adipocytes relieves adipose tissue inflammation and hepatic manifestations of obesity in mice. , 2010, The Journal of clinical investigation.
[50] S. Yamaoka,et al. Role of the Toll-like Receptor 4/NF-&kgr;B Pathway in Saturated Fatty Acid–Induced Inflammatory Changes in the Interaction Between Adipocytes and Macrophages , 2007, Arteriosclerosis, thrombosis, and vascular biology.
[51] Carey N Lumeng,et al. Inflammatory links between obesity and metabolic disease. , 2011, The Journal of clinical investigation.
[52] W. Farrar,et al. Inhibition of adhesive interaction between multiple myeloma and bone marrow stromal cells by PPARgamma cross talk with NF-kappaB and C/EBP. , 2007, Blood.
[53] C. Kahn,et al. Increased P85α Is a Potent Negative Regulator of Skeletal Muscle Insulin Signaling and Induces in Vivo Insulin Resistance Associated with Growth Hormone Excess* , 2005, Journal of Biological Chemistry.
[54] A. Hevener,et al. IKK-β links inflammation to obesity-induced insulin resistance , 2005, Nature Medicine.
[55] S. Watkins,et al. Reducing endoplasmic reticulum stress through a macrophage lipid chaperone alleviates atherosclerosis , 2009, Nature Medicine.
[56] Sarah Hummasti,et al. Endoplasmic Reticulum Stress and Inflammation in Obesity and Diabetes , 2010, Circulation research.
[57] J. Flier,et al. TLR4 links innate immunity and fatty acid-induced insulin resistance. , 2006, The Journal of clinical investigation.
[58] Jill M. Schroeder-Gloeckler,et al. CCAAT/enhancing binding protein β deletion in mice attenuates inflammation, endoplasmic reticulum stress, and lipid accumulation in diet‐induced nonalcoholic steatohepatitis , 2007, Hepatology.
[59] C. Buechler,et al. Fatty acid‐induced induction of Toll‐like receptor‐4/nuclear factor‐κB pathway in adipocytes links nutritional signalling with innate immunity , 2009, Immunology.
[60] Tsonwin Hai,et al. Adipocyte CREB promotes insulin resistance in obesity. , 2009, Cell metabolism.