Two distinct interstitial macrophage populations coexist across tissues in specific subtissular niches
Abstract
Tissue macrophages have a split personality: Resident tissue macrophages (RTMs) reside in various tissue-specific niches during development. They evince microenvironment-directed phenotypes that support host defense and tissue homeostasis. Chakarov et al. used single-cell RNA sequencing and fate-mapping of murine lung RTMs to interrogate RTM-subset heterogeneity, interrelationships, and ontogeny (see the Perspective by Mildner and Yona). In addition to alveolar macrophages, they identified two different interstitial macrophage populations. One population mostly abutted nerve fibers; the other population preferentially localized near blood vessels and appeared to support vessel integrity and inhibit inflammatory cell infiltration into tissues. Science , this issue p. eaau0964 ; see also p. 1154
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
CX3CR1 is also a marker of lung interstitial macrophages.
“Since CX3CR1 is a marker of the monocyte-to-macrophage transition and also of the lung interstitial macrophages 45”
From Nicotinamide phosphoribosyltransferase prompts bleomycin-induced pulmonary fibrosis by driving macrophage M2 polarization in mice (2024) · cites this paper as [45]
A subset of tissue-resident macrophages co-expresses Lyve1, Fcna, and Cd38.
“Recent reports have characterized gene expression in tissue-resident immune cells and found that Lyve1 and Fcna are expressed along with Cd38 by a subset of tissue-resident macrophages37,38”
From Senescent cells promote tissue NAD+ decline during ageing via the activation of CD38+ macrophages (2020) · cites this paper as [37]
Macrophage-derived amphiregulin induces the differentiation of mesenchymal stromal cells into myofibroblasts via integrin αv-mediated activation of TGF-β.
“macrophage-derived amphiregulin (an epidermal growth factor receptor ligand) has recently been shown to induce the differentiation of mesenchymal stromal cells into myofibroblasts via integrin αv-mediated activation of TGF-β79.”
From Fibrosis: from mechanisms to medicines (2020) · cites this paper as [79]
Cites
Lamb, J., Crawford, E. D., Peck, D., Modell, J. W., Blat, I. C., Wrobel, M. J., Lerner, J., Brunet, J.-P., Subramanian, A., Ross, K. N., et al. (2006) · Science · doi:10.1126/science.1132939 · Cited by 5,257 · see citing works
Fate Mapping Analysis Reveals That Adult Microglia Derive from Primitive Macrophages
Ginhoux, F., Greter, M., Leboeuf, M., Nandi, S., See, P., Gokhan, S., Mehler, M. F., Conway, S. J., Ng, L. G., Stanley, E. R., et al. (2010) · Science · doi:10.1126/science.1194637 · Cited by 5,175 · see citing works
Self-citationMacrophage biology in development, homeostasis and disease
Wynn, T. A., Chawla, A., & Pollard, J. W. (2013) · Nature · doi:10.1038/nature12034 · Cited by 4,684 · cited 1× · see citing works
“Althoughmonocytes and tissue-resident macrophages are involved in the processes of inflammation and tissue repair during fibrosis (57, 58), a role for MRTMs or MRTM subpopulations has not been investigated in suchmodels.”
BackgroundFull-length RNA-seq from single cells using Smart-seq2
Picelli, S., Faridani, O. R., Björklund, Å. K., Winberg, G., Sagasser, S., & Sandberg, R. (2014) · Nature Protocols · doi:10.1038/nprot.2014.006 · Cited by 4,137 · see citing works
Fate Mapping Reveals Origins and Dynamics of Monocytes and Tissue Macrophages under Homeostasis
Yona, S., Kim, K.-W., Wolf, Y., Mildner, A., Varol, D., Breker, M., Strauss-Ayali, D., Viukov, S., Guilliams, M., Misharin, A., et al. (2013) · Immunity · doi:10.1016/j.immuni.2012.12.001 · Cited by 3,245 · see citing works
Self-citationJung, 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
A Lineage of Myeloid Cells Independent of Myb and Hematopoietic Stem Cells
Schulz, C., Perdiguero, E. G., Chorro, L., Szabo-Rogers, H., Cagnard, N., Kierdorf, K., Prinz, M., Wu, B., Jacobsen, S. E. W., Pollard, J. W., et al. (2012) · Science · doi:10.1126/science.1219179 · Cited by 2,578 · see citing works
Smart-seq2 for sensitive full-length transcriptome profiling in single cells
Picelli, S., Björklund, Å. K., Faridani, O. R., Sagasser, S., Winberg, G., & Sandberg, R. (2013) · Nature Methods · doi:10.1038/nmeth.2639 · Cited by 2,358 · see citing works
Hashimoto, D., Chow, A., Noizat, C., Teo, P., Beasley, M. B., Leboeuf, M., Becker, C. D., See, P., Price, J., Lucas, D., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.04.004 · Cited by 2,311 · see citing works
Self-citationTissue-Resident Macrophage Enhancer Landscapes Are Shaped by the Local Microenvironment
Lavin, Y., Winter, D., Blecher-Gonen, R., David, E., Keren-Shaul, H., Merad, M., Jung, S., & Amit, I. (2014) · Cell · doi:10.1016/j.cell.2014.11.018 · Cited by 2,167 · see citing works
the Immunological Genome Consortium, Gautier, E. L., Shay, T., Miller, J., Greter, M., Jakubzick, C., Ivanov, S., Helft, J., Chow, A., Elpek, K. G., et al. (2012) · Nature Immunology · doi:10.1038/ni.2419 · Cited by 1,972 · cited 2× · see citing works
“Of these, tissue of residence is the major contributor, with the ability to almost completely reprogram ontogenically defined identity (29, 30, 51, 52).”
