Phagocyte partnership during the onset and resolution of inflammation

Oliver Soehnlein; Lennart Lindbom

doi:10.1038/nri2779

journal article Jun 01, 2010

Phagocyte partnership during the onset and resolution of inflammation

Oliver Soehnlein

Lennart Lindbom

Nature Reviews Immunology Vol. 10 No. 6 pp. 427-439 · Springer Science and Business Media LLC

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References

137

[1]

Nathan, C. Neutrophils and immunity: challenges and opportunities. Nature Rev. Immunol. 6, 173–182 (2006). 10.1038/nri1785

[2]

Ingersoll, M. A. et al. Comparison of gene expression profiles between human and mouse monocyte subsets. Blood 115, e10–e19 (2010). 10.1182/blood-2009-07-235028

[3]

Ziegler-Heitbrock, L. The CD14+ CD16+ blood monocytes: their role in infection and inflammation. J. Leukoc. Biol. 81, 584–592 (2007). 10.1189/jlb.0806510

[4]

Auffray, C. et al. Monitoring of blood vessels and tissues by a population of monocytes with patrolling behavior. Science 317, 666–670 (2007). The first paper to show the potential importance of non-classical monocytes during the start of an inflammatory response in the mouse. 10.1126/science.1142883

[5]

The healing myocardium sequentially mobilizes two monocyte subsets with divergent and complementary functions

Matthias Nahrendorf, Filip K. Swirski, Elena Aikawa et al.

The Journal of Experimental Medicine 2007 10.1084/jem.20070885

[6]

Zhao, C. et al. Identification of novel functional differences in monocyte subsets using proteomic and transcriptomic methods. J. Proteome Res. 8, 4028–4038 (2009). 10.1021/pr900364p

[7]

Frankenberger, M., Sternsdorf, T., Pechumer, H., Pforte, A. & Ziegler-Heitbrock, H. W. Differential cytokine expression in human blood monocyte subpopulations: a polymerase chain reaction analysis. Blood 87, 373–377 (1996). 10.1182/blood.v87.1.373.373

[8]

Belge, K. U. et al. The proinflammatory CD14+CD16+DR++ monocytes are a major source of TNF. J. Immunol. 168, 3536–3542 (2002). 10.4049/jimmunol.168.7.3536

[9]

Tacke, F. et al. Monocyte subsets differentially employ CCR2, CCR5, and CX3CR1 to accumulate within atherosclerotic plaques. J. Clin. Invest. 117, 185–194 (2007). 10.1172/jci28549

[10]

An, G. et al. P-selectin glycoprotein ligand-1 is highly expressed on Ly-6Chi monocytes and a major determinant for Ly-6Chi monocyte recruitment to sites of atherosclerosis in mice. Circulation 117, 3227–3237 (2008). 10.1161/circulationaha.108.771048

[11]

Soehnlein, O. & Weber, C. Myeloid cells in atherosclerosis: initiators and decision shapers. Semin. Immunopathol. 31, 35–47 (2009). 10.1007/s00281-009-0141-z

[12]

Geissmann, F., Jung, S. & Littman, D. R. Blood monocytes consist of two principal subsets with distinct migratory properties. Immunity 19, 71–82 (2003). This paper proves the existence of two mouse monocyte subsets with phenotypical and functional differences. 10.1016/s1074-7613(03)00174-2

[13]

Yona, S. & Jung, S. Monocytes: subsets, origins, fates and functions. Curr. Opin. Hematol. 17, 53–59 (2010). 10.1097/moh.0b013e3283324f80

[14]

Immunology's foundation: the 100-year anniversary of the Nobel Prize to Paul Ehrlich and Elie Metchnikoff

Stefan H E Kaufmann

Nature Immunology 2008 10.1038/ni0708-705

[15]

Dale, D. C., Boxer, L. & Liles, W. C. The phagocytes: neutrophils and monocytes. Blood 112, 935–945 (2008). 10.1182/blood-2007-12-077917

[16]

Kantari, C., Pederzoli-Ribeil, M. & Witko-Sarsat, V. The role of neutrophils and monocytes in innate immunity. Contrib. Microbiol. 15, 118–146 (2008). 10.1159/000136335

