Innate immunity in the vasculature: Interactions with pathogenic bacteria

Current Opinion in Microbiology

Volumn 15, Issue 1, 2012, Pages 85-91

  Harding, Mark ^a   Kubes, Paul ^a  

^a UNIVERSITY OF CALGARY   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIGEN; BETA2 INTEGRIN; CD31 ANTIGEN; CD99 ANTIGEN; CHEMOKINE RECEPTOR; CYTOKINE; ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE 1; INTERCELLULAR ADHESION MOLECULE 1; INTERCELLULAR ADHESION MOLECULE 2; PADGEM PROTEIN; TOLL LIKE RECEPTOR; TOLL LIKE RECEPTOR 4; VASCULAR CELL ADHESION MOLECULE 1;

ADAPTIVE IMMUNITY; ANTIGEN PRESENTATION; BACTERIAL INFECTION; BACTERICIDAL ACTIVITY; BACTERIUM; CELLULAR IMMUNITY; CYTOKINE PRODUCTION; DENDRITIC CELL; ENDOTHELIUM CELL; ESCHERICHIA COLI; HOST PATHOGEN INTERACTION; HUMAN; INNATE IMMUNITY; INVARIANT NATURAL KILLER T CELL; KUPFFER CELL; LEUKOCYTE ADHERENCE; LEUKOCYTE MIGRATION; MACROPHAGE; MONOCYTE; NATURAL KILLER T CELL; NEUTROPHIL CHEMOTAXIS; NONHUMAN; PHAGOCYTOSIS; REVIEW; STAPHYLOCOCCUS AUREUS; STREPTOCOCCUS PYOGENES; THROMBOCYTE FUNCTION; VASCULAR ENDOTHELIUM; VASCULARIZATION;

ANIMALS; ANTIGEN PRESENTATION; BACTERIA; BLOOD PLATELETS; BLOOD VESSELS; ENDOTHELIAL CELLS; HOST-PATHOGEN INTERACTIONS; HUMANS; IMMUNITY, INNATE; KUPFFER CELLS; NEUTROPHILS; PHAGOCYTOSIS;

BACTERIA (MICROORGANISMS);

EID: 84856104734     PISSN: 13695274     EISSN: 18790364     Source Type: Journal    
DOI: 10.1016/j.mib.2011.11.010     Document Type: Review

References (54)

