Characterization of murine lung interstitial macrophages in comparison with alveolar macrophages in vitro
Abstract
The present study was performed to characterize the immunologic potential of interstitial macrophages (INT) in comparison with alveolar macrophages (AL). The data showed that AL, compared with INT, have a more efficient phagocytic potential. In addition, they have a strong microbicidal activity and secrete large amounts of reactive oxygen radicals, nitric oxides, TNF, and IFN on appropriate stimulation. They also exert strong tumoricidal and parasiticidal activities. In contrast, INT are more efficient in releasing immunoregulatory cytokines such as IL-1 and IL-6. As determined by Ab staining, INT express more MHC class II molecules and are more effective in functioning as accessory cells for mitogen-stimulated lymphocyte proliferation compared with AL. Thus, AL appear to be particularly effective as nonspecific first line defense cells against infectious agents, whereas INT are equipped to cooperate with interstitial lymphocytes in inducing a specific immune reaction.
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Resident alveolar macrophages have high phagocytic capacity.
“Among host innate immune players, resident alveolar macrophages (AMs) are considered to be the most important first line of defense against respiratory pneumococcal infections (13), through their high phagocytic capacity (14–16).”
From Depletion of alveolar macrophages during influenza infection facilitates bacterial superinfections (2013) · cites this paper as [14]
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Bedoret, D., Wallemacq, H., Marichal, T., Desmet, C., Quesada Calvo, F., Henry, E., Closset, R., Dewals, B., Thielen, C., Gustin, P., et al. (2009) · Journal of Clinical Investigation · doi:10.1172/jci39717 · Cited by 399 · see citing works
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Geiser, M. (2010) · Journal of Aerosol Medicine and Pulmonary Drug Delivery · doi:10.1089/jamp.2009.0797 · Cited by 364 · see citing works
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Byrne, A. J., Maher, T. M., & Lloyd, C. M. (2016) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2016.02.004 · Cited by 314 · see citing works
“Global IL-10 knockout mice are also protected from silica or bleomycin-induced fibrosis [99].”
InfluentialAlveolar Macrophages Have a Protective Antiinflammatory Role during Murine Pneumococcal Pneumonia
Knapp, S., Leemans, J. C., Florquin, S., Branger, J., Maris, N. A., Pater, J. M., van Rooijen, N., & van der Poll, T. (2003) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200207-698oc · Cited by 302 · see citing works
“Am J Respir Cell Mol Biol 19(6):867-74.”
BackgroundFunctional heterogeneity in liver and lung macrophages
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Knoll, R., Schultze, J. L., & Schulte-Schrepping, J. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.720109 · Cited by 269 · see citing works
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Tian, W., Jiang, X., Tamošiūnienė, R., Sung, Y. K., Qian, J., Dhillon, G. S., Gera, L., Farkas, L., Rabinovitch, M., Zamanian, R. T., et al. (2013) · Science Translational Medicine · doi:10.1126/scitranslmed.3006674 · Cited by 262 · see citing works
“We established a macrophage-PAEC coculture system that used pulmonary macrophages purified separately from the interstitial and alveolar compartments, as described (26, 27).”
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Perivascular macrophages in health and disease
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Role of alveolar macrophages in chronic obstructive pulmonary disease
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“AMs are considered to be major effector cells in innate host defense against inhaled irritants by virtue of their phagocytic ability (9).”
