Evolution of the macrophage CD163 phenotype and cytokine profiles in a human model of resolving inflammation

International Journal of Inflammation

Volumn 2013, Issue , 2013, Pages

  Evans, Betsy J ^a   Haskard, Dorian O ^a   Sempowksi, Gregory ^b   Landis, R Clive ^c  

^a IMPERIAL COLLEGE LONDON   (United Kingdom)

^b DUKE UNIVERSITY MEDICAL CENTER   (United States)

^c UNIVERSITY OF THE WEST INDIES   (Jamaica)

Author keywords

[No Author keywords available]

Indexed keywords

CD14 ANTIGEN; CD163 ANTIGEN; CHEMOKINE; CYTOKINE; EOTAXIN; GAMMA INTERFERON INDUCIBLE PROTEIN 10; INTERLEUKIN 6; INTERLEUKIN 8; MACROPHAGE DERIVED CHEMOKINE; MACROPHAGE INFLAMMATORY PROTEIN 1ALPHA; MACROPHAGE INFLAMMATORY PROTEIN 1BETA; MONOCYTE CHEMOTACTIC PROTEIN 1; TUMOR NECROSIS FACTOR ALPHA;

ACUTE DISEASE; APOPTOSIS; ARTICLE; ASPIRATION; BLISTER; CELL INFILTRATION; CELL LINEAGE; CONTROLLED STUDY; DERMATITIS; DISEASE COURSE; DISEASE MODEL; FOREARM; HUMAN; HUMAN CELL; LEUKOCYTE; MACROPHAGE; MACROPHAGE FUNCTION; MOLECULAR EVOLUTION; MONOCYTE; NEUTROPHIL; PHAGOCYTOSIS; PHENOTYPE; PRIORITY JOURNAL; UPREGULATION; WOUND HEALING;

EID: 84877971572     PISSN: 20908040     EISSN: 20420099     Source Type: Journal    
DOI: 10.1155/2013/780502     Document Type: Article

References (45)