BackgroundTissue-Resident Macrophage Ontogeny and Homeostasis
Ginhoux, F., & Guilliams, M. (2016) · Immunity · doi:10.1016/j.immuni.2016.02.024 · Cited by 1,884 · see citing works
Self-citationPhenotype molding of stromal cells in the lung tumor microenvironment
Lambrechts, D., Wauters, E., Boeckx, B., Aibar, S., Nittner, D., Burton, O., Bassez, A., Decaluwé, H., Pircher, A., Van den Eynde, K., et al. (2018) · Nature Medicine · doi:10.1038/s41591-018-0096-5 · Cited by 1,648 · see citing works
Mapping the Mouse Cell Atlas by Microwell-Seq
Han, X., Wang, R., Zhou, Y., Fei, L., Sun, H., Lai, S., Saadatpour, A., Zhou, Z., Chen, H., Ye, F., et al. (2018) · Cell · doi:10.1016/j.cell.2018.02.001 · Cited by 1,597 · see citing works
LYVE-1, a New Homologue of the CD44 Glycoprotein, Is a Lymph-specific Receptor for Hyaluronan
Banerji, S., Ni, J., Wang, S.-X., Clasper, S., Su, J. Y., Tammi, R., Jones, M., & Jackson, D. G. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.144.4.789 · Cited by 1,586 · see citing works
Epelman, S., Lavine, K. J., Beaudin, A. E., Sojka, D. K., Carrero, J. A., Calderon, B., Brija, T., Gautier, E. L., Ivanov, S., Satpathy, A. T., et al. (2014) · Immunity · doi:10.1016/j.immuni.2013.11.019 · Cited by 1,494 · see citing works
Gosselin, D., Link, V. M., Romanoski, C. E., Fonseca, G. J., Eichenfield, D. Z., Spann, N. J., Stender, J. D., Chun, H. B., Garner, H., Geissmann, F., et al. (2014) · Cell · doi:10.1016/j.cell.2014.11.023 · Cited by 1,307 · see citing works
Ephrin-B2 controls VEGF-induced angiogenesis and lymphangiogenesis
Wang, Y., Nakayama, M., Pitulescu, M. E., Schmidt, T., Bochenek, M. L., Sakakibara, A., Adams, S., Davy, A., Deutsch, U., Lüthi, U., et al. (2010) · Nature · doi:10.1038/nature09002 · Cited by 1,276 · see citing works
Guilliams, M., de Kleer, I., Henri, S., Post, S., Vanhoutte, L., Prijck, S. D., Deswarte, K., MALISSEN, B., Hammad, H., & Lambrecht, B. N. (2013) · The Journal of Experimental Medicine · doi:10.1084/jem.20131199 · Cited by 1,259 · see citing works
Self-citationFate of the mammalian cardiac neural crest
Jiang, X., Rowitch, D. H., Soriano, P. M., McMahon, A. P., & Sucov, H. M. (2000) · Development · doi:10.1242/dev.127.8.1607 · Cited by 1,163 · see citing works
High-efficiency deleter mice show that FLPe is an alternative to Cre-loxP
Rodríguez, C. I., Buchholz, F., Galloway, J. L., Sequerra, R., Kasper, J. S., Ayala, R., Stewart, A. F., & Dymecki, S. M. (2000) · Nature Genetics · doi:10.1038/75973 · Cited by 1,162 · see citing works
Hoeffel, G., Chen, J., Lavin, Y., Low, D., Almeida, F. F., See, P., Beaudin, A. E., Lum, J., Low, I., Forsberg, E. C., et al. (2015) · Immunity · doi:10.1016/j.immuni.2015.03.011 · Cited by 1,135 · cited 4× · see citing works
“In adult S100a4-Rosa mice, all bone marrow (BM) hematopoietic cells, including monocytes, are 100%enhanced yellow fluorescent protein (EYFP)– labeled (4).”