BackgroundDockrell, D. H., Marriott, H. M., Prince, L. R., Ridger, V. C., Ince, P. G., Hellewell, P. G., & Whyte, M. K. B. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.10.5380 · Cited by 239 · see citing works
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BackgroundDifferentiation and heterogeneity in the mononuclear phagocyte system
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Leemans, J. C., Juffermans, N. P., Florquin, S., van Rooijen, N., Vervoordeldonk, M. J., Verbon, A., van Deventer, S. J. H., & van der Poll, T. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.166.7.4604 · Cited by 216 · see citing works
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Saunders, B., Frank, A., Orme, I., & Cooper, A. (2000) · Infection and Immunity · doi:10.1128/iai.68.6.3322-3326.2000 · Cited by 240 · see citing works
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Girodet, P., Nguyen, D., Mancini, J. D., Hundal, M., Zhou, X., Israel, E., & Cernadas, M. (2016) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2015-0295oc · Cited by 205 · see citing works
The alveolar macrophages in asthma: a double-edged sword
Balhara, J., & GOUNNI, A. S. (2012) · Mucosal Immunology · doi:10.1038/mi.2012.74 · Cited by 205 · see citing works
Oshima, T., Laroux, F. S., Coe, L. L., Morise, Z., Kawachi, S., Bauer, P. R., Grisham, M. B., Specian, R. D., Carter, P., Jennings, S. R., et al. (2001) · Microvascular Research · doi:10.1006/mvre.2000.2288 · Cited by 190 · see citing works
Alveolar macrophages regulate neutrophil recruitment in endotoxin-induced lung injury
Beck‐Schimmer, B., Schwendener, R. A., Pasch, T., Reyes, L., Booy, C., & Schimmer, R. C. (2005) · Respiratory Research · doi:10.1186/1465-9921-6-61 · Cited by 190 · see citing works
“While most of the inflammatory mediators such as TNF-α, IL-1β and IL-6 were significantly increased upon stimulation of the HBEC/AM-co-culture, MCP-1 production was decreased.”
BackgroundLung Interstitial Macrophages: Past, Present, and Future
Schyns, J., Bureau, F., & Marichal, T. (2018) · Journal of Immunology Research · doi:10.1155/2018/5160794 · Cited by 166 · see citing works
“Upon ex vivo stimulation with lipopolysaccharide (LPS), AM displayed greater cytotoxic and antimicrobial activities than TM, while TM secreted more interleukin(IL-) 1 and IL-6, inmice [13] and rats [16].”
BackgroundHe, X., Mekasha, S., Mavrogiorgos, N. C., Fitzgerald, K. A., Lien, E., & Ingalls, R. R. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903937 · Cited by 157 · see citing works
Florentin, J., Coppin, E., Vasamsetti, S. B., Zhao, J., Tai, Y., Tang, Y., Zhang, Y., Watson, A. M. M., Sembrat, J., Rojas, M. M., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701287 · Cited by 162 · see citing works
“mAbs, including anti-CD45 (HI30), anti-CD14 (61D3), anti-CD16 (3G8), anti-CD24 (ML5), anti-HLA-DR (G46-6), antiCD169 (7-239), and anti-CD206 (19.”
BackgroundResultInducible antibacterial responses in macrophages
Sweet, M. J., Ramnath, D., Singhal, A., & Kapétanovic, R. (2024) · Nature reviews. Immunology · doi:10.1038/s41577-024-01080-y · Cited by 163 · see citing works
“Alveolar macrophages are ‘gatekeepers’ that orchestrate antimicrobial defence in the lung, having increased phagocytic and antimicrobial capacity compared with interstitial macrophages 171–173 .”
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Boorsma, C. E., Draijer, C., & Melgert, B. N. (2013) · Mediators of Inflammation · doi:10.1155/2013/769214 · Cited by 146 · see citing works
“…phenotypes have been described, what their known functions are, what is known about their presence in the different obstructive and restrictive respiratory diseases (asthma, COPD, pulmonary fibrosis), and how they are thought to contribute to the etiology and resolution of these diseases.”
