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[해외논문] Angiopoietin-2 blockade ameliorates autoimmune neuroinflammation by inhibiting leukocyte recruitment into the CNS 원문보기

The Journal of clinical investigation, v.130 no.4, 2020년, pp.1977 - 1990  

Li, Zhilin (Wihuri Research Institute and Translational Cancer Medicine Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.) ,  Korhonen, Emilia A. (Wihuri Research Institute and Translational Cancer Medicine Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.) ,  Merlini, Arianna (Institute for Neuroimmunology and Multiple Sclerosis Research, University Medical Centre Gö) ,  Strauss, Judith (ttingen, Gö) ,  Wihuri, Eleonoora (ttingen, Germany.) ,  Nurmi, Harri (Institute for Neuroimmunology and Multiple Sclerosis Research, University Medical Centre Gö) ,  Antila, Salli (ttingen, Gö) ,  Paech, Jennifer (ttingen, Germany.) ,  Deutsch, Urban (Wihuri Research Institute and Translational Cancer Medicine Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.) ,  Engelhardt, Britta (Wihuri Research Institute and Translational Cancer Medicine Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.) ,  Chintharlapalli, Sudhakar (Wihuri Research Institute and Translational Cancer Medicine Program, Faculty of Medicine, University of Helsinki, Helsinki, Finland.) ,  Koh, Gou Young (Wihuri Research Institute and Translational Cancer Medicine P) ,  Flügel, Alexander ,  Alitalo, Kari

Abstract AI-Helper 아이콘AI-Helper

Angiopoietin-2 (Ang2), a ligand of the endothelial Tie2 tyrosine kinase, is involved in vascular inflammation and leakage in critically ill patients. However, the role of Ang2 in demyelinating central nervous system (CNS) autoimmune diseases is unknown. Here, we report that Ang2 is critically involv...

참고문헌 (66)

  1. 1 Abbott NJ Patabendige AA Dolman DE Yusof SR Begley DJ Structure and function of the blood-brain barrier Neurobiol Dis 2010 37 1 13 25 10.1016/j.nbd.2009.07.030 19664713 

  2. 2 Larochelle C Alvarez JI Prat A How do immune cells overcome the blood-brain barrier in multiple sclerosis? FEBS Lett 2011 585 23 3770 3780 10.1016/j.febslet.2011.04.066 21550344 

  3. 3 Constantinescu CS Farooqi N O’Brien K Gran B Experimental autoimmune encephalomyelitis (EAE) as a model for multiple sclerosis (MS) Br J Pharmacol 2011 164 4 1079 1106 10.1111/j.1476-5381.2011.01302.x 21371012 

  4. 4 Saharinen P Eklund L Alitalo K Therapeutic targeting of the angiopoietin-TIE pathway Nat Rev Drug Discov 2017 16 9 635 661 10.1038/nrd.2016.278 28529319 

  5. 5 Parikh SM Angiopoietins and Tie2 in vascular inflammation Curr Opin Hematol 2017 24 5 432 438 10.1097/MOH.0000000000000361 28582314 

  6. 6 Yuan HT Khankin EV Karumanchi SA Parikh SM Angiopoietin 2 is a partial agonist/antagonist of Tie2 signaling in the endothelium Mol Cell Biol 2009 29 8 2011 2022 10.1128/MCB.01472-08 19223473 

  7. 7 Korhonen EA et al Tie1 controls angiopoietin function in vascular remodeling and inflammation J Clin Invest 2016 126 9 3495 3510 10.1172/JCI84923 27548530 

  8. 8 Augustin HG Koh GY Thurston G Alitalo K Control of vascular morphogenesis and homeostasis through the angiopoietin-Tie system Nat Rev Mol Cell Biol 2009 10 3 165 177 19234476 

  9. 9 Thurston G et al Angiopoietin-1 protects the adult vasculature against plasma leakage Nat Med 2000 6 4 460 463 10.1038/74725 10742156 

  10. 10 Gurnik S et al Angiopoietin-2-induced blood-brain barrier compromise and increased stroke size are rescued by VE-PTP-dependent restoration of Tie2 signaling Acta Neuropathol 2016 131 5 753 773 10.1007/s00401-016-1551-3 26932603 

  11. 11 Lee SJ et al Angiopoietin-2 exacerbates cardiac hypoxia and inflammation after myocardial infarction J Clin Invest 2018 128 11 5018 5033 10.1172/JCI99659 30295643 