BackgroundMethodInfluentialSelf-citationFUNDAMENTALS OF PLANARIAN REGENERATION
Reddien, P. W., & Alvarado, A. S. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.095114 · Cited by 1,108 · see citing works
Endothelial-pericyte interactions in angiogenesis
Gerhardt, H., & Betsholtz, C. (2003) · Cell and Tissue Research · doi:10.1007/s00441-003-0745-x · Cited by 1,060 · see citing works
Kissenpfennig, A., Henri, S., Dubois, B., Laplace-Builhé, C., Perrin, P., Romani, N., Tripp, C. H., Douillard, P., Leserman, L., Kaiserlian, D., et al. (2005) · Immunity · doi:10.1016/j.immuni.2005.04.004 · Cited by 1,041 · see citing works
Self-citationMacrophages Facilitate Electrical Conduction in the Heart
Hulsmans, M., Clauss, S., Xiao, L., Aguirre, A. D., King, K. R., Hanley, A., Hucker, W. J., Wülfers, E. M., Seemann, G., Courties, G., et al. (2017) · Cell · doi:10.1016/j.cell.2017.03.050 · Cited by 1,011 · see citing works
Denning, T. L., Wang, Y., Patel, S. R., Williams, I. R., & Pulendran, B. (2007) · Nature Immunology · doi:10.1038/ni1511 · Cited by 995 · see citing works
Self-Renewing Resident Cardiac Macrophages Limit Adverse Remodeling Following Myocardial Infarction
Dick, S. A., Macklin, J. A., Nejat, S., Momen, A., Clemente-Casares, X., Althagafi, M. G., Chen, J., Kantores, C., Hosseinzadeh, S., Aronoff, L., et al. (2019) · Nature Immunology · doi:10.1038/s41590-018-0272-2 · Cited by 883 · see citing works
Self-citationBone marrow-derived monocytes give rise to self-renewing and fully differentiated Kupffer cells
Scott, C. L., Zheng, F., De Baetselier, P., Martens, L., Saeys, Y., De Prijck, S., Lippens, S., Abels, C., Schoonooghe, S., Raes, G., et al. (2016) · Nature Communications · doi:10.1038/ncomms10321 · Cited by 860 · see citing works
Schlitzer, A., McGovern, N. N., Teo, P., Zelante, T., Atarashi, K., Low, D., Ho, A. W. S., See, P., Shin, A., Wasan, P. S., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.04.011 · Cited by 834 · see citing works
Self-citationTamoutounour, S., Guilliams, M., Montanana Sanchis, F., Liu, H., Terhorst, D., Malosse, C., Pollet, E., Ardouin, L., Luche, H., Sanchez, C., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.10.004 · Cited by 783 · see citing works
Self-citationRoth, M. E., Obaidat, A., & Hagenbuch, B. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01724.x · Cited by 764 · see citing works
Haniffa, M. A., Shin, A., Bigley, V., McGovern, N. N., Teo, P., See, P., Wasan, P. S., Wang, X.-N., Malinarich, F., Malleret, B., et al. (2012) · Immunity · doi:10.1016/j.immuni.2012.04.012 · Cited by 726 · see citing works
Self-citationTamai, I., Nezu, J., Uchino, H., Sai, Y., Oku, A., Shimane, M., & Tsuji, A. (2000) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.2000.2922 · Cited by 643 · see citing works
A novel endothelial-specific membrane protein is a marker of cell-cell contacts.