BackgroundAlcohol's Effects on Lung Health and Immunity
Simet, S. M. (2015) · Alcohol research · doi:10.35946/arcr.v37.2.05 · Cited by 153 · see citing works
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5-Lipoxygenase Reaction Products Modulate Alveolar Macrophage Phagocytosis ofKlebsiella pneumoniae
Mancuso, P., Standiford, T. J., Marshall, T. M., et al. (1998) · Infection and Immunity · doi:10.1128/iai.66.11.5140-5146.1998 · Cited by 134 · see citing works
Alveolar and lung interstitial macrophages: Definitions, functions, and roles in lung fibrosis
Shi, T., Denney, L., An, H., Ho, L., & Zheng, Y. (2020) · Journal of Leukocyte Biology · doi:10.1002/jlb.3ru0720-418r · Cited by 134 · see citing works
Kosyreva, A. M., Dzhalilova, D. S., Lokhonina, А. V., Vishnyakova, P., & Fatkhudinov, T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.682871 · Cited by 120 · see citing works
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“6 4 The activated macrophages would then secrete reactive oxygen species, nitric oxides, and inflammatory cytokines, with the alveolar macrophages secreting more of the radical molecules and TNF and the interstit ial macrophages releasing more of the inflammatory cytokines Il-1 and IL-6.(65) ROS attack on membrane lip…”
BackgroundMathematical model of a three-stage innate immune response to a pneumococcal lung infection
Smith, A. M., McCullers, J. A., & Adler, F. R. (2011) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2011.01.052 · Cited by 118 · see citing works
“…of Theoretical Biology 0022-5193/$ -see front matter Published by Elsevier Ltd. doi:10.1016/j.jtbi.2011.01.052 terminal bronchioles and alveoli (Franke-Ullmann et al., 1996; Jonsson et al., 1985), and coordinate the innate immune response to infection (Kadioglu and Andrew, 2004; Knapp et al.,…”
BackgroundInfluentialMorphological aspects of particle uptake by lung phagocytes
Geiser, M. (2002) · Microscopy Research and Technique · doi:10.1002/jemt.10105 · Cited by 108 · see citing works
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BackgroundThe role of the macrophage in lung disease mediated by bacteria
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BackgroundHoppstädter, J., Diesel, B., Zarbock, R., Breinig, T., Monz, D., Koch, M., Meyerhans, A., Gortner, L., Lehr, C., Huwer, H., et al. (2010) · Respiratory Research · doi:10.1186/1465-9921-11-124 · Cited by 100 · see citing works
“These findings clearly underline the anti-inflammatory phenotype of IM previously described in the literature based on data obtained from murine or rat MF [4,5,9,24].”
BackgroundLung Macrophage Functional Properties in Chronic Obstructive Pulmonary Disease
Akata, K., & van Eeden, S. F. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21030853 · Cited by 91 · see citing works
Dysregulated Functions of Lung Macrophage Populations in COPD
Kapellos, T. S., Bassler, K. E., Aschenbrenner, A. C., Fujii, W., & Schultze, J. L. (2018) · Journal of Immunology Research · doi:10.1155/2018/2349045 · Cited by 85 · see citing works
“Moreover, in mice, they seem to proliferate more than AMs [17].”
BackgroundPickett, T. E., Pasetti, M. F., Galen, J. E., et al. (2000) · Infection and Immunity · doi:10.1128/iai.68.1.205-213.2000 · Cited by 82 · see citing works
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BackgroundPatel, V., Sitapara, R. A., Gore, A., Phan, B. D., Sharma, L., Sampat, V., Li, J. H., Yang, H., Chavan, S. S., Wang, H., et al. (2013) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2012-0279oc · Cited by 81 · see citing works
Abernathy, L., Fountain, M. D., Rothstein, S., David, J. M., Yunker, C. K., Rakowski, J., Lonardo, F., Joiner, M., & Hillman, G. (2015) · Journal of Thoracic Oncology · doi:10.1097/jto.0000000000000677 · Cited by 66 · see citing works
Li, Q., Cheng, Y., Zhang, Z., Bi, Z., Ma, X., Wei, Y., & Wei, X. (2022) · Clinical and Translational Medicine · doi:10.1002/ctm2.1036 · Cited by 77 · see citing works
Pathogenesis of Diffuse Alveolar Hemorrhage in Murine Lupus
Zhuang, H., Han, S., Lee, P. Y., Khaybullin, R. N., Shumyak, S. P., Lu, L., Chatha, A., Afaneh, A. B., Zhang, Y., Xie, C., et al. (2017) · Arthritis & Rheumatology · doi:10.1002/art.40077 · Cited by 78 · see citing works
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BackgroundZhang, Y., Liu, G., Dull, R. O., Schwartz, D. E., & Hu, H. (2014) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00083.2014 · Cited by 71 · see citing works
“144 Isolation of lung interstitial macrophages: The lung after BAL was used for preparation of 145 interstitial macrophages (8).”