  12. 12 Ghosh CC et al Drug repurposing screen identifies Foxo1-dependent angiopoietin-2 regulation in sepsis Crit Care Med 2015 43 7 e230 e240 10.1097/CCM.0000000000000993 25855898 

  13. 13 Fiedler U et al Angiopoietin-2 sensitizes endothelial cells to TNF-alpha and has a crucial role in the induction of inflammation Nat Med 2006 12 2 235 239 10.1038/nm1351 16462802 

  14. 14 Hakanpaa L et al Targeting β1-integrin inhibits vascular leakage in endotoxemia Proc Natl Acad Sci U S A 2018 115 28 E6467 E6476 10.1073/pnas.1722317115 29941602 

  15. 15 Benest AV et al Angiopoietin-2 is critical for cytokine-induced vascular leakage PLoS One 2013 8 8 e70459 10.1371/journal.pone.0070459 23940579 

  16. 16 Han S et al Amelioration of sepsis by TIE2 activation-induced vascular protection Sci Transl Med 2016 8 335 335ra55 10.1126/scitranslmed.aad9260 27099174 

  17. 17 Holopainen T et al Effects of angiopoietin-2-blocking antibody on endothelial cell-cell junctions and lung metastasis J Natl Cancer Inst 2012 104 6 461 475 10.1093/jnci/djs009 22343031 

  18. 18 Schmittnaegel M et al Dual angiopoietin-2 and VEGFA inhibition elicits antitumor immunity that is enhanced by PD-1 checkpoint blockade Sci Transl Med 2017 9 385 eaak9670 10.1126/scitranslmed.aak9670 28404865 

  19. 19 Li Z Ma L Kulesskaya N Voikar V Tian L Microglia are polarized to M1 type in high-anxiety inbred mice in response to lipopolysaccharide challenge Brain Behav Immun 2014 38 237 248 10.1016/j.bbi.2014.02.008 24561490 

  20. 20 Nathan C Cunningham-Bussel A Beyond oxidative stress: an immunologist’s guide to reactive oxygen species Nat Rev Immunol 2013 13 5 349 361 10.1038/nri3423 23618831 

  21. 21 Krasemann S et al The TREM2-APOE pathway drives the transcriptional phenotype of dysfunctional microglia in neurodegenerative diseases Immunity 2017 47 3 566 581.e9 10.1016/j.immuni.2017.08.008 28930663 

  22. 22 Hakanpaa L et al Endothelial destabilization by angiopoietin-2 via integrin β1 activation Nat Commun 2015 6 5962 25635707 

  23. 23 Nishizaka T Shi Q Sheetz MP Position-dependent linkages of fibronectin- integrin-cytoskeleton Proc Natl Acad Sci U S A 2000 97 2 692 697 10.1073/pnas.97.2.692 10639141 

  24. 24 Kirk SL Karlik SJ VEGF and vascular changes in chronic neuroinflammation J Autoimmun 2003 21 4 353 363 10.1016/S0896-8411(03)00139-2 14624758 

  25. 25 Tabruyn SP et al Angiopoietin-2-driven vascular remodeling in airway inflammation Am J Pathol 2010 177 6 3233 3243 10.2353/ajpath.2010.100059 20952594 

  26. 26 Fuxe J et al Angiopoietin/Tie2 signaling transforms capillaries into venules primed for leukocyte trafficking in airway inflammation Am J Pathol 2010 176 4 2009 2018 10.2353/ajpath.2010.090976 20133818 

  27. 27 Vanlandewijck M et al A molecular atlas of cell types and zonation in the brain vasculature Nature 2018 554 7693 475 480 10.1038/nature25739 29443965 

  28. 28 Sabbagh MF et al Transcriptional and epigenomic landscapes of CNS and non-CNS vascular endothelial cells Elife 2018 7 e36187 30188322 

  29. 29 Sorriento D Santulli G Del Giudice C Anastasio A Trimarco B Iaccarino G Endothelial cells are able to synthesize and release catecholamines both in vitro and in vivo Hypertension 2012 60 1 129 136 10.1161/HYPERTENSIONAHA.111.189605 22665130 