Lampugnani, M. G., Resnati, M., Raiteri, M., Pigott, R., Pisacane, A., Houen, G., Ruco, L., & Dejana, E. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.118.6.1511 · Cited by 632 · see citing works
Satpathy, A. T., Wumesh, K. C., Albring, J. C., Edelson, B. T., Kretzer, N. M., Bhattacharya, D., Murphy, T. L., & MURPHY, K. M. M. (2012) · The Journal of Experimental Medicine · doi:10.1084/jem.20120030 · Cited by 628 · see citing works
Schneider, C., Nobs, S. P., Kurrer, M. O., Rehrauer, H., Thiele, C., & Köpf, M. (2014) · Nature Immunology · doi:10.1038/ni.3005 · Cited by 603 · see citing works
van de Laar, L., Saelens, W., Prijck, S. D., Martens, L., Scott, C. L., Isterdael, G. V., Hoffmann, E., Beyaert, R., Saeys, Y., Lambrecht, B., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.02.017 · Cited by 576 · see citing works
Schlitzer, A., Vijayakumar, S., Chen, J., Sumatoh, H., Schreuder, J., Lum, J., Malleret, B., Zhang, S., Larbi, A., Zolezzi, F., et al. (2015) · Nature Immunology · doi:10.1038/ni.3200 · Cited by 564 · see citing works
Self-citationMeredith, M. M., Liu, K., Darrasse-Jeze, G., Kamphorst, A. O., Schreiber, H. A., Guermonprez, P., Idoyaga, J., Cheong, C., Yao, K.-H., Niec, R. E., et al. (2012) · Journal of Experimental Medicine · doi:10.1084/jem.20112675 · Cited by 524 · see citing works
Pirzgalska, R. M., Seixas, E., Seidman, J. S., Link, V. M., Martínez‐Sánchez, N., Mahú, I., Mendes, R., Gres, V., Kubasova, N., Morris, I., et al. (2017) · Nature Medicine · doi:10.1038/nm.4422 · Cited by 497 · see citing works
Three Unique Interstitial Macrophages in the Murine Lung at Steady State
Gibbings, S. L., Thomas, S. M., Atif, S. M., McCubbrey, A. L., Desch, A. N., Danhorn, T., Leach, S. M., Bratton, D. L., Henson, P. M., Janssen, W. J., et al. (2017) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/rcmb.2016-0361oc · Cited by 476 · see citing works
Pham, T. H. M., Baluk, P., Xu, Y., Grigorova, I., Bankovich, A. J., Pappu, R., Coughlin, S. R., McDonald, D. M., Schwab, S. R., & Cyster, J. G. (2010) · Journal of Experimental Medicine · doi:10.1084/jem.20091619 · Cited by 444 · see citing works
Lung interstitial macrophages alter dendritic cell functions to prevent airway allergy in mice
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
Self-citationAgouti C57BL/6N embryonic stem cells for mouse genetic resources
Pettitt, S. J., Liang, Q., Rairdan, X. Y., Moran, J. L., Prosser, H. M., Beier, D. R., Lloyd, K. C. K., Bradley, A., & Skarnes, W. C. (2009) · Nature Methods · doi:10.1038/nmeth.1342 · Cited by 384 · see citing works
Lim, H. Y., Lim, S. Y., Tan, C. K., Thiam, C. H., Goh, C. C., Carbajo, D., Chew, S. H. S., See, P., Chakarov, S., Wang, X. N., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.06.008 · Cited by 384 · see citing works
Self-citationEnsan, S., Li, A., Besla, R., Degousee, N., Cosme, J., Roufaiel, M., Shikatani, E. A., El-Maklizi, M., Williams, J. W., Robins, L., et al. (2016) · Nature Immunology · doi:10.1038/ni.3343 · Cited by 372 · see citing works
Stabilized imaging of immune surveillance in the mouse lung
Looney, M. R., Thornton, E. E., Sen, D., Lamm, W. J., Glenny, R. W., & Krummel, M. F. (2010) · Nature Methods · doi:10.1038/nmeth.1543 · Cited by 364 · see citing works
Isoproterenol-induced myocardial fibrosis in relation to myocyte necrosis.
Benjamin, I. J., Jalil, J., Tan, L. B., Cho, K., Weber, K. T., & Clark, W. A. (1989) · Circulation Research · doi:10.1161/01.res.65.3.657 · Cited by 343 · see citing works
Self-citationPinto, A. R., Paolicelli, R., Salimova, E., Gospocic, J., Slonimsky, E., Bilbao-Cortes, D., Godwin, J. W., & Rosenthal, N. A. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036814 · Cited by 318 · see citing works
Lim, H. Y., Thiam, C. H., Yeo, K. P., Bisoendial, R. J., Hii, C. S., McGrath, K. C. Y., Tan, K. W., Heather, A. K., Alexander, J. S., & Angeli, V. (2013) · Cell Metabolism · doi:10.1016/j.cmet.2013.04.002 · Cited by 309 · see citing works
Self-citationAngiogenic Role of LYVE-1–Positive Macrophages in Adipose Tissue