MethodAntigen Presentation in the Lung
Kawasaki, T., Ikegawa, M., & Kawai, T. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.860915 · Cited by 73 · see citing works
An Overview of Reactive Oxygen Species
Gilbert, D. L., & Colton, C. A. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/0-306-46806-9_28 · Cited by 69 · see citing works
Gu, Y., Lawrence, T., Mohamed, R., Liang, Y., & Yahaya, B. H. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.923235 · Cited by 68 · see citing works
Li, S., Ni, Z., Cong, B., et al. (2007) · Shock · doi:10.1097/shk.0b013e3180ze26dd · Cited by 66 · see citing works
Yin, B., Chan, C. K. W., Liu, S., Hong, H., Wong, S. H. D., Lee, L. K. C., Ho, L. W. C., Zhang, L., Leung, K. C., Choi, P. C., et al. (2019) · ACS Nano · doi:10.1021/acsnano.9b06424 · Cited by 61 · see citing works
Stokes, R. W., Thorson, L., & Speert, D. P. (1998) · The Journal of Immunology · doi:10.4049/jimmunol.160.11.5514 · Cited by 61 · see citing works
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BackgroundKorcheva, V., Wong, J. W., Lindauer, M., Jacoby, D. B., Iordanov, M. S., & Magun, B. E. (2007) · Molecular Immunology · doi:10.1016/j.molimm.2006.10.025 · Cited by 60 · see citing works
“For example, the secretion of IL-1 and IL-6 in response to LPS has been shown to differ between pulmonary interstitital macrophages and AM [39].”
BackgroundOsorio, F., Lambrecht, B. N., & Janssens, S. (2013) · Seminars in Immunopathology · doi:10.1007/s00281-013-0368-6 · Cited by 59 · see citing works
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Nasrollahi, H., Talepoor, A. G., Saleh, Z., Vakili, M. E., Heydarinezhad, P., Karami, N., Noroozi, M., Meri, S., & Kalantar, K. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1077236 · Cited by 62 · see citing works
“Under steady-state, two distinct populations of macrophages, the interstitial macrophages (IMs) and alveolar macrophages (AMs), are present in the lungs (48, 49).”
BackgroundPneumonia models and innate immunity to respiratory bacterial pathogens
Knapp, S., Schultz, M. J., & Poll, T. V. D. (2005) · Shock · doi:10.1097/01.shk.0000191385.41689.f3 · Cited by 56 · see citing works
“In addition, AMs can also secrete a large range of inflammatory mediators that act directly on the respiratory pathogens or exert indirect effects by recruiting and activating PMNs (1, 3, 4).”
BackgroundOkamoto, M., Tsukamoto, H., Kouwaki, T., Seya, T., & Oshiumi, H. (2017) · Viral Immunology · doi:10.1089/vim.2016.0178 · Cited by 57 · see citing works
“Bronchial macrophages are isolated from induced sputum, and interstitial macrophages are localized in the interstitium (32).”
Draijer, C., Penke, L. R. K., & Peters-Golden, M. L. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1801387 · Cited by 54 · see citing works
“IMs are characterized by high expression of integrin aM (CD11b) and Cx3c chemokine receptor 1 (Cx3cr1) (11, 16, 18, 19).”
BackgroundEruslanov, E. B., Majorov, K. B., ORLOVA, M. O., MISCHENKO, V. V., Kondratieva, T. K., Apt, A. S., & Lyadova, I. V. (2003) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2004.02328.x · Cited by 55 · see citing works
Koudstaal, T., Boomars, K. A., & Kool, M. (2020) · Journal of Clinical Medicine · doi:10.3390/jcm9020561 · Cited by 54 · see citing works
Hoffmann, J., Machado, D., Terrier, O., Pouzol, S., Messaoudi, M., Basualdo, W., Espínola, E. E., Guillen, R. M., Rosa-Calatrava, M., Picot, V., et al. (2016) · Scientific Reports · doi:10.1038/srep38532 · Cited by 53 · see citing works
“With airway epithelial cells 19 , resident alveolar macrophages (AMs) and blood monocytes-derived macrophages (recruited into tissues under inflammatory conditions 20, 21 ) represent a major line of defense against both pneumococcal (through their high phagocytic capacity [22] [23] [24] ) and influenza infection 25, 2…”
BackgroundSteinmüller, C., Franke-Ullmann, G., Lohmann‐Matthes, M., et al. (2000) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/ajrcmb.22.4.3336 · Cited by 53 · see citing works
“However, the percentage of AM contaminations in IM preparations obtained by similar methods in the rat and mouse system was below 5% (8), which is not sufficient to explain the functional heterogeneity between the two macrophage populations.”
BackgroundMethodResultInfluentialSelf-citationIncreased Numbers of Dendritic Cells in the Bronchiolar Tissues of Diffuse Panbronchiolitis
Todate, A., Chida, K., Suda, T., Imokawa, S., Sato, J., Ide, K., Tsuchiya, T., Inui, N., Nakamura, Y., Asada, K., et al. (2000) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.162.1.9907015 · Cited by 52 · see citing works
Earliest Innate Immune Responses Require Macrophage RelA during Pneumococcal Pneumonia
Pittet, L. A., Quinton, L. J., Yamamoto, K., Robson, B. E., Ferrari, J. D., Algül, H., Schmid, R. M., & Mizgerd, J. P. (2011) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2010-0210oc · Cited by 50 · see citing works
Sitapara, R. A., Antoine, D. J., Sharma, L., Patel, V., Ashby, C. R., Gorasiya, S., Yang, H., Zur, M., & Mantell, L. L. (2014) · Molecular Medicine · doi:10.2119/molmed.2013.00086 · Cited by 49 · see citing works
“Alveolar macrophages are the first line of defense against invading pathogens and are the earliest effectors of the phagocytic response against microbial infections in the distal airways (5).”
BackgroundRetractedLee, S.-C., Jaffar, Z. H., Wan, K.-S., Holgate, S. T., & Roberts, K. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.11.6867 · Cited by 49 · see citing works
Ulett, G. C., & Adderson, E. E. (2006) · Current Immunology Reviews · doi:10.2174/157339506776843033 · Cited by 46 · see citing works
“Therefore, the proficiency of the antibacterial function of newborns’ alveolar macrophages [249-251] is considered a crucial component of early immune responses against GBS [252].”
BackgroundOrigin and production of inflammatory perivascular macrophages in pulmonary hypertension
Florentin, J., & Dutta, P. (2017) · Cytokine · doi:10.1016/j.cyto.2017.08.015 · Cited by 44 · see citing works
“Besides fibrosis, interstitial and alveolar macrophages play a major role in lung inflammation[52] and function [52–56].”
BackgroundHaberzettl, P., Duffin, R., Krämer, U., Höhr, D., Schins, R. P. F., Borm, P. J. A., & Albrecht, C. (2007) · Archives of Toxicology · doi:10.1007/s00204-007-0178-5 · Cited by 44 · see citing works
“In this context, a lower phagocytosis capacity of yeast (S. cerevisiae) has been described for IM compared to AM (Franke-Ullmann et al. 1996).”
Aerobiology and Inhalation Exposure to Biological Select Agents and Toxins
Roy, C. J., Reed, D. S., & Hutt, J. A. (2010) · Veterinary Pathology · doi:10.1177/0300985810378650 · Cited by 42 · see citing works
“Some evidence suggests, however, that they may in fact act like other macrophages as professional antigen-presenting cells.(18,33) Interstitial DCs are found throughout the lungs and upper respiratory tract.”
BackgroundInnate Immune Components That Regulate the Pathogenesis and Resolution of hRSV and hMPV Infections
Andrade, C. A., Pacheco, G. A., Gálvez, N. M. S., Soto, J. A., Bueno, S. M., & Kalergis, A. M. (2020) · Viruses · doi:10.3390/v12060637 · Cited by 42 · see citing works
“Macrophages are within the first cells that protect the host against the viral infection, and there are two types in the lungs: the alveolar macrophages (AMs) and the interstitial macrophages (IMs) [138].”
BackgroundToussaint, M., Fiévez, L., Drion, P. V., Cataldo, D. D., Bureau, F., Lekeux, P. M., & Desmet, C. J. (2012) · Mucosal Immunology · doi:10.1038/mi.2012.88 · Cited by 39 · see citing works
MiR-27-3pregulates TLR2/4-dependent mouse alveolar macrophage activation by targetting PPARγ
Wang, D., He, S., Liu, B., & Liu, C. (2018) · Clinical Science · doi:10.1042/cs20180083 · Cited by 39 · see citing works
The Notch ligand DNER regulates macrophage IFNγ release in chronic obstructive pulmonary disease
Ballester‐López, C., Conlon, T. M., Ertüz, Z., Greiffo, F. R., Irmler, M., Verleden, S. E., Beckers, J., Fernandez, I. E., Eickelberg, O., & Yildirim, A. Ö. (2019) · EBioMedicine · doi:10.1016/j.ebiom.2019.03.054 · Cited by 38 · see citing works
“The predominance and contribution of different macrophage subpopulations to the immunopathogenesis of COPD is unclear, especially given the complexity and diversity that entails themacrophage population [34,35].”
BackgroundStolberg, V. R., McCubbrey, A. L., Freeman, C. M., Brown, J. P., Crudgington, S., Taitano, S. H., Saxton, B. L., Mancuso, P., & Curtis, J. L. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402217 · Cited by 39 · see citing works
Emerging role of macrophages in non-infectious diseases: An update
Yousaf, H., Khan, M. I. U., Ali, I., Munir, M. U., & Lee, K. Y. (2023) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2023.114426 · Cited by 35 · see citing works
Delayed neonatal lung macrophage differentiation in a mouse model of in utero ethanol exposure
Gauthier, T. W., Ping, X., Gabelaia, L., et al. (2010) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.90609.2008 · Cited by 34 · see citing works
“This heterogeneity results in a population of cells with variable immune function (15).”
BackgroundGrodzki, A. C., Giulivi, C., & Lein, P. J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054926 · Cited by 34 · see citing works
“In contrast, there are numerous reports that alveolar macrophages have greater functional activity related to antimicrobial defense, including phagocytosis, compared to interstitial macrophages which display enhanced capabilities relevant to specific immune responses such as antigen processing as well as in antioxidan…”
BackgroundBottemanne, P., Paquot, A., Ameraoui, H., et al. (2021) · The FASEB Journal · doi:10.1096/fj.202002555r · Cited by 31 · see citing works
Clinical Management of Complicated Urinary Tract Infection
Nikibakhsh, A. (2011) · InTech eBooks · doi:10.5772/894 · Cited by 30 · see citing works
Wang, M., Gorasiya, S., Antoine, D. J., Sitapara, R. A., Wu, W., Sharma, L., Yang, H., Ashby, C. R., Vasudevan, D., Zur, M., et al. (2014) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2013-0544oc · Cited by 29 · see citing works
Warheit-Niemi, H. I., Hult, E. M., & Moore, B. B. (2019) · Clinical & Translational Immunology · doi:10.1002/cti2.1065 · Cited by 29 · see citing works
“reactive oxygen intermediates, nitric oxide (NO), TNF-a and interferons following stimulation.(71) Macrophages also contribute to immune responses by releasing IL-1 and IL-6, and by upregulating MHC molecules to more efficiently present antigen to recruited lymphocytes.”
BackgroundPlasticity towards Rigidity: A Macrophage Conundrum in Pulmonary Fibrosis
Sari, E., He, C., & Margaroli, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms231911443 · Cited by 26 · see citing works
Silva, M. A., & Berčík, P. (2012) · Laboratory Investigation · doi:10.1038/labinvest.2012.15 · Cited by 27 · see citing works
Ahn, J., Park, J., Kim, D., Lee, T., Jung, D., Kim, Y.-J., Lee, Y., Lee, Y., Seo, I.-S., Song, E., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.738070 · Cited by 24 · see citing works
“(D) AMs were incubated with MAB (MOI 1:25) and indicated reagents (2 h pretreated, L-NAME 1 mM, rIFN-b 1,000 units/ml).”
BackgroundInfluentialMitochondrial Regulation of Inflammasome Activation in Chronic Obstructive Pulmonary Disease
Yoon, C. M., Nam, M., Oh, Y., Cruz, C. S. D., & Kang, M. (2015) · Journal of Innate Immunity · doi:10.1159/000441299 · Cited by 23 · see citing works
Choi, I., Collisson, E. W., Maheswaran, S. K., et al. (2002) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2002.tb00612.x · Cited by 23 · see citing works
“Pig and mouse alveolar macrophages are known to have potent phagocytic abilities and to be good sources of cytokine production, including IL-1, TNF-K, and IFN-Q [5,26,27].”
BackgroundCovin, R. B., Brock, T. G., Bailie, M. B., et al. (1998) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.1998.275.2.l303 · Cited by 23 · see citing works
Phenotypic and Functional Heterogeneity of Low-Density and High-Density Human Lung Macrophages
Balestrieri, B., Granata, F., Loffredo, S., Petraroli, A., Scalia, G., Morabito, P., Cardamone, C., Varricchi, G., & Triggiani, M. (2021) · Biomedicines · doi:10.3390/biomedicines9050505 · Cited by 22 · see citing works
“Differences in morphology, phenotype and function between alveolar and interstitial macrophages in rodents [42,43] and in humans [22,27] have been reported.”
BackgroundBarman, T. K., Racine, R., Bonin, J. L., Califano, D., Salmon, S. L., & Metzger, D. W. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009405 · Cited by 22 · see citing works
Heterogeneity of Lung Mononuclear Phagocytes in Chronic Obstructive Pulmonary Disease
Lee, J. S. (2012) · Journal of Innate Immunity · doi:10.1159/000337434 · Cited by 21 · see citing works
Rodriguez-Rodriguez, L., Gillet, L., & Machiels, B. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1149015 · Cited by 19 · see citing works
Melo, M. D., & Stokes, R. W. (2000) · Tubercle and Lung Disease · doi:10.1054/tuld.1999.0228 · Cited by 19 · see citing works
In situ immune responses to interstitial pneumonitis in human visceral leishmaniasis
Tuon, F. F., Guedes, F., Fernandes, E. R., Pagliari, C., Amato, V. S., & Duarte, M. I. S. (2008) · Parasite Immunology · doi:10.1111/j.1365-3024.2008.01080.x · Cited by 18 · see citing works
McCubbrey, A. L., Barthel, L., Mould, K. J., Mohning, M. P., Redente, E. F., & Janssen, W. J. (2016) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00141.2016 · Cited by 17 · see citing works
Li, M., Li, J., Wang, Y., Jiang, G., Jiang, H., Li, M., Zhu, Z., Ren, F., Wang, Y., Yan, M., et al. (2024) · Stem Cell Research & Therapy · doi:10.1186/s13287-024-04091-7 · Cited by 17 · see citing works
Sul, O., Choi, H. W., Oh, J., & Won, S. H. (2023) · Food and Chemical Toxicology · doi:10.1016/j.fct.2023.113795 · Cited by 17 · see citing works
Apoptosis signal-regulating kinase-1 promotes inflammasome priming in macrophages
Immanuel, C. N., Teng, B., Dong, B. E., Gordon, E. M., Kennedy, J. A., Luellen, C. L., Schwingshackl, A., Cormier, S. A., Fitzpatrick, E. A., & Waters, C. M. (2019) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00199.2018 · Cited by 15 · see citing works
“Macrophages were isolated by consecutive bronchoalveolar lavage as previously described (7, 43, 52, 55) with some minor modifications indicated below.”
MethodSitapara, R. A., Gauthier, A. G., Patel, V., Lin, M., Zur, M., Ashby, C. R., & Mantell, L. L. (2020) · Molecular Medicine · doi:10.1186/s10020-020-00224-9 · Cited by 19 · see citing works
Harpur, C. M., Page, M. A. L., & Tate, M. D. (2021) · Virulence · doi:10.1080/21505594.2021.1939608 · Cited by 16 · see citing works
“IM can be distinguished from AM by their lack of CD11c expression [79] and are generally less phagocytic but more effective at stimulating T cell proliferation [77,80].”
BackgroundLineage tracing reveals the origins and dynamics of macrophages in lung injury and repair
Jin, H., Mou, J., Zhu, H., Liu, K., Zhang, M., Zhang, Z., Pflanz, S., Kasmi, K. E., Liu, Z., Ginhoux, F., et al. (2026) · Cell Discovery · doi:10.1038/s41421-025-00859-0 · Cited by 16 · see citing works
“In contrast, IMs are predominantly found in the lung parenchyma and express high levels of CD11b 16,18 .”
Neuroendocrine and immune interactions with airway macrophages
James, D., & Nijkamp, F. P. (2000) · Inflammation Research · doi:10.1007/pl00000205 · Cited by 13 · see citing works
Yang, S., Zeng, J., Hao, W., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612557 · Cited by 12 · see citing works
- Authors
- Franke-Ullmann, G., Pförtner, C., Walter, P., Steinmüller, C., Lohmann-Matthes, M. L., & Kobzik, L.
- Affiliations
- Fraunhofer Institute for Toxicology and Experimental Medicine (DE)
- ORCID
- Kobzik, L
- Venue
- The Journal of Immunology
- Publisher
- Oxford University Press (OUP)
- Published
- 1996-10-01
- Volume
- 157
- Issue
- 7
- Pages
- 3097-3104
- ISSN
- 0022-1767 (ISSN-L)
- 1550-6606
- OpenAlex
- W1539936851
- Cited by
- 160
- References
- 0
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 6 · 2023: 7 · 2022: 7 · 2021: 12 · 2020: 8 · 2019: 7 · 2018: 7 · 2017: 4 · 2016: 8 · 2015: 10 · 2014: 7 · 2013: 12 · 2012: 5
- FWCI
- 0.69
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Immunology (publishedVersion)
- PubMed (publishedVersion)
- Fraunhofer-Publica (Fraunhofer-Gesellschaft) (submittedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- interstitial macrophages, alveolar macrophages, lung macrophages, phagocytosis, microbicidal activity, reactive oxygen radicals, nitric oxide, TNF-α, interferon, immunoregulatory cytokines, MHC class II, accessory cells, lymphocyte proliferation, innate immunity, adaptive immunity, mouse lung
- MeSH terms
- Interleukin-6 Inhibitors, Animals, Antigen-Presenting Cells, Cells, Cultured, Female, Interferons, Interleukin-1, L Cells, Leishmania donovani, Lung, Macrophage Activation, Macrophages, Mice, Inbred BALB C, Phagocytosis, Mast-Cell Sarcoma, Tumor Cells, Cultured, Tumor Necrosis Factor-alpha, Interleukin-6, Macrophages, Alveolar, Reactive Oxygen Species, Mice
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