  30. 30 Cavallero S Shen H Yi C Lien CL Kumar SR Sucov HM CXCL12 signaling is essential for maturation of the ventricular coronary endothelial plexus and establishment of functional coronary circulation Dev Cell 2015 33 4 469 477 10.1016/j.devcel.2015.03.018 26017771 

  31. 31 Turesson C Endothelial expression of MHC class II molecules in autoimmune disease Curr Pharm Des 2004 10 2 129 143 10.2174/1381612043453414 14754393 

  32. 32 Pober JS Merola J Liu R Manes TD Antigen presentation by vascular cells Front Immunol 2017 8 1907 29312357 

  33. 33 Park JS et al Normalization of tumor vessels by Tie2 activation and Ang2 inhibition enhances drug delivery and produces a favorable tumor microenvironment Cancer Cell 2016 30 6 953 967 10.1016/j.ccell.2016.10.018 27960088 

  34. 34 Fiedler U Augustin HG Angiopoietins: a link between angiogenesis and inflammation Trends Immunol 2006 27 12 552 558 10.1016/j.it.2006.10.004 17045842 

  35. 35 Kim M et al Opposing actions of angiopoietin-2 on Tie2 signaling and FOXO1 activation J Clin Invest 2016 126 9 3511 3525 10.1172/JCI84871 27548529 

  36. 36 Fiedler U et al The Tie-2 ligand angiopoietin-2 is stored in and rapidly released upon stimulation from endothelial cell Weibel-Palade bodies Blood 2004 103 11 4150 4156 10.1182/blood-2003-10-3685 14976056 

  37. 37 Karampoor S Zahednasab H Ramagopalan S Mehrpour M Keyvani H Angiogenic factors are associated with multiple sclerosis J Neuroimmunol 2016 301 88 93 10.1016/j.jneuroim.2016.11.005 27887749 

  38. 38 Chaitanya GV et al Inflammation induces neuro-lymphatic protein expression in multiple sclerosis brain neurovasculature J Neuroinflammation 2013 10 125 24124909 

  39. 39 De Palma M Jain RK CD4 + T cell activation and vascular normalization: two sides of the same coin? Immunity 2017 46 5 773 775 10.1016/j.immuni.2017.04.015 28514684 

  40. 40 Raivich G Banati R Brain microglia and blood-derived macrophages: molecular profiles and functional roles in multiple sclerosis and animal models of autoimmune demyelinating disease Brain Res Brain Res Rev 2004 46 3 261 281 10.1016/j.brainresrev.2004.06.006 15571769 

  41. 41 Bruck W et al Monocyte/macrophage differentiation in early multiple sclerosis lesions Ann Neurol 1995 38 5 788 796 10.1002/ana.410380514 7486871 

  42. 42 Li H Cuzner ML Newcombe J Microglia-derived macrophages in early multiple sclerosis plaques Neuropathol Appl Neurobiol 1996 22 3 207 215 8804022 

  43. 43 McCombe PA de Jersey J Pender MP Inflammatory cells, microglia and MHC class II antigen-positive cells in the spinal cord of Lewis rats with acute and chronic relapsing experimental autoimmune encephalomyelitis J Neuroimmunol 1994 51 2 153 167 10.1016/0165-5728(94)90077-9 7910169 

  44. 44 Ajami B Bennett JL Krieger C McNagny KM Rossi FM Infiltrating monocytes trigger EAE progression, but do not contribute to the resident microglia pool Nat Neurosci 2011 14 9 1142 1149 10.1038/nn.2887 21804537 

  45. 45 Fang HY et al Hypoxia-inducible factors 1 and 2 are important transcriptional effectors in primary macrophages experiencing hypoxia Blood 2009 114 4 844 859 10.1182/blood-2008-12-195941 19454749 

  46. 46 Scholz A et al Angiopoietin-2 promotes myeloid cell infiltration in a β 2 -integrin-dependent manner Blood 2011 118 18 5050 5059 10.1182/blood-2011-03-343293 21868579 

  47. 47 Sinnathamby T Yun J Clavet-Lanthier ME Cheong C Sirois MG VEGF and angiopoietins promote inflammatory cell recruitment and mature blood vessel formation in murine sponge/Matrigel model J Cell Biochem 2015 116 1 45 57 10.1002/jcb.24941 25145474 

  48. 48 Lemieux C Maliba R Favier J Theoret JF Merhi Y Sirois MG Angiopoietins can directly activate endothelial cells and neutrophils to promote proinflammatory responses Blood 2005 105 4 1523 1530 10.1182/blood-2004-09-3531 15498854 