Cho, C.-H., Jun Koh, Y., Han, J., Sung, H.-K., Jong Lee, H., Morisada, T., Schwendener, R. A., Brekken, R. A., Kang, G., Oike, Y., et al. (2007) · Circulation Research · doi:10.1161/01.res.0000259564.92792.93 · Cited by 309 · see citing works
Identification of an atypical monocyte and committed progenitor involved in fibrosis
Satoh, T., Nakagawa, K., Sugihara, F., Kuwahara, R., Ashihara, M., Yamane, F., Minowa, Y., Fukushima, K., Ebina, I., Yoshioka, Y., et al. (2017) · Nature · doi:10.1038/nature20611 · Cited by 302 · see citing works
Perivascular macrophages mediate neutrophil recruitment during bacterial skin infection
Abtin, A., Jain, R., Mitchell, A. J., Roediger, B., Brzoska, A. J., Tikoo, S., Cheng, Q., Ng, L. G., Cavanagh, L. L., von Andrian, U. H., et al. (2013) · Nature Immunology · doi:10.1038/ni.2769 · Cited by 291 · see citing works
Self-citationTCR ligand density and affinity determine peripheral induction of Foxp3 in vivo
Gottschalk, R. A., Corse, E., & Allison, J. P. (2010) · The Journal of Experimental Medicine · doi:10.1084/jem.20091999 · Cited by 279 · see citing works
Apoptosis and Expression of Fas/Fas Ligand mRNA in Bleomycin-Induced Pulmonary Fibrosis in Mice
Hagimoto, N., Kuwano, K., Nomoto, Y., Kunitake, R., & Hara, N. (1997) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/ajrcmb.16.1.8998084 · Cited by 273 · see citing works
Brown-adipose-tissue macrophages control tissue innervation and homeostatic energy expenditure
Wolf, Y., Boura‐Halfon, S., Cortese, N., Haimon, Z., Shalom, H. S., Kuperman, Y., Kalchenko, V., Brandis, A. S., David, E., Segal-Hayoun, Y., et al. (2017) · Nature Immunology · doi:10.1038/ni.3746 · Cited by 251 · see citing works
Sabatel, C. M., Radermecker, C., Fiévez, L., Paulissen, G., Chakarov, S., Fernandes, C., Olivier, S., Toussaint, M., Pirottin, D., Xiao, X., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.02.016 · Cited by 231 · see citing works
Self-citationJin, X., Ishii, H., Bai, Z., Itokazu, T., & Yamashita, T. (2012) · PLoS ONE · doi:10.1371/journal.pone.0041892 · Cited by 211 · see citing works
The Role of the Th2 CC Chemokine Ligand CCL17 in Pulmonary Fibrosis
Belperio, J. A., Dy, M. C., Murray, L. A., Burdick, M. D., Xue, Y., Strieter, R. M., & Keane, M. P. (2004) · The Journal of Immunology · doi:10.4049/jimmunol.173.7.4692 · Cited by 174 · see citing works
Hypercholesterolemic Mice Exhibit Lymphatic Vessel Dysfunction and Degeneration
Lim, H. Y., Rutkowski, J. M., Helft, J., Reddy, S. T., Swartz, M. A., Randolph, G. J., & Angeli, V. (2009) · American Journal Of Pathology · doi:10.2353/ajpath.2009.080963 · Cited by 171 · see citing works
Self-citationIshida, Y., Kimura, A., Kondo, T., Hayashi, T., Ueno, M., Takakura, N., Matsushima, K., & Mukaida, N. (2007) · American Journal Of Pathology · doi:10.2353/ajpath.2007.051213 · Cited by 170 · see citing works
LYVE-1–Positive Macrophages Are Present in Normal Murine Eyes
Xu, H., Chen, M., Reid, D. M., & Forrester, J. V. (2007) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.06-0783 · Cited by 132 · see citing works
Koronyo‐Hamaoui, M., Ko, M. K., Koronyo, Y., Azoulay, D., Seksenyan, A., Kunis, G., Pham, M. D., Bakhsheshian, J., Rogeri, P. S., Black, K. L., et al. (2009) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2009.06402.x · Cited by 113 · see citing works
Lee, L. K., Ghorbanian, Y., Wang, W., Wang, Y., Kim, Y. J., Weissman, I. L., Inlay, M. A., & Mikkola, H. K. A. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.10.080 · Cited by 79 · see citing works
Yokoyama, T., Lee, J.-K., Miwa, K., Tobias Opthof, A., Tomoyama, S., Nakanishi, H., Yoshida, A., Yasui, H., Iida, T., Miyagawa, S., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0182072 · Cited by 53 · see citing works
Barreiro, O., Cibrián, D., Clemente, C., Álvarez, D., Moreno, V., Valiente, Í., Bernad, A., Vestweber, D., Arroyo, A. G., Martı́n, P., et al. (2016) · eLife · doi:10.7554/elife.15251 · Cited by 45 · see citing works
Adipose tissue macrophages induce PPARγ-high FOXP3+ regulatory T cells
Onodera, T., Fukuhara, A., Jang, M. H., Shin, J., Aoi, K., Kikuta, J., Otsuki, M., Ishii, M., & Shimomura, I. (2015) · Scientific Reports · doi:10.1038/srep16801 · Cited by 39 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Fibrosis: from mechanisms to medicines
Henderson, N. C., Rieder, F., & Wynn, T. A. (2020) · Nature · doi:10.1038/s41586-020-2938-9 · Cited by 1,868 · see citing works
A pan-cancer single-cell transcriptional atlas of tumor infiltrating myeloid cells
Cheng, S., Li, Z., Gao, R., Xing, B., Gao, Y., Yang, Y., Qin, S., Zhang, L., Ouyang, H., Du, P., et al. (2021) · Cell · doi:10.1016/j.cell.2021.01.010 · Cited by 1,601 · see citing works
Single-Cell Analyses Inform Mechanisms of Myeloid-Targeted Therapies in Colon Cancer
Zhang, L., Li, Z., Skrzypczynska, K. M., Fang, Q., Zhang, W., O’Brien, S. A., He, Y., Wang, L., Zhang, Q., Kim, A., et al. (2020) · Cell · doi:10.1016/j.cell.2020.03.048 · Cited by 1,575 · see citing works
Microglia Biology: One Century of Evolving Concepts
Prinz, M., Jung, S., & Priller, J. (2019) · Cell · doi:10.1016/j.cell.2019.08.053 · Cited by 1,525 · see citing works
Lipid-associated macrophages control metabolic homeostasis in a Trem2-dependent manner
Jaitin, D. A., Adlung, L., Thaiss, C. A., Weiner, A., Li, B., Descamps, H., Lundgren, P., Bleriot, C., Liu, Z., Deczkowska, A., et al. (2019) · Cell · doi:10.1016/j.cell.2019.05.054 · Cited by 1,377 · see citing works
Self-citationGuidelines for the use of flow cytometry and cell sorting in immunological studies (second edition)
Cossarizza, A., Chang, H., Radbruch, A., Acs, A., Adam, D., Adam‐Klages, S., Agace, W. W., Aghaeepour, N., Akdiş, M., Allez, M., et al. (2019) · European Journal of Immunology · doi:10.1002/eji.201970107 · Cited by 982 · see citing works
The role of macrophages in the resolution of inflammation
Watanabe, S., Alexander, M., Misharin, A. V., & Budinger, G. R. S. (2019) · Journal of Clinical Investigation · doi:10.1172/jci124615 · Cited by 925 · see citing works
The immunology of rheumatoid arthritis
Weyand, C. M., & Goronzy, J. J. (2020) · Nature Immunology · doi:10.1038/s41590-020-00816-x · Cited by 821 · see citing works
A pan-cancer blueprint of the heterogeneous tumor microenvironment revealed by single-cell profiling
Qian, J., Olbrecht, S., Boeckx, B., Vos, H., Laoui, D., Etlioglu, E., Wauters, E., Pomella, V., Verbandt, S., Busschaert, P., et al. (2020) · Cell Research · doi:10.1038/s41422-020-0355-0 · Cited by 818 · see citing works
A Network of Macrophages Supports Mitochondrial Homeostasis in the Heart
Nicolás-Ávila, J. A., Lechuga-Vieco, A. V., Esteban-Martínez, L., Sánchez-Díaz, M., Díaz-García, E., Santiago, D. J., Rubio-Ponce, A., Li, J. L., Balachander, A., Quintana, J. A., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.031 · Cited by 762 · see citing works
Self-citationThe pathogenesis of rheumatoid arthritis
Alivernini, S., Firestein, G. S., & McInnes, I. B. (2022) · Immunity · doi:10.1016/j.immuni.2022.11.009 · Cited by 739 · see citing works
Fate Mapping via Ms4a3-Expression History Traces Monocyte-Derived Cells
Liu, Z., Gu, Y., Chakarov, S., Bleriot, C., Kwok, I., Chen, X., Shin, A., Huang, W., Dress, R. J., Dutertre, C.-A., et al. (2019) · Cell · doi:10.1016/j.cell.2019.08.009 · Cited by 719 · see citing works
Self-citationSharma, A., Seow, J. J. W., Dutertre, C.-A., Pai, R., Blériot, C., Mishra, A., Wong, R. M. M., Singh, G. S. N., Sudhagar, S., Khalilnezhad, S., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.040 · Cited by 677 · see citing works
Self-citationCross-tissue single-cell landscape of human monocytes and macrophages in health and disease
Mulder, K., Patel, A. A., Kong, W. T., Piot, C., Halitzki, E., Dunsmore, G., Khalilnezhad, S., Irac, S. E., Dubuisson, A., Chevrier, M., et al. (2021) · Immunity · doi:10.1016/j.immuni.2021.07.007 · Cited by 678 · see citing works
Self-citationCells of the human intestinal tract mapped across space and time
Elmentaite, R., Kumasaka, N., Roberts, K., Fleming, A., Dann, E., King, H. W., Kleshchevnikov, V., Dabrowska, M. H., Pritchard, S., Bolt, L., et al. (2021) · Nature · doi:10.1038/s41586-021-03852-1 · Cited by 677 · see citing works
Macrophages in health and disease
Park, M. D., Silvin, A., Ginhoux, F., & Merad, M. (2022) · Cell · doi:10.1016/j.cell.2022.10.007 · Cited by 644 · see citing works
Self-citationLocally renewing resident synovial macrophages provide a protective barrier for the joint
Culemann, S., Grüneboom, A., Nicolás-Ávila, J. Á., Weidner, D., Lämmle, K. F., Rothe, T., Quintana, J. A., Kirchner, P., Krljanac, B., Eberhardt, M., et al. (2019) · Nature · doi:10.1038/s41586-019-1471-1 · Cited by 634 · see citing works
Biology of lung macrophages in health and disease
Aegerter, H., Lambrecht, B. N., & Jakubzick, C. (2022) · Immunity · doi:10.1016/j.immuni.2022.08.010 · Cited by 628 · see citing works
Tissue-specific macrophages: how they develop and choreograph tissue biology
Mass, E., Nimmerjahn, F., Kierdorf, K., & Schlitzer, A. (2023) · Nature Reviews Immunology · doi:10.1038/s41577-023-00848-y · Cited by 621 · see citing works
Self-citationTissue-resident FOLR2+ macrophages associate with CD8+ T cell infiltration in human breast cancer
Ramos, R. N., Missolo-Koussou, Y., Gerber-Ferder, Y., Bromley, C. P., Bugatti, M., Núñez, N. G., Tosello, J., Richer, W., Menger, L., Denizeau, J., et al. (2022) · Cell · doi:10.1016/j.cell.2022.02.021 · Cited by 595 · see citing works
Self-citationDick, S. A., Wong, A., Hamidzada, H., Nejat, S., Nechanitzky, R., Vohra, S., Mueller, B., Zaman, R., Kantores, C., Aronoff, L., et al. (2022) · Science Immunology · doi:10.1126/sciimmunol.abf7777 · Cited by 538 · see citing works
Guidelines for the use of flow cytometry and cell sorting in immunological studies (third edition)
Cossarizza, A., Chang, H., Radbruch, A., Abrignani, S., Addo, R., Akdis, M., Andrä, I., Andreata, F., Annunziato, F., Arranz, E., et al. (2021) · European Journal of Immunology · doi:10.1002/eji.202170126 · Cited by 531 · see citing works
Self-citationDeterminants of resident tissue macrophage identity and function
Blériot, C., Chakarov, S., & Ginhoux, F. (2020) · Immunity · doi:10.1016/j.immuni.2020.05.014 · Cited by 507 · see citing works
Self-citationFibroblast-macrophage reciprocal interactions in health, fibrosis, and cancer
Buechler, M. B., Fu, W., & Turley, S. J. (2021) · Immunity · doi:10.1016/j.immuni.2021.04.021 · Cited by 494 · see citing works
Single-cell transcriptomics reveals cell-type-specific diversification in human heart failure
Koenig, A. L., Shchukina, I., Amrute, J., Andhey, P. S., Zaitsev, K., Lai, L., Bajpai, G., Bredemeyer, A., Smith, G., Jones, C., et al. (2022) · Nature Cardiovascular Research · doi:10.1038/s44161-022-00028-6 · Cited by 482 · see citing works
Macrophages in Lung Injury, Repair, and Fibrosis
Cheng, P., Li, S., & Chen, H. (2021) · Cells · doi:10.3390/cells10020436 · Cited by 443 · see citing works
Senescent cells promote tissue NAD+ decline during ageing via the activation of CD38+ macrophages
Covarrubias, A. J., Kale, A., Perrone, R., Lopez-Dominguez, J. A., Pisco, A. O., Kasler, H. G., Schmidt, M. S., Heckenbach, I., Kwok, R., Wiley, C. D., et al. (2020) · Nature Metabolism · doi:10.1038/s42255-020-00305-3 · Cited by 420 · see citing works
Role of Cardiac Macrophages on Cardiac Inflammation, Fibrosis and Tissue Repair
Lafuse, W. P., Wozniak, D. J., & Rajaram, M. V. S. (2020) · Cells · doi:10.3390/cells10010051 · Cited by 400 · see citing works
Single-nucleus cross-tissue molecular reference maps toward understanding disease gene function
Eraslan, G., Drokhlyansky, E., Anand, S. K., Fiškin, E., Subramanian, A., Slyper, M., Wang, J., Wittenberghe, N. V., Rouhana, J. M., Waldman, J., et al. (2022) · Science · doi:10.1126/science.abl4290 · Cited by 396 · see citing works
Macrophages in cardiovascular diseases: molecular mechanisms and therapeutic targets
Chen, R., Zhang, H., Tang, B., Luo, Y., Yang, Y., Zhong, X., Chen, S., Xu, X., Huang, S., & Liu, C. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01840-1 · Cited by 387 · see citing works
Inflammation and Skeletal Muscle Regeneration: Leave It to the Macrophages!
Chazaud, B. (2020) · Trends in Immunology · doi:10.1016/j.it.2020.04.006 · Cited by 378 · see citing works
Martin, K. E., & Garcı́a, A. J. (2021) · Acta Biomaterialia · doi:10.1016/j.actbio.2021.03.038 · Cited by 375 · see citing works
Meta-Analysis of Leukocyte Diversity in Atherosclerotic Mouse Aortas
Zernecke, A., Winkels, H., Cochain, C., Williams, J. W., Wolf, D., Soehnlein, O., Robbins, C. S., Monaco, C. G., Park, I., McNamara, C. A., et al. (2020) · Circulation Research · doi:10.1161/circresaha.120.316903 · Cited by 373 · see citing works
Tissue macrophages: origin, heterogenity, biological functions, diseases and therapeutic targets
Guan, F., Wang, R., Yi, Z., Luo, P., Liu, W., Xie, Y., Liu, Z., Xia, Z., Zhang, H., & Cheng, Q. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02124-y · Cited by 371 · see citing works
Rojo, R., Raper, A., Ozdemir, D. D., Lefèvre, L., Grabert, K., Wollscheid-Lengeling, E., Bradford, B. M., Caruso, M., Gažová, I., Sánchez, A., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11053-8 · Cited by 372 · see citing works
Sárvári, A. K., Hauwaert, E. L. V., Markussen, L. K., Gammelmark, E., Marcher, A.-B., Ebbesen, M. F., Nielsen, R., Brewer, J. R., Madsen, J. G. S., & Mandrup, S. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.12.004 · Cited by 368 · see citing works
Roles of macrophages in tumor development: a spatiotemporal perspective
Bied, M., Ho, W. W., Ginhoux, F., & Blériot, C. (2023) · Cellular and Molecular Immunology · doi:10.1038/s41423-023-01061-6 · Cited by 360 · see citing works
Self-citationHildreth, A. D., Ma, F., Wong, Y. Y., Sun, R., Pellegrini, M. A., & O’Sullivan, T. E. (2021) · Nature Immunology · doi:10.1038/s41590-021-00922-4 · Cited by 358 · see citing works
Leader, A. M., Grout, J. A., Maier, B. B., Nabet, B. Y., Park, M. D., Tabachnikova, A., Chang, C., Walker, L. A., Lansky, A., Bérichel, J. L., et al. (2021) · Cancer Cell · doi:10.1016/j.ccell.2021.10.009 · Cited by 356 · see citing works
Joshi, N., Watanabe, S., Verma, R., Jablonski, R. P., Chen, C.-I., Cheresh, P., Markov, N. S., Reyfman, P. A., McQuattie-Pimentel, A. C., Sichizya, L., et al. (2020) · European Respiratory Journal · doi:10.1183/13993003.00646-2019 · Cited by 344 · see citing works
Macrophage phenotypes and functions: resolving inflammation and restoring homeostasis
Rodríguez-Morales, P., & Franklin, R. A. (2023) · Trends in Immunology · doi:10.1016/j.it.2023.10.004 · Cited by 327 · see citing works
Lei, F., Cui, N., Zhou, C., Chodosh, J., Vavvas, D. G., & Paschalis, E. I. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1922788117 · Cited by 322 · see citing works
Schyns, J., Bai, Q., Ruscitti, C., Radermecker, C., Schepper, S. D., Chakarov, S., Farnir, F., Pirottin, D., Ginhoux, F., Boeckxstaens, G. E., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-11843-0 · Cited by 320 · see citing works
Self-citationTissue-resident macrophages in omentum promote metastatic spread of ovarian cancer
Etzerodt, A., Moulin, M., Doktor, T. K., Delfini, M., Mossadegh‐Keller, N., Bajénoff, M., Sieweke, M. H., Moestrup, S. K., Auphan‐Anezin, N., & Lawrence, T. (2020) · The Journal of Experimental Medicine · doi:10.1084/jem.20191869 · Cited by 320 · see citing works
Macrophages in cardiac remodelling after myocardial infarction
Yap, J., Irei, J. S., Lozano-Gerona, J., Vanapruks, S., Bishop, T., & Boisvert, W. A. (2023) · Nature Reviews Cardiology · doi:10.1038/s41569-022-00823-5 · Cited by 316 · see citing works
Gao, Y., Li, J., Cheng, W., Diao, T., Liu, H., Bo, Y., Liu, C., Zhou, W., Chen, M., Zhang, Y., et al. (2024) · Cancer Cell · doi:10.1016/j.ccell.2024.08.020 · Cited by 304 · see citing works
Distinct microbial and immune niches of the human colon
James, K. R., Gomes, T., Elmentaite, R., Kumar, N., Gulliver, E. L., King, H. W., Stares, M. D., Bareham, B. R., Ferdinand, J. R., Petrova, V. N., et al. (2020) · Nature Immunology · doi:10.1038/s41590-020-0602-z · Cited by 301 · see citing works
Timperi, E., Gueguen, P., Molgora, M., Magagna, I., Kieