Monocyte and macrophage biology: an overview

Exploring the full spectrum of macrophage activation

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The chemokine system in diverse forms of macrophage activation and polarization

MANTOVANI, A., SICA, A., SOZZANI, S., ALLAVENA, P., VECCHI, A., & LOCATI, M. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.09.015 · Cited by 6,534 · see citing works

Monocyte and macrophage heterogeneity

Gordon, S., & Taylor, P. R. (2005) · Nature Reviews Immunology · doi:10.1038/nri1733 · Cited by 5,190 · see citing works

Blood Monocytes Consist of Two Principal Subsets with Distinct Migratory Properties

Geissmann, F., Jung, S., & Littman, D. R. (2003) · Immunity · doi:10.1016/s1074-7613(03)00174-2 · Cited by 3,366 · see citing works

Alternative Activation of Macrophages: An Immunologic Functional Perspective

Martinez, F. O., Helming, L., & Gordon, S. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132532 · Cited by 2,745 · see citing works

Analysis of Fractalkine Receptor CX₃CR1 Function by Targeted Deletion and Green Fluorescent Protein Reporter Gene Insertion

Jung, S., Aliberti, J., Graemmel, P., Sunshine, M. J., Kreutzberg, G. W., Sher, A., & Littman, D. R. (2000) · Molecular and Cellular Biology · doi:10.1128/mcb.20.11.4106-4114.2000 · Cited by 2,632 · see citing works

Identification of splenic reservoir monocytes and their deployment to inflammatory sites

Swirski, F. K., Nahrendorf, M., Etzrodt, M., Wildgruber, M., Cortez-Retamozo, V., Panizzi, P., Figueiredo, J.-L., Kohler, R. H., Chudnovskiy, A., Waterman, P., et al. (2009) · Science · doi:10.1126/science.1175202 · Cited by 2,221 · see citing works

Monitoring of Blood Vessels and Tissues by a Population of Monocytes with Patrolling Behavior

Auffray, C., Fogg, D., Garfa, M., Elain, G., Join-Lambert, O., Kayal, S., Sarnacki, S., Cumano, A., Lauvau, G., & Geissmann, F. (2007) · Science · doi:10.1126/science.1142883 · Cited by 1,973 · see citing works

How dying cells alert the immune system to danger

Kono, H., & Rock, K. L. (2008) · Nature Reviews Immunology · doi:10.1038/nri2215 · Cited by 1,737 · see citing works

Monocyte emigration from bone marrow during bacterial infection requires signals mediated by chemokine receptor CCR2

Serbina, N. V., & Pamer, E. G. (2006) · Nature Immunology · doi:10.1038/ni1309 · Cited by 1,658 · see citing works

Blood Monocytes: Development, Heterogeneity, and Relationship with Dendritic Cells

Auffray, C., Sieweke, M. H., & Geissmann, F. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132557 · Cited by 1,647 · see citing works

A blast from the past: clearance of apoptotic cells regulates immune responses

Savill, J., Dransfield, I., Gregory, C. D., & Haslett, C. (2002) · Nature reviews. Immunology · doi:10.1038/nri957 · Cited by 1,574 · see citing works

THE ORIGIN AND KINETICS OF MONONUCLEAR PHAGOCYTES

van Furth, R., & Cohn, Z. A. (1968) · The Journal of Experimental Medicine · doi:10.1084/jem.128.3.415 · Cited by 1,564 · see citing works

CELLULAR RESISTANCE TO INFECTION

Mackaness, G. B. (1962) · The Journal of Experimental Medicine · doi:10.1084/jem.116.3.381 · Cited by 1,368 · see citing works

MIF is a noncognate ligand of CXC chemokine receptors in inflammatory and atherogenic cell recruitment

Bernhagen, J., Krohn, R. M., Lue, H., Gregory, J. L., Zernecke, A., Koenen, R. R., Dewor, M., Georgiev, I., Schober, A., Leng, L., et al. (2007) · Nature Medicine · doi:10.1038/nm1567 · Cited by 1,272 · see citing works

Steady-state and inflammatory dendritic-cell development

Shortman, K., & Naik, S. H. (2006) · Nature reviews. Immunology · doi:10.1038/nri1996 · Cited by 1,180 · see citing works

The JAK-STAT Signaling Pathway: Input and Output Integration

Murray, P. J. (2007) · The Journal of Immunology · doi:10.4049/jimmunol.178.5.2623 · Cited by 1,179 · see citing works

The mononuclear phagocyte system: a new classification of macrophages, monocytes, and their precursor cells.

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Subpopulations of Mouse Blood Monocytes Differ in Maturation Stage and Inflammatory Response

Sunderkötter, C., Nikolic, T., Dillon, M. J., van Rooijen, N., Stehling, M., Drevets, D. A., & Leenen, P. J. M. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.172.7.4410 · Cited by 1,124 · see citing works

Toll-like receptor–mediated cytokine production is differentially regulated by glycogen synthase kinase 3

Martin, M., Rehani, K., Jope, R. S., & Michalek, S. M. (2005) · Nature Immunology · doi:10.1038/ni1221 · Cited by 1,080 · see citing works

The CD14+ CD16+ blood monocytes: their role in infection and inflammation

Ziegler‐Heitbrock, L. (2006) · Journal of Leukocyte Biology · doi:10.1189/jlb.0806510 · Cited by 1,045 · see citing works

Identification and characterization of a novel monocyte subpopulation in human peripheral blood

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Macrophages regulate salt-dependent volume and blood pressure by a vascular endothelial growth factor-C–dependent buffering mechanism

Machnik, A., Neuhofer, W., Jantsch, J., Dahlmann, A., Tammela, T., Machura, K., Park, J.-K., Beck, F.-X., Müller, D. N., Derer, W., et al. (2009) · Nature Medicine · doi:10.1038/nm.1960 · Cited by 953 · see citing works

Cross-regulation of Signaling Pathways by Interferon-γ: Implications for Immune Responses and Autoimmune Diseases

Hu, X., & Ivashkiv, L. B. (2009) · Immunity · doi:10.1016/j.immuni.2009.09.002 · Cited by 928 · see citing works

Origin of the Lamina Propria Dendritic Cell Network

Bogunovic, M., Ginhoux, F., Helft, J., Shang, L., Hashimoto, D., Greter, M., Liu, K., Jakubzick, C., Ingersoll, M. A., Leboeuf, M., et al. (2009) · Immunity · doi:10.1016/j.immuni.2009.08.010 · Cited by 859 · see citing works

Cytokine Signaling Modules in Inflammatory Responses

O’Shea, J. J., & Murray, P. J. (2008) · Immunity · doi:10.1016/j.immuni.2008.03.002 · Cited by 819 · see citing works

The TSC-mTOR Signaling Pathway Regulates the Innate Inflammatory Response

Weichhart, T., Costantino, G., Poglitsch, M., Rosner, M., Zeyda, M., Stuhlmeier, K. M., Kolbe, T., Stulnig, T. M., Hörl, W. H., Hengstschläger, M., et al. (2008) · Immunity · doi:10.1016/j.immuni.2008.08.012 · Cited by 801 · see citing works

Hepatic recruitment of the inflammatory Gr1+ monocyte subset upon liver injury promotes hepatic fibrosis

Karlmark, K. R., Weiskirchen, R., Zimmermann, H. W., Gassler, N., Ginhoux, F., Weber, C., Merad, M., Luedde, T., Trautwein, C., & Tacke, F. (2009) · Hepatology · doi:10.1002/hep.22950 · Cited by 782 · see citing works

The origin and development of nonlymphoid tissue CD103+ DCs

Ginhoux, F., Liu, K., Helft, J., Bogunovic, M., Greter, M., Hashimoto, D., Price, J. G., Yin, N., Bromberg, J. S., Lira, S. A., et al. (2009) · The Journal of Experimental Medicine · doi:10.1084/jem.20091756 · Cited by 744 · see citing works

Langerhans cells arise from monocytes in vivo

Ginhoux, F., Tacke, F., Angeli, V., Bogunovic, M., Loubeau, M., Dai, X.-M., Stanley, E. R., Randolph, G. J., & Mérad, M. (2006) · Nature Immunology · doi:10.1038/ni1307 · Cited by 741 · see citing works

Comparison of gene expression profiles between human and mouse monocyte subsets

Ingersoll, M. A., Spanbroek, R., Lottaz, C., Gautier, E. L., Frankenberger, M., Hoffmann, R. F. G., Lang, R., Haniffa, M. A., Collin, M. P., Tacke, F., et al. (2009) · Blood · doi:10.1182/blood-2009-07-235028 · Cited by 731 · see citing works

Combined Inhibition of CCL2, CX3CR1, and CCR5 Abrogates Ly6Chi and Ly6Clo Monocytosis and Almost Abolishes Atherosclerosis in Hypercholesterolemic Mice

Combadière, C., Potteaux, S., Rodero, M., Simon, T., Pézard, A., Esposito, B., Merval, R., Proudfoot, A., Tedgui, A., & Mallat, Z. (2008) · Circulation · doi:10.1161/circulationaha.107.745091 · Cited by 714 · see citing works

A macrophage colony-stimulating factor receptor–green fluorescent protein transgene is expressed throughout the mononuclear phagocyte system of the mouse

Sasmono, R. T., Oceandy, D., Pollard, J. W., Tong, W., Pavli, P., Wainwright, B. J., Ostrowski, M. C., Himes, S. R., & Hume, D. A. (2003) · Blood · doi:10.1182/blood-2002-02-0569 · Cited by 662 · see citing works

Monocytes give rise to mucosal, but not splenic, conventional dendritic cells

Varol, C., Landsman, L., Fogg, D. K., Greenshtein, L., Gildor, B., Margalit, R., Kalchenko, V., Geissmann, F., & Jung, S. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20061011 · Cited by 627 · see citing works

The macrophage: Past, present and future

Gordon, S. (2007) · European Journal of Immunology · doi:10.1002/eji.200737638 · Cited by 625 · see citing works

Transcription factors in myeloid development: balancing differentiation with transformation

Rosenbauer, F., & Tenen, D. G. (2007) · Nature Reviews Immunology · doi:10.1038/nri2024 · Cited by 606 · see citing works

Demonstration and characterization of Ia-positive dendritic cells in the interstitial connective tissues of rat heart and other tissues, but not brain.

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Adhesion mechanisms regulating the migration of monocytes

Imhof, B. A., & Aurrand‐Lions, M. (2004) · Nature reviews. Immunology · doi:10.1038/nri1375 · Cited by 584 · see citing works

Galectin-3 Expression and Secretion Links Macrophages to the Promotion of Renal Fibrosis

Henderson, N. C., Mackinnon, A. C., Farnworth, S. L., Kipari, T., Haslett, C., Iredale, J. P., Liu, F.-T., Hughes, J., & Sethi, T. (2008) · The American Journal of Pathology · doi:10.2353/ajpath.2008.070726 · Cited by 562 · see citing works

Macrophages as APC and the Dendritic Cell Myth

Hume, D. A. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.9.5829 · Cited by 504 · see citing works

WNT7b mediates macrophage-induced programmed cell death in patterning of the vasculature

Lobov, I. B., Rao, S., Carroll, T. J., Vallance, J. E., Ito, M., Ondr, J. K., Kurup, S., Glass, D. A., Patel, M. S., Shu, W., et al. (2005) · Nature · doi:10.1038/nature03928 · Cited by 429 · see citing works

The mononuclear phagocyte system revisited

Hume, D. A., Ross, I. L., Himes, S. R., Sasmono, R. T., Wells, C. A., & Ravasi, T. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.72.4.621 · Cited by 425 · see citing works

Dendritic cell subsets in primary and secondary T cell responses at body surfaces

Heath, W. R., & Carbone, F. (2009) · Nature Immunology · doi:10.1038/ni.1822 · Cited by 420 · see citing works

The chemokine receptors CCR2 and CX3CR1 mediate monocyte/macrophage trafficking in kidney ischemia–reperfusion injury

Li, L., Huang, L., Sung, S. J., Vergis, A. L., Rosin, D. L., Rose, C. E., Lobo, P. I., & Okusa, M. D. (2008) · Kidney International · doi:10.1038/ki.2008.500 · Cited by 393 · see citing works

The concept of the activated macrophage.

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Biology of Lung Dendritic Cells at the Origin of Asthma

Lambrecht, B. N., & Hammad, H. (2009) · Immunity · doi:10.1016/j.immuni.2009.08.008 · Cited by 372 · see citing works

Resident dendritic cells are the predominant TNF-secreting cell in early renal ischemia–reperfusion injury

Dong, X., Swaminathan, S., Bachman, L. A., Croatt, A. J., Nath, K. A., & Griffin, M. D. (2007) · Kidney International · doi:10.1038/sj.ki.5002132 · Cited by 363 · see citing works

The CD16+ (FcγRIII+) Subset of Human Monocytes Preferentially Becomes Migratory Dendritic Cells in a Model Tissue Setting

Randolph, G. J., Sánchez‐Schmitz, G., Liebman, R. M., & Schäkel, K. (2002) · The Journal of Experimental Medicine · doi:10.1084/jem.20011608 · Cited by 357 · see citing works

Heterogeneity of human peripheral blood monocyte subsets

Grage‐Griebenow, E., FLAD, H.-D., & Ernst, M. (2001) · Journal of Leukocyte Biology · doi:10.1189/jlb.69.1.11 · Cited by 349 · see citing works

Resolution-phase macrophages possess a unique inflammatory phenotype that is controlled by cAMP

Byström, J., Evans, I. M., Newson, J., Stables, M. J., Toor, I. S., van Rooijen, N., Crawford, M., Colville‐Nash, P., Farrow, S. N., & Gilroy, D. W. (2008) · Blood · doi:10.1182/blood-2007-12-129767 · Cited by 335 · see citing works

Bone Marrow Ly6Chigh Monocytes Are Selectively Recruited to Injured Kidney and Differentiate into Functionally Distinct Populations

Lin, S., Castaño, A. P., Nowlin, B. T., Lupher, M., & Duffield, J. S. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0901473 · Cited by 326 · see citing works

CX3CR1+ interstitial dendritic cells form a contiguous network throughout the entire kidney

Soos, T. J., Sims, T. N., Barisoni, L. M. C., Lin, K. L., Littman, D. R., Dustin, M. L., & Nelson, P. J. (2006) · Kidney International · doi:10.1038/sj.ki.5001567 · Cited by 309 · see citing works

Signal integration between IFNγ and TLR signalling pathways in macrophages

Schroder, K., Sweet, M. J., & Hume, D. A. (2006) · Immunobiology · doi:10.1016/j.imbio.2006.05.007 · Cited by 288 · see citing works

Phagocytosis and comparative innate immunity: learning on the fly

Stuart, L. M., & Ezekowitz, R. A. B. (2008) · Nature reviews. Immunology · doi:10.1038/nri2240 · Cited by 288 · see citing works

The multiple facets of mTOR in immunity

Weichhart, T., & Säemann, M. D. (2009) · Trends in Immunology · doi:10.1016/j.it.2009.02.002 · Cited by 260 · see citing works

Conditional Ablation of Macrophages Halts Progression of Crescentic Glomerulonephritis

Duffield, J. S., Tipping, P. G., Kipari, T. M. J., Cailhier, J., Clay, S., Lang, R. A., Bonventre, J. V., & Hughes, J. (2005) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)61209-6 · Cited by 241 · see citing works

Identification and Functional Characterization of Dendritic Cells in the Healthy Murine Kidney and in Experimental Glomerulonephritis

Krüger, T., Benke, D., Eitner, F., Lang, A., Wirtz, M., Hamilton‐Williams, E. E., Engel, D. R., Giese, B., Müller‐Newen, G., Floege, J., et al. (2004) · Journal of the American Society of Nephrology · doi:10.1097/01.asn.0000114553.36258.91 · Cited by 240 · see citing works

Opinions

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Characterisation and trophic functions of murine embryonic macrophages based upon the use of a Csf1r–EGFP transgene reporter

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Kidney dendritic cell activation is required for progression of renal disease in a mouse model of glomerular injury

Heymann, F., Meyer‐Schwesinger, C., Hamilton‐Williams, E. E., Hammerich, L., Panzer, U., Kaden, S., Quaggin, S. E., Floege, J., Gröne, H., & Kurts, C. (2009) · Journal of Clinical Investigation · doi:10.1172/jci38399 · Cited by 207 · see citing works

Selective mobilization of CD14+CD16+ monocytes by exercise

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Mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80. Identification of resident macrophages in renal medullary and cortical interstitium and the juxtaglomerular complex

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Expanded CD14+CD16+Monocyte Subpopulation in Patients with Acute and Chronic Infections Undergoing Hemodialysis

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Initial Cytokine Exposure Determines Function of Macrophages and Renders Them Unresponsive to Other Cytokines

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MafB Restricts M-CSF-Dependent Myeloid Commitment Divisions of Hematopoietic Stem Cells

Sarrazin, S., Mossadegh‐Keller, N., Fukao, T., Aziz, A., Mourcin, F., Vanhille, L., Modis, L. K., Kastner, P., Chan, S. H., Duprez, E., et al. (2009) · Cell · doi:10.1016/j.cell.2009.04.057 · Cited by 177 · see citing works

Unique Expression of Suppressor of Cytokine Signaling 3 Is Essential for Classical Macrophage Activation in Rodents In Vitro and In Vivo

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Systems biology of innate immunity

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Selective depletion of CD14+ CD16+ monocytes by glucocorticoid therapy

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Relationships between Distinct Blood Monocyte Subsets and Migrating Intestinal Lymph Dendritic Cells In Vivo under Steady-State Conditions

Yrlid, U., Jenkins, C. D., & MacPherson, G. G. (2006) · The Journal of Immunology · doi:10.4049/jimmunol.176.7.4155 · Cited by 149 · see citing works

The mononuclear phagocyte system of the mouse defined by immunohistochemical localisation of antigen F4/80

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The Porcine 2A10 Antigen Is Homologous to Human CD163 and Related to Macrophage Differentiation

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Compartment specific expression of dendritic cell markers in human glomerulonephritis

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Renal Dendritic Cells Stimulate IL-10 Production and Attenuate Nephrotoxic Nephritis

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Quantification of dendritic cell subsets in human renal tissue under normal and pathological conditions

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Mechanism of glucocorticoid-induced depletion of human CD14+CD16+ monocytes

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The Monoclonal Antimonocyte Antibody My4 Stains B Lymphocytes and Two Distinct Monocyte Subsets in Human Peripheral Blood

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Proteasomal Processing of Albumin by Renal Dendritic Cells Generates Antigenic Peptides

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Inhibition of Macrophage Nuclear Factor-κB Leads to a Dominant Anti-Inflammatory Phenotype that Attenuates Glomerular Inflammation in Vivo

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Transendothelial migration of CD16+ monocytes in response to fractalkine under constitutive and inflammatory conditions

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CCR2 Mediates Homeostatic and Inflammatory Release of Gr1high Monocytes from the Bone Marrow, but Is Dispensable for Bladder Infiltration in Bacterial Urinary Tract Infection

Engel, D. R., Maurer, J., Tittel, A. P., Weisheit, C. K., Cavlar, T., Schumak, B., Limmer, A., van Rooijen, N., Trautwein, C., Tacke, F., et al. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.8.5579 · Cited by 93 · see citing works

New observations on the trafficking and diapedesis of monocytes

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Membrane Molecules as Differentiation Antigens of Murine Macrophages

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The Kidney-Renal Lymph Node-System Contributes to Cross-Tolerance against Innocuous Circulating Antigen1

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Mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80.

Hume, D., & Gordon, S. (1983) · The Journal of Experimental Medicine · Cited by 81 · see citing works

Strong depletion of CD14+CD16+ monocytes during haemodialysis treatment

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The role of SHIP1 in macrophage programming and activation

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Depletion of Cells of Monocyte Lineage Prevents Loss of Renal Microvasculature in Murine Kidney Transplantation

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Identification of Two Subpopulations of Rat Monocytes Expressing Disparate Molecular Forms and Quantities of CD43

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CCR2 and CXCR4 regulate peripheral blood monocyte pharmacodynamics and link to efficacy in experimental autoimmune encephalomyelitis

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