1. Gillitzer R., Goebeler M., Chemokines in cutaneous wound healing. Journal of Leukocyte Biology 2001 69 4 513 521 2-s2.0-0035075706 (Pubitemid 32294835)
2. Barrientos S., Stojadinovic O., Golinko M. S., Brem H., Tomic-Canic M., Growth factors and cytokines in wound healing. Wound Repair and Regeneration 2008 16 5 585 601 2-s2.0-51349167276 10.1111/j.1524-475X.2008.00410.x
3. Leibovich S. J., Ross R., The role of the macrophage in wound repair: a study with hydrocortisone and antimacrophage serum. American Journal of Pathology 1975 78 1 71 99 2-s2.0-0016428338
4. Low Q. E. H., Drugea I. A., Duffner L. A., Quinn D. G., Cook D. N., Rollins B. J., Kovacs E. J., DiPietro L. A., Wound healing in MIP-1 α -/- and MCP-1-/- mice. American Journal of Pathology 2001 159 2 457 463 2-s2.0-0034888877 (Pubitemid 32751076)
5. Stout R. D., Editorial: macrophage functional phenotypes: no alternatives in dermal wound healing? Journal of Leukocyte Biology 2010 87 1 19 21 2-s2.0-74949124402 10.1189/jlb.0509311
6. Dijkstra C. D., Dopp E. A., Joling P., Kraal G., The heterogeneity of mononuclear phagocytes in lymphoid organs: distinct macrophage subpopulations in the rat recognized by monoclonal antibodies ED1, ED2 and ED3. Immunology 1985 54 3 589 599 2-s2.0-0021969667 (Pubitemid 15132717)
7. Zwadlo G., Voegeli R., Schulze Osthoff K., Sorg C., A monoclonal antibody to a novel differentiation antigen on human macrophages associated with the down-regulatory phase of the inflammatory process. Experimental Cell Biology 1987 55 6 295 304 2-s2.0-0023576184 (Pubitemid 18087127)
8. Gilroy D. W., Colville-Nash P. R., McMaster S., Sawatzky D. A., Willoughby D. A., Lawrence T., Inducible cyclooxygenase-derived 15-deoxyΔ12-14PGJ 2 brings about acute inflammatory resolution in rat pleurisy by inducing neutrophil and macrophage apoptosis. FASEB Journal 2003 17 15 2269 2271 2-s2.0-0642364442 10.1096/fj.02-1162fje (Pubitemid 39561462)
9. Yagnik D. R., Evans B. J., Florey O., Mason J. C., Landis R. C., Haskard D. O., Macrophage release of transforming growth factor β 1 during resolution of monosodium urate monohydrate crystal-induced inflammation. Arthritis and Rheumatism 2004 50 7 2273 2280 2-s2.0-3142738734 10.1002/art.20317 (Pubitemid 38924406)
10. Boyle J. J., Harrington H. A., Piper E., Elderfield K., Stark J., Landis R. C., Haskard D. O., Coronary intraplaque hemorrhage evokes a novel atheroprotective macrophage phenotype. American Journal of Pathology 2009 174 3 1097 1108 2-s2.0-62549114844 10.2353/ajpath.2009.080431
11. Finn A. V., Nakano M., Polavarapu R., Karmali V., Saeed O., Zhao X., Yazdani S., Otsuka F., Davis T., Habib A., Narula J., Kolodgie F. D., Virmani R., Hemoglobin directs macrophage differentiation and prevents foam cell formation in human atherosclerotic plaques. Journal of the American College of Cardiology 2012 59 2 166 177
12. Boyle J. J., Heme and haemoglobin direct macrophage Mhem phenotype and counter foam cell formation in areas of intraplaque haemorrhage. Current Opinion in Lipidology 2012 23 5 453 461
13. Engelhardt E., Toksoy A., Goebeler M., Debus S., Bröcker E. B., Gillitzer R., Chemokines IL-8, GRO α MCP-1, IP-10, and mig are sequentially and differentially expressed during phase-specific infiltration of leukocyte subsets in human wound healing. American Journal of Pathology 1998 153 6 1849 1860 2-s2.0-0031740262 (Pubitemid 28550672)
14. Fahey T. J., Sherry B., Tracey K. J., van Deventer S., Jones W. G., Minei J. P., Morgello S., Shires G. T., Cerami A., Cytokine production in a model of wound healing: the appearance of MIP-1, MIP-2, cachectin/TNF and IL-I. Cytokine 1990 2 2 92 99 2-s2.0-0025400674
15. DiPietro L. A., Reintjes M. G., Low Q. E. H., Levi B., Gamelli R. L., Modulation of macrophage recruitment into wounds by monocyte chemoattractant protein-1. Wound Repair and Regeneration 2001 9 1 28 33 2-s2.0-0035065711 10.1046/j.1524-475X.2001.00028.x (Pubitemid 32268511)
16. Heinrich S. A., Messingham K. A. N., Gregory M. S., Colantoni A., Ferreira A. M., Dipietro L. A., Kovacs E. J., Elevated monocyte chemoattractant protein-1 levels following thermal injury precede monocyte recruitment to the wound site and are controlled, in part, by tumor necrosis factor- α Wound Repair and Regeneration 2003 11 2 110 119 2-s2.0-0037367203 10.1046/j.1524-475X. 2003.11206.x (Pubitemid 36514822)
17. DiPietro L. A., Burdick M., Low Q. E., Kunkel S. L., Strieter R. M., Mip-1 α as a critical macrophage chemoattractant in murine wound repair. Journal of Clinical Investigation 1998 101 8 1693 1698 2-s2.0-0032521671 (Pubitemid 28198499)
18. Honkanen R. E., Cantharidin, another natural toxin that inhibits the activity of serine/threonine protein phosphatases types 1 and 2A. FEBS Letters 1993 330 3 283 286 2-s2.0-0027217027 10.1016/0014-5793(93)80889-3 (Pubitemid 23276340)
19. Pierard-Franchimont C., Pierard G. E., Cantharidin-induced acantholysis. American Journal of Dermatopathology 1988 10 5 419 423 2-s2.0-0023711828
20. Tromovitch T. A., Cantharadin. Journal of the American Medical Association 1971 215 4 640 2-s2.0-0015238942 10.1001/jama.215.4.640
21. Day R. M., Harbord M., Forbes A., Segal A. W., Cantharidin blisters: a technique for investigating leukocyte trafficking and cytokine production at sites of inflammation in humans. Journal of Immunological Methods 2001 257 1-2 213 220 2-s2.0-0035515930
22. Ivetic T. V., Hrvacic B., Bosnar M., Cuzic S., Bosnjak B., Erakovic H. V., Glojnaric I., Cantharidin-induced inflammation in mouse ear model for translational research of novel anti-inflammatories. Translational Research 2012 160 2 137 145
23. Evans B. J., McDowall A., Taylor P. C., Hogg N., Haskard D. O., Landis R. C., Shedding of lymphocyte function-associated antigen-1 (LFA-1) in a human inflammatory response. Blood 2006 107 9 3593 3599 2-s2.0-33646431420 10.1182/blood-2005-09-3695
24. Dransfield I., Buckle A. M., Savill J. S., McDowall A., Haslett C., Hogg N., Neutrophil apoptosis is associated with a reduction in CD16 (Fc γ RIII) expression. Journal of Immunology 1994 153 3 1254 1263 2-s2.0-0028245643 (Pubitemid 24228517)
25. Martinez F. O., Sica A., Mantovani A., Locati M., Macrophage activation and polarization. Frontiers in Bioscience 2008 13 2 453 461 2-s2.0-38449102676 10.2741/2692 (Pubitemid 351599757)
26. Hübner G., Brauchle M., Smola H., Madlener M., Fässler R., Werner S., Differential regulation of pro-inflammatory cytokines during wound healing in normal and glucocorticoid-treated mice. Cytokine 1996 8 7 548 556 2-s2.0-0030198562 10.1006/cyto.1996.0074 (Pubitemid 26294545)
27. Morris T., Stables M., Colville-Nash P., Newson J., Bellingan G., De Souza P. M., Gilroy D. W., Dichotomy in duration and severity of acute inflammatory responses in humans arising from differentially expressed proresolution pathways. Proceedings of the National Academy of Sciences of the United States of America 2010 107 19 8842 8847 2-s2.0-77952725991 10.1073/pnas.1000373107
28. Tyler L. W., Matossian K., Todd R., Gallagher G. T., White R. R., Wong D. T. W., Eosinophil-derived transforming growth factors (TGF- α and TGF- β 1) in human periradicular lesions. Journal of Endodontics 1999 25 9 619 624 2-s2.0-0033182101
29. Wong D. T. W., Donoff R. B., Yang J., Song B. Z., Matossian K., Nagura N., Elovic A., McBride J., Gallagher G., Todd R., Chiang T., Chou L. S. S., Chou Ming Yung, Galli S. J., Weller P. F., Sequential expression of transforming growth factors α and β 1 by eosinophils during cutaneous wound healing in the hamster. American Journal of Pathology 1993 143 1 130 142 2-s2.0-23444431975 (Pubitemid 24058167)
30. Harbord M. W. N., Marks D. J. B., Forbes A., Bloom S. L., Day R. M., Segal A. W., Impaired neutrophil chemotaxis in Crohn's disease relates to reduced production of chemokines and can be augmented by granulocyte-colony stimulating factor. Alimentary Pharmacology and Therapeutics 2006 24 4 651 660 2-s2.0-33746469061 10.1111/j.1365-2036.2006.03016.x (Pubitemid 44127847)
