Regulation of glycolytic genes in human macrophages by oxysterols: a potential role for liver X receptors

Subset of macrophages within the atheroma plaque displays a high glucose uptake activity. Nevertheless, the molecular mechanisms and the pathophysiological significance of this high glucose need remain unclear. While the role for hypoxia and hypoxia inducible factor 1α has been demonstrated, the contribution of lipid micro‐environment and more specifically oxysterols is yet to be explored.

[1]  J. Pais de Barros,et al.  Interplay between Liver X Receptor and Hypoxia Inducible Factor 1α Potentiates Interleukin-1β Production in Human Macrophages. , 2020, Cell reports.

[2]  Matthew S. Tremblay,et al.  Cell-specific discrimination of desmosterol and desmosterol mimetics confers selective regulation of LXR and SREBP in macrophages , 2018, Proceedings of the National Academy of Sciences.

[3]  Steve Alexander,et al.  Experimental design and analysis and their reporting II: updated and simplified guidance for authors and peer reviewers , 2018, British journal of pharmacology.

[4]  J. Adamski,et al.  Altered metabolism distinguishes high-risk from stable carotid atherosclerotic plaques , 2018, European heart journal.

[5]  Christopher H George,et al.  Goals and practicalities of immunoblotting and immunohistochemistry: A guide for submission to the British Journal of Pharmacology , 2018, British journal of pharmacology.

[6]  P. Libby,et al.  Antiinflammatory Therapy with Canakinumab for Atherosclerotic Disease , 2017, The New England journal of medicine.

[7]  G. Litjens,et al.  In-depth tissue profiling using multiplexed immunohistochemical consecutive staining on single slide , 2016, Science Immunology.

[8]  S. Giorgetti-Peraldi,et al.  Disruption of Glut1 in Hematopoietic Stem Cells Prevents Myelopoiesis and Enhanced Glucose Flux in Atheromatous Plaques of ApoE(-/-) Mice. , 2016, Circulation research.

[9]  K. Bornfeldt,et al.  Macrophage Phenotype and Function in Different Stages of Atherosclerosis. , 2016, Circulation research.

[10]  P. Libby,et al.  Moderate Hypoxia Potentiates Interleukin-1&bgr; Production in Activated Human Macrophages , 2014, Circulation research.

[11]  T. Nishizawa,et al.  Testing the role of myeloid cell glucose flux in inflammation and atherosclerosis. , 2014, Cell reports.

[12]  Liang Zheng,et al.  Succinate is an inflammatory signal that induces IL-1β through HIF-1α , 2013, Nature.

[13]  S. Haas,et al.  Genome-wide analysis of LXRα activation reveals new transcriptional networks in human atherosclerotic foam cells , 2013, Nucleic acids research.

[14]  G. Poli,et al.  Plaque oxysterols induce unbalanced up-regulation of matrix metalloproteinase-9 in macrophagic cells through redox-sensitive signaling pathways: Implications regarding the vulnerability of atherosclerotic lesions. , 2011, Free radical biology & medicine.

[15]  P. Libby,et al.  Hypoxia but not inflammation augments glucose uptake in human macrophages: Implications for imaging atherosclerosis with 18fluorine-labeled 2-deoxy-D-glucose positron emission tomography. , 2011, Journal of the American College of Cardiology.

[16]  Christophe Ladroue,et al.  Comparative Lipidomics Profiling of Human Atherosclerotic Plaques , 2011, Circulation. Cardiovascular genetics.

[17]  M-O Lee,et al.  27 POSITIVE CROSS-TALK BETWEEN HYPOXIA INDUCIBLE FACTOR-1α AND LIVER X RECEPTOR α INDUCES FORMATION OF TRIGLYCERIDE-LOADED FOAM CELLS , 2011 .

[18]  Michael R. Elliott,et al.  Identification of a Novel Macrophage Phenotype That Develops in Response to Atherogenic Phospholipids via Nrf2 , 2010, Circulation research.

[19]  C. Glass,et al.  Macrophages, oxysterols and atherosclerosis. , 2010, Circulation journal : official journal of the Japanese Circulation Society.

[20]  Paul R Reid,et al.  Discovery of tertiary sulfonamides as potent liver X receptor antagonists. , 2010, Journal of medicinal chemistry.