  49. 49 Kim J et al Tie2 activation promotes choriocapillary regeneration for alleviating neovascular age-related macular degeneration Sci Adv 2019 5 2 eaau6732 10.1126/sciadv.aau6732 30788433 

  50. 50 Bruttger J et al Genetic cell ablation reveals clusters of local self-renewing microglia in the mammalian central nervous system Immunity 2015 43 1 92 106 10.1016/j.immuni.2015.06.012 26163371 

  51. 51 Russo MV Latour LL McGavern DB Distinct myeloid cell subsets promote meningeal remodeling and vascular repair after mild traumatic brain injury Nat Immunol 2018 19 5 442 452 10.1038/s41590-018-0086-2 29662169 

  52. 52 Kuchroo VK Martin CA Greer JM Ju ST Sobel RA Dorf ME Cytokines and adhesion molecules contribute to the ability of myelin proteolipid protein-specific T cell clones to mediate experimental allergic encephalomyelitis J Immunol 1993 151 8 4371 4382 7691946 

  53. 53 Petersen MA Ryu JK Akassoglou K Fibrinogen in neurological diseases: mechanisms, imaging and therapeutics Nat Rev Neurosci 2018 19 5 283 301 10.1038/nrn.2018.13 29618808 

  54. 54 Ryu JK et al Fibrin-targeting immunotherapy protects against neuroinflammation and neurodegeneration Nat Immunol 2018 19 11 1212 1223 10.1038/s41590-018-0232-x 30323343 

  55. 55 Jiang H Zhang F Yang J Han S Angiopoietin-1 ameliorates inflammation-induced vascular leakage and improves functional impairment in a rat model of acute experimental autoimmune encephalomyelitis Exp Neurol 2014 261 245 257 10.1016/j.expneurol.2014.05.013 24852101 

  56. 56 Sun JF et al Microvascular patterning is controlled by fine-tuning the Akt signal Proc Natl Acad Sci U S A 2005 102 1 128 133 10.1073/pnas.0403198102 15611473 

  57. 57 Stromnes IM Goverman JM Active induction of experimental allergic encephalomyelitis Nat Protoc 2006 1 4 1810 1819 10.1038/nprot.2006.285 17487163 

  58. 58 Flach AC et al Autoantibody-boosted T-cell reactivation in the target organ triggers manifestation of autoimmune CNS disease Proc Natl Acad Sci U S A 2016 113 12 3323 3328 10.1073/pnas.1519608113 26957602 

  59. 59 Schlager C Litke T Flugel A Odoardi F In vivo visualization of (auto)immune processes in the central nervous system of rodents Methods Mol Biol 2016 1304 117 129 25549830 

  60. 60 Warnick RE Fike JR Chan PH Anderson DK Ross GY Gutin PH Measurement of vascular permeability in spinal cord using Evans Blue spectrophotometry and correction for turbidity J Neurosci Methods 1995 58 1-2 167 171 10.1016/0165-0270(94)00172-D 7475223 

  61. 61 Georgiadou M et al AMPK negatively regulates tensin-dependent integrin activity J Cell Biol 2017 216 4 1107 1121 10.1083/jcb.201609066 28289092 

  62. 62 Lilja J et al SHANK proteins limit integrin activation by directly interacting with Rap1 and R-Ras Nat Cell Biol 2017 19 4 292 305 10.1038/ncb3487 28263956 

  63. 63 Butler A Hoffman P Smibert P Papalexi E Satija R Integrating single-cell transcriptomic data across different conditions, technologies, and species Nat Biotechnol 2018 36 5 411 420 10.1038/nbt.4096 29608179 

  64. 64 Huang da W Sherman BT Lempicki RA Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources Nat Protoc 2009 4 1 44 57 10.1038/nprot.2008.211 19131956 

  65. 65 Huang da W Sherman BT Lempicki RA Bioinformatics enrichment tools: paths toward the comprehensive functional analysis of large gene lists Nucleic Acids Res 2009 37 1 1 13 10.1093/nar/gkn923 19033363 

  66. 66 Zudaire E Gambardella L Kurcz C Vermeren S A computational tool for quantitative analysis of vascular networks PLoS One 2011 6 11 e27385 10.1371/journal.pone.0027385 22110636 

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