31. Hayashida K., Parks W. C., Pyong W. P., Syndecan-1 shedding facilitates the resolution of neutrophilic inflammation by removing sequestered CXC chemokines. Blood 2009 114 14 3033 3043 2-s2.0-70449468813 10.1182/blood-2009- 02-204966
32. Angus McQuibban G., Gong J. H., Wong J. P., Wallace J. L., Clark-Lewis I., Overall C. M., Matrix metalloproteinase processing of monocyte chemoattractant proteins generates CC chemokine receptor antagonists with anti-inflammatory properties in vivo. Blood 2002 100 4 1160 1167 2-s2.0-0037103183 (Pubitemid 34864266)
33. Mortier A., Van D. J., Proost P., Overview of the mechanisms regulating chemokine activity and availability. Immunology Letters 2012 145 1-2 2 9
34. Cromack D. T., Sporn M. B., Roberts A. B., Merino M. J., Dart L. L., Norton J. A., Transforming growth factor β levels in rat wound chambers. Journal of Surgical Research 1987 42 6 622 628 2-s2.0-0023250784 (Pubitemid 17103651)
35. Siqueira M. F., Li J., Chehab L., Desta T., Chino T., Krothpali N., Behl Y., Alikhani M., Yang J., Braasch C., Graves D. T., Impaired wound healing in mouse models of diabetes is mediated by TNF- α dysregulation and associated with enhanced activation of forkhead box O1 (FOXO1). Diabetologia 2010 53 2 378 388 2-s2.0-77949310647 10.1007/s00125-009-1529-y
36. Goren I., Müller E., Pfeilschifter J., Frank S., Severely impaired insulin signaling in chronic wounds of diabetic ob/ob mice: a potential role of tumor necrosis factor- α American Journal of Pathology 2006 168 3 765 777 2-s2.0-33644651282 10.2353/ajpath.2006.050293 (Pubitemid 43327729)
37. Gretzer C., Emanuelsson L., Liljensten E., Thomsen P., The inflammatory cell influx and cytokines changes during transition from acute inflammation to fibrous repair around implanted materials. Journal of Biomaterials Science, Polymer Edition 2006 17 6 669 687 2-s2.0-33746078519 10.1163/156856206777346340 (Pubitemid 44069701)
38. Buechler C., Ritter M., Orsó E., Langmann T., Klucken J., Schmitz G., Regulation of scavenger receptor CD163 expression in human monocytes and macrophages by pro- and antiinflammatory stimuli. Journal of Leukocyte Biology 2000 67 1 97 103 2-s2.0-0001930725 (Pubitemid 30046823)
39. Daley J. M., Brancato S. K., Thomay A. A., Reichner J. S., Albina J. E., The phenotype of murine wound macrophages. Journal of Leukocyte Biology 2010 87 1 59 67 2-s2.0-74949115952 10.1189/jlb.0409236
40. Philippidis P., Mason J. C., Evans B. J., Nadra I., Taylor K. M., Haskard D. O., Landis R. C., Hemoglobin scavenger receptor CD163 mediates interleukin-10 release and heme oxygenase-1 synthesis: antiinflammatory monocyte-macrophage responses in vitro, in resolving skin blisters in vivo, and after cardiopulmonary bypass surgery. Circulation Research 2004 94 1 119 126 2-s2.0-0347951196 10.1161/01.RES.0000109414.78907.F9 (Pubitemid 38064106)
41. Schaer D. J., Alayash A. I., Clearance and control mechanisms of hemoglobin from cradle to grave. Antioxidants and Redox Signaling 2010 12 2 181 184 2-s2.0-77949507206 10.1089/ars.2009.2923
42. Boyle J. J., Johns M., Kampfer T., Nguyen A. T., Game L., Schaer D. J., Mason J. C., Haskard D. O., Activating transcription factor 1 directs Mhem atheroprotective macrophages through coordinated iron handling and foam cell protection. Circulation Research 2012 110 1 20 33
43. Boyle J. J., Johns M., Lo J., Chiodini A., Ambrose N., Evans P. C., Mason J. C., Haskard D. O., Heme induces heme oxygenase 1 via Nrf2: role in the homeostatic macrophage response to intraplaque hemorrhage. Arteriosclerosis, Thrombosis, and Vascular Biology 2011 31 11 2685 2691
44. Evans B. J., Haskard D. O., Finch J. R., Hambleton I. R., Landis R. C., Taylor K. M., The inflammatory effect of cardiopulmonary bypass on leukocyte extravasation in vivo. Journal of Thoracic and Cardiovascular Surgery 2008 135 5 999 1006 2-s2.0-42949174653 10.1016/j.jtcvs.2007.08.071 (Pubitemid 351609033)
45. Buckley C. D., Gilroy D. W., Serhan C. N., Stockinger B., Tak P. P., The resolution of inflammation. Nature Reviews Immunology 2013 13 1 59 66