[21]  Annie Costa,et al.  Induction of Transglutaminase 2 by a Liver X Receptor/Retinoic Acid Receptor &agr; Pathway Increases the Clearance of Apoptotic Cells by Human Macrophages , 2009, Circulation research.

[22]  D. Koller,et al.  The Immunological Genome Project: networks of gene expression in immune cells , 2008, Nature Immunology.

[23]  Mathijs Groeneweg,et al.  Hypoxia, hypoxia-inducible transcription factor, and macrophages in human atherosclerotic plaques are correlated with intraplaque angiogenesis. , 2008, Journal of the American College of Cardiology.

[24]  Ahmed Tawakol,et al.  In vivo 18F-fluorodeoxyglucose positron emission tomography imaging provides a noninvasive measure of carotid plaque inflammation in patients. , 2006, Journal of the American College of Cardiology.

[25]  Wei Li,et al.  Oxysterol mixtures, in atheroma-relevant proportions, display synergistic and proapoptotic effects. , 2006, Free radical biology & medicine.

[26]  K. Højlund,et al.  Skeletal muscle lipid accumulation in type 2 diabetes may involve the liver X receptor pathway. , 2005, Diabetes.

[27]  L. Corcos,et al.  Comparison of the cytotoxic, pro-oxidant and pro-inflammatory characteristics of different oxysterols , 2005, Cell Biology and Toxicology.

[28]  A. Sandelin,et al.  Prediction of nuclear hormone receptor response elements. , 2005, Molecular endocrinology.

[29]  M. Hayashi,et al.  Induction of glucose transporter 1 expression through hypoxia-inducible factor 1alpha under hypoxic conditions in trophoblast-derived cells. , 2004, The Journal of endocrinology.

[30]  A. Sevanian,et al.  Oxysterol mixtures prevent proapoptotic effects of 7‐ ketocholesterol in macrophages: implications for proatherogenic gene modulation , 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[31]  A. Kuksis,et al.  Phospholipids and oxophospholipids in atherosclerotic plaques at different stages of plaque development , 2004, Lipids.

[32]  David E. Misek,et al.  Microarray Analyses during Adipogenesis: Understanding the Effects of Wnt Signaling on Adipogenesis and the Roles of Liver X Receptor α in Adipocyte Metabolism , 2002, Molecular and Cellular Biology.

[33]  J. Pickard,et al.  Imaging Atherosclerotic Plaque Inflammation With [18F]-Fluorodeoxyglucose Positron Emission Tomography , 2002, Circulation.

[34]  F. Guardiola,et al.  Oxysterol profiles of normal human arteries, fatty streaks and advanced lesions , 2001, Free radical research.

[35]  T. Hayek,et al.  Selective distribution of oxysterols in atherosclerotic lesions and human plasma lipoproteins , 2001, Free radical research.

[36]  Andrew J. Brown,et al.  Oxysterols and atherosclerosis. , 1999, Atherosclerosis.

[37]  R. Dean,et al.  7-Hydroperoxycholesterol and its products in oxidized low density lipoprotein and human atherosclerotic plaque. , 1997, Journal of lipid research.

[38]  V. Kostulas,et al.  Localization of sterol 27-hydroxylase immuno-reactivity in human atherosclerotic plaques. , 1997, Biochimica et biophysica acta.

[39]  D. Mangelsdorf,et al.  An oxysterol signalling pathway mediated by the nuclear receptor LXRα , 1996, Nature.

[40]  C. van der Veen,et al.  Lipids and oxidised lipids in human atherosclerotic lesions at different stages of development. , 1995, Biochimica et biophysica acta.

[41]  Olive Lloyd-Baker IDENTIFICATION OF NOVEL , 1964 .

[42]  Christian Schmidl,et al.  Genome-wide identification of hypoxia-inducible factor-1 and -2 binding sites in hypoxic human macrophages alternatively activated by IL-10. , 2015, Biochimica et biophysica acta.

[43]  B. Demirel,et al.  Respiratory epithelial adenomatoid hamartoma (REAH) of the nasopharynx with high 18F-FDG uptake on PET/CT. , 2014, B-ENT.

[44]  F. Guardiola,et al.  Oxysterols in cap and core of human advanced atherosclerotic lesions. , 1999, Free radical research.