[17]

Akashi, K., Traver, D., Miyamoto, T. & Weissman, I. L. A clonogenic common myeloid progenitor that gives rise to all myeloid lineages. Nature 404, 193–197 (2000). 10.1038/35004599

[18]

Ma, Q., Jones, D. & Springer, T. A. The chemokine receptor CXCR4 is required for the retention of B lineage and granulocytic precursors within the bone marrow microenvironment. Immunity 10, 463–471 (1999). 10.1016/s1074-7613(00)80046-1

[19]

Suratt, B. T. et al. Role of the CXCR4/SDF-1 chemokine axis in circulating neutrophil homeostasis. Blood 104, 565–571 (2004). 10.1182/blood-2003-10-3638

[20]

Serbina, N. V. & Pamer, E. G. Monocyte emigration from bone marrow during bacterial infection requires signals mediated by chemokine receptor CCR2. Nature Immunol. 7, 311–317 (2006). 10.1038/ni1309

[21]

Martin, C. et al. Chemokines acting via CXCR2 and CXCR4 control the release of neutrophils from the bone marrow and their return following senescence. Immunity 19, 583–593 (2003). 10.1016/s1074-7613(03)00263-2

[22]

Swirski, F. K. et al. Identification of splenic reservoir monocytes and their deployment to inflammatory sites. Science 325, 612–616 (2009). 10.1126/science.1175202

[23]

Nathan, C. & Shiloh, M. U. Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens. Proc. Natl Acad. Sci. USA 97, 8841–8848 (2000). 10.1073/pnas.97.16.8841

[24]

Kono, H. & Rock, K. L. How dying cells alert the immune system to danger. Nature Rev. Immunol. 8, 279–289 (2008). 10.1038/nri2215

[25]

Medzhitov, R. Recognition of microorganisms and activation of the immune response. Nature 449, 819–826 (2007). 10.1038/nature06246

[26]

Passlick, B., Flieger, D. & Ziegler-Heitbrock, H. W. Identification and characterization of a novel monocyte subpopulation in human peripheral blood. Blood 74, 2527–2534 (1989). 10.1182/blood.v74.7.2527.2527

[27]

Auffray, C., Sieweke, M. H. & Geissmann, F. Blood monocytes: development, heterogeneity, and relationship with dendritic cells. Annu. Rev. Immunol. 27, 669–692 (2009). 10.1146/annurev.immunol.021908.132557

[28]

Soehnlein, O., Lindbom, L. & Weber, C. Mechanisms underlying neutrophil-mediated monocyte recruitment. Blood 114, 4613–4623 (2009). 10.1182/blood-2009-06-221630

[29]

Mincle is an ITAM-coupled activating receptor that senses damaged cells

Sho Yamasaki, Eri Ishikawa, Machie Sakuma et al.

Nature Immunology 2008 10.1038/ni.1651

[30]

Hara, H. et al. The adaptor protein CARD9 is essential for the activation of myeloid cells through ITAM-associated and Toll-like receptors. Nature Immunol. 8, 619–629 (2007). 10.1038/ni1466

[31]

Scaffidi, P., Misteli, T. & Bianchi, M. E. Release of chromatin protein HMGB1 by necrotic cells triggers inflammation. Nature 418, 191–195 (2002). 10.1038/nature00858

[32]

Bianchi, M. E. HMGB1 loves company. J. Leukoc. Biol. 86, 573–576 (2009). 10.1189/jlb.1008585

[33]

Tian, J. et al. Toll-like receptor 9-dependent activation by DNA-containing immune complexes is mediated by HMGB1 and RAGE. Nature Immunol. 8, 487–496 (2007). 10.1038/ni1457

[34]

Yanai, H. et al. HMGB proteins function as universal sentinels for nucleic-acid-mediated innate immune responses. Nature 462, 99–103 (2009). 10.1038/nature08512

[35]

Chen, G. Y., Tang, J., Zheng, P. & Liu, Y. CD24 and Siglec-10 selectively repress tissue damage-induced immune responses. Science 323, 1722–1725 (2009). This study elucidates a new mechanism by which the immune system discriminates between infection and tissue injury. 10.1126/science.1168988

[36]

Liu, Y., Chen, G. Y. & Zheng, P. CD24-Siglec G/10 discriminates danger- from pathogen-associated molecular patterns. Trends Immunol. 30, 557–561 (2009). 10.1016/j.it.2009.09.006

[37]

García-Ramallo, E. et al. Resident cell chemokine expression serves as the major mechanism for leukocyte recruitment during local inflammation. J. Immunol. 169, 6467–6473 (2002). 10.4049/jimmunol.169.11.6467

[38]

Beck-Schimmer, B. et al. Alveolar macrophages regulate neutrophil recruitment in endotoxin-induced lung injury. Respir. Res. 6, 61 (2005). 10.1186/1465-9921-6-61

[39]

Cailhier, J. F. et al. Conditional macrophage ablation demonstrates that resident macrophages initiate acute peritoneal inflammation. J. Immunol. 174, 2336–2342 (2005). 10.4049/jimmunol.174.4.2336

[40]

Resident Pleural Macrophages Are Key Orchestrators of Neutrophil Recruitment in Pleural Inflammation

Jean François Cailhier, Deborah A. Sawatzky, Tiina Kipari et al.

American Review of Respiratory Disease 2006 10.1164/rccm.200504-538oc

[41]

Ajuebor, M. N. et al. Role of resident peritoneal macrophages and mast cells in chemokine production and neutrophil migration in acute inflammation: evidence for an inhibitory loop involving endogenous IL-10. J. Immunol. 162, 1685–1691 (1999). 10.4049/jimmunol.162.3.1685

[42]

Yamamoto, S. et al. TRPM2-mediated Ca2+ influx induces chemokine production in monocytes that aggravates inflammatory neutrophil infiltration. Nature Med. 14, 738–747 (2008). 10.1038/nm1758

[43]

Neutrophil gelatinase B potentiates interleukin-8 tenfold by aminoterminal processing, whereas it degrades CTAP-III, PF-4, and GRO-α and leaves RANTES and MCP-2 intact

Philippe E. Van den Steen, Paul Proost, Anja Wuyts et al.

Blood 2000 10.1182/blood.v96.8.2673

[44]

Tester, A. M. et al. LPS responsiveness and neutrophil chemotaxis in vivo require PMN MMP-8 activity. PLoS ONE 2, e312 (2007). 10.1371/journal.pone.0000312

[45]

Prostaglandins and Leukotrienes: Advances in Eicosanoid Biology

Colin D. Funk

Science 2001 10.1126/science.294.5548.1871

[46]

Dahlén, S. E. et al. Leukotrienes promote plasma leakage and leukocyte adhesion in postcapillary venules: in vivo effects with relevance to the acute inflammatory response. Proc. Natl Acad. Sci. USA 78, 3887–3891 (1981). 10.1073/pnas.78.6.3887

[47]

Schoenberger, S. P. BLT for speed. Nature Immunol. 4, 937–939 (2003). 10.1038/ni1003-937

[48]

Tager, A. M. & Luster, A. D. BLT1 and BLT2: the leukotriene B4 receptors. Prostaglandins Leukot. Essent. Fatty Acids. 69, 123–134 (2003). 10.1016/s0952-3278(03)00073-5

[49]

Borregaard, N. & Cowland, J. B. Granules of the human neutrophilic polymorphonuclear leukocyte. Blood 89, 3503–3521 (1997). 10.1182/blood.v89.10.3503

[50]

Faurschou, M. & Borregaard, N. Neutrophil granules and secretory vesicles in inflammation. Microbes Infect. 5, 1317–1327 (2003). 10.1016/j.micinf.2003.09.008

Showing 50 of 137 references

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Published: Jun 01, 2010
Vol/Issue: 10(6)
Pages: 427-439
License: View

Authors

Department of Physiology and Pharmacology, Karolinska Institute, Stockholm, Sweden;

Cite This Article

Oliver Soehnlein, Lennart Lindbom (2010). Phagocyte partnership during the onset and resolution of inflammation. Nature Reviews Immunology, 10(6), 427-439. https://doi.org/10.1038/nri2779

Phagocyte partnership during the onset and resolution of inflammation

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