1. Hickey M.J., Kubes P. Intravascular immunity: the host-pathogen encounter in blood vessels. Nat Rev Immunol 2009, 9:364-375.
2. Sumagin R., Sarelius I.H. Intercellular adhesion molecule-1 enrichment near tricellular endothelial junctions is preferentially associated with leukocyte transmigration and signals for reorganization of these junctions to accommodate leukocyte passage. J Immunol 2010, 184:5242-5252.
3. Phillipson M., Kaur J., Colarusso P., Ballantyne C.M., Kubes P. Endothelial domes encapsulate adherent neutrophils and minimize increases in vascular permeability in paracellular and transcellular emigration. PLoS ONE 2008, 3:e1649.
4. Petri B., Phillipson M., Kubes P. The physiology of leukocyte recruitment: an in vivo perspective. J Immunol 2008, 180:6439-6446.
5. Nathan C. Neutrophils and immunity: challenges and opportunities. Nat Rev Immunol 2006, 6:173-182.
6. McDonald B., McAvoy E.F., Lam F., Gill V., de l.M., Savani R.C., Kubes P. Interaction of CD44 and hyaluronan is the dominant mechanism for neutrophil sequestration in inflamed liver sinusoids. J Exp Med 2008, 205:915-927.
7. Wang Q., Pfeiffer G.R., Stevens T., Doerschuk C.M. Lung microvascular and arterial endothelial cells differ in their responses to intercellular adhesion molecule-1 ligation. Am J Respir Crit Care Med 2002, 166:872-877.
8. Kuligowski M.P., Kitching A.R., Hickey M.J. Leukocyte recruitment to the inflamed glomerulus: a critical role for platelet-derived P-selectin in the absence of rolling. J Immunol 2006, 176:6991-6999.
9. Andonegui G., Zhou H., Bullard D., Kelly M.M., Mullaly S.C., McDonald B., Long E.M., Robbins S.M., Kubes P. Mice that exclusively express TLR4 on endothelial cells can efficiently clear a lethal systemic Gram-negative bacterial infection. J Clin Invest 2009, 119:1921-1930.
10. Ye X., Ding J., Zhou X., Chen G., Liu S.F. Divergent roles of endothelial NF-κB in multiple organ injury and bacterial clearance in mouse models of sepsis. J Exp Med 2008, 205:1303-1315.
11. Teijaro J., Walsh K., Cahalan S., Fremgen D., Roberts E., Scott F., Martinborough E., Peach R., Oldstone M.A., Rosen H. Endothelial cells are central orchestrators of cytokine amplification during influenza virus infection. Cell 2011, 146:980-991.
12. Lemichez E., Lecuit M., Nassif X., Bourdoulous S. Breaking the wall: targeting of the endothelium by pathogenic bacteria. Nat Rev Microbiol 2010, 8:93-104.
13. Sethi S., Herrmann M., Roller J., von Müller L., Peerschke E.I., Ghebrehiwet B., Bajric I., Menger M.D., Laschke M.W. Blockade of gC1qR/p33, a receptor for C1q, inhibits adherence of Staphylococcus aureus to the microvascular endothelium. Microvasc Res 2011, 82:66-72.
14. Doulet N., Donnadieu E., Laran-Chich M., Niedergang F., Nassif X., Couraud P.O., Bourdoulous S. Neisseria meningitidis infection of human endothelial cells interferes with leukocyte transmigration by preventing the formation of endothelial docking structures. J Cell Biol 2006, 173:627-637.
15. Ruiz-Perez F., Wahid R., Faherty C.S., Kolappaswamy K., Rodriguez L., Santiago A., Murphy E., Cross A., Sztein M.B., Nataro J.P. Serine protease autotransporters from Shigella flexneri and pathogenic Escherichia coli target a broad range of leukocyte glycoproteins. Proc Natl Acad Sci 2011, 108:12881-12886.
16. Lin A., Loughman J.A., Zinselmeyer B.H., Miller M.J., Caparon M.G. Streptolysin S inhibits neutrophil recruitment during the early stages of Streptococcus pyogenes infection. Infect Immun 2009, 77:5190-5201.
17. Datta V., Myskowski S.M., Kwinn L.A., Chiem D.N., Varki N., Kansal R.G., Kotb M., Nizet V. Mutational analysis of the group A streptococcal operon encoding streptolysin S and its virulence role in invasive infection. Mol Microbiol 2005, 56:681-695.
18. Brinkmann V., Reichard U., Goosmann C., Fauler B., Uhlemann Y., Weiss D.S., Weinrauch Y., Zychlinsky A. Neutrophil extracellular traps kill bacteria. Science 2004, 303:1532-1535.
19. Urban C.F., Ermert D., Schmid M., Abu-Abed U., Goosmann C., Nacken W., Brinkmann V., Jungblut P.R., Zychlinsky A. Neutrophil extracellular traps contain calprotectin, a cytosolic protein complex involved in host defense against Candida albicans. PLoS Pathog 2009, 5:e1000639.
20. Clark S.R., Ma A.C., Tavener S.A., McDonald B., Goodarzi Z., Kelly M.M., Patel K.D., Chakrabarti S., McAvoy E., Sinclair G.D., et al. Platelet TLR4 activates neutrophil extracellular traps to ensnare bacteria in septic blood. Nat Med 2007, 13:463-469.
21. Yousefi S., Mihalache C., Kozlowski E., Schmid I., Simon H.U. Viable neutrophils release mitochondrial DNA to form neutrophil extracellular traps. Cell Death Differ 2009, 16:1438-1444.
22. Pilsczek F.H., Salina D., Poon K.K.H., Fahey C., Yipp B.G., Sibley C.D., Robbins S.M., Green F.H.Y., Surette M.G., Sugai M., et al. A novel mechanism of rapid nuclear neutrophil extracellular trap formation in response to Staphylococcus aureus. J Immunol 2010, 185:7413-7425.
23. Fuchs T.A., Abed U., Goosmann C., Hurwitz R., Schulze I., Wahn V., Weinrauch Y., Brinkmann V., Zychlinsky A. Novel cell death program leads to neutrophil extracellular traps. J Cell Biol 2007, 176:231-241.
24. Fuchs T.A., Brill A., Duerschmied D., Schatzberg D., Monestier M., Myers D.D., Wrobleski S.K., Wakefield T.W., Hartwig J.H., Wagner D.D. Extracellular DNA traps promote thrombosis. Proc Natl Acad Sci 2010, 107:15880-15885.
25. Massberg S., Grahl L., von Bruehl M., Manukyan D., Pfeiler S., Goosmann C., Brinkmann V., Lorenz M., Bidzhekov K., Khandagale A.B., et al. Reciprocal coupling of coagulation and innate immunity via neutrophil serine proteases. Nat Med 2010, 16:887-896.
26. Buchanan J.T., Simpson A.J., Aziz R.K., Liu G.Y., Kristian S.A., Kotb M., Feramisco J., Nizet V. DNase expression allows the pathogen group A Streptococcus to escape killing in neutrophil extracellular traps. Curr Biol 2006, 16:396-400.
27. Berends E.T.M., Horswill A.R., Haste N.M., Monestier M., Nizet V., von Köckritz-Blickwede M. Nuclease expression by Staphylococcus aureus facilitates escape from neutrophil extracellular traps. J Innate Immun 2010, 2:576-586.
28. Wartha F., Beiter K., Albiger B., Fernebro J., Zychlinsky A., Normark S., Henriques-Normark B. Capsule and d-alanylated lipoteichoic acids protect Streptococcus pneumoniae against neutrophil extracellular traps. Cell Microbiol 2007, 9:1162-1171.
29. Casutt-Meyer S., Renzi F., Schmaler M., Jann N.J., Amstutz M., Cornelis G.R. Oligomeric coiled-coil adhesin YadA is a double-edged sword. PLoS ONE 2010, 5:e15159.
30. Semple J.W., Italiano J.E., Freedman J. Platelets and the immune continuum. Nat Rev Immunol 2011, 11:264-274.
31. Clemetson K.J., Clemetson J.M., Proudfoot A.E.I., Power C.A., Baggiolini M., Wells T.N.C. Functional expression of CCR1, CCR3, CCR4, and CXCR4 chemokine receptors on human platelets. Blood 2000, 96:4046-4054.
32. Czapiga M., Gao J., Kirk A., Lekstrom-Himes J. Human platelets exhibit chemotaxis using functional N-formyl peptide receptors. Exp Hematol 2005, 33:73-84.
33. Andonegui G., Kerfoot S.M., McNagny K., Ebbert K.V.J., Patel K.D., Kubes P. Platelets express functional Toll-like receptor-4. Blood 2005, 106:2417-2423.
34. Zhang G., Han J., Welch E.J., Ye R.D., Voyno-Yasenetskaya T.A., Malik A.B., Du X., Li Z. Lipopolysaccharide stimulates platelet secretion and potentiates platelet aggregation via TLR4/MyD88 and the cGMP-dependent protein kinase pathway. J Immunol 2009, 182:7997-8004.
35. Blair P., Rex S., Vitseva O., Beaulieu L., Tanriverdi K., Chakrabarti S., Hayashi C., Genco C.A., Iafrati M., Freedman J.E. Stimulation of toll-like receptor 2 in human platelets induces a thromboinflammatory response through activation of phosphoinositide 3-kinase. Circ Res 2009, 104:346-354.
36. Trier D.A., Gank K.D., Kupferwasser D., Yount N.Y., French W.J., Michelson A.D., Kupferwasser L.I., Xiong Y.Q., Bayer A.S., Yeaman M.R. Platelet antistaphylococcal responses occur through P2X1 and P2Y12 receptor-induced activation and kinocidin release. Infect Immun 2008, 76:5706-5713.
37. Yeaman M. Platelets in defense against bacterial pathogens. Cell Mol Life Sci 2010, 67:525-544. 544.
38. Chiba A., Dascher C.C., Besra G.S., Brenner M.B. Rapid NKT cell responses are self-terminating during the course of microbial infection. J Immunol 2008, 181:2292-2302.
39. Arase H., Arase N., Ogasawara K., Good R.A., Onoè K. An NK1.1+ CD4+8- single-positive thymocyte subpopulation that expresses a highly skewed T-cell antigen receptor V beta family. Proc Natl Acad Sci 1992, 89:6506-6510.
40. Mallevaey T., Clarke A., Scott-Browne J., Young M., Roisman L., Pellicci D., Patel O., Vivian J., Matsuda J., McCluskey J., et al. A molecular basis for NKT cell recognition of CD1d-self-antigen. Immunity 2011, 34:315-326.
41. Muindi K., Cernadas M., Watts G.F.M., Royle L., Neville D.C.A., Dwek R.A., Besra G.S., Rudd P.M., Butters T.D., Brenner M.B. Activation state and intracellular trafficking contribute to the repertoire of endogenous glycosphingolipids presented by CD1d. Proc Natl Acad Sci 2010, 107:3052-3057.
42. Lee W., Moriarty T.J., Wong C.H.Y., Zhou H., Strieter R.M., van Rooijen N., Chaconas G., Kubes P. An intravascular immune response to Borrelia burgdorferi involves Kupffer cells and iNKT cells. Nat Immunol 2010, 11:295-302.
43. Bendelac A., Savage P.B., Teyton L. The biology of NKT cells. Annu Rev Immunol 2007, 25:297-336.
44. Brigl M., Bry L., Kent S.C., Gumperz J.E., Brenner M.B. Mechanism of CD1d-restricted natural killer T cell activation during microbial infection. Nat Immunol 2003, 4:1230-1237.
45. Lisbonne M., L'Helgoualc'h A., Nauwelaers G., Turlin B., Lucas C., Herbelin A., Piquet-Pellorce C., Samson M. Invariant natural killer T-cell-deficient mice display increased CCl4-induced hepatitis associated with CXCL1 over-expression and neutrophil infiltration. Eur J Immunol 2011, 41:1720-1732.
46. Godfrey D.I., Kronenberg M. Going both ways: immune regulation via CD1d-dependent NKT cells. J Clin Invest 2004, 114:1379-1388.
47. Goto M., Murakawa M., Kadoshima-Yamaoka K., Tanaka Y., Nagahira K., Fukuda Y., Nishimura T. Murine NKT cells produce Th17 cytokine interleukin-22. Cell Immunol 2009, 254:81-84.
48. Stevenson H.L., Crossley E.C., Thirumalapura N., Walker D.H., Ismail N. Regulatory roles of CD1d-restricted NKT cells in the induction of toxic shock-like syndrome in an animal model of fatal ehrlichiosis. Infect Immun 2008, 76:1434-1444.
49. Hu C.K., Venet F., Heffernan D.S., Wang Y.L., Horner B., Huang X., Chung C., Gregory S.H., Ayala A. The role of hepatic invariant NKT cells in systemic/local inflammation and mortality during polymicrobial septic shock. J Immunol 2009, 182:2467-2475.
50. Rhee R.J., Carlton S., Lomas J.L., Lane C., Brossay L., Cioffi W.G., Ayala A. Inhibition of CD1d activation suppresses septic mortality: a role for NK-T cells in septic immune dysfunction. J Surg Res 2003, 115:74-81.
51. Brigl M., Tatituri R.V.V., Watts G.F.M., Bhowruth V., Leadbetter E.A., Barton N., Cohen N.R., Hsu F., Besra G.S., Brenner M.B. Innate and cytokine-driven signals, rather than microbial antigens, dominate in natural killer T cell activation during microbial infection. J Exp Med 2011, 208:1163-1177.
52. Mattner J., DeBord K.L., Ismail N., Goff R.D., Cantu C., Zhou D., Saint-Mezard P., Wang V., Gao Y., Yin N., et al. Exogenous and endogenous glycolipid antigens activate NKT cells during microbial infections. Nature 2005, 434:525-529.
53. Velázquez P., Cameron T.O., Kinjo Y., Nagarajan N., Kronenberg M., Dustin M.L. Cutting edge: activation by innate cytokines or microbial antigens can cause arrest of natural killer T cell patrolling of liver sinusoids. J Immunol 2008, 180:2024-2028.
54. Darmoise A., Teneberg S., Bouzonville L., Brady R.O., Beck M., Kaufmann S.H.E., Winau F. Lysosomal α-galactosidase controls the generation of self lipid antigens for natural killer T cells. Immunity 2010, 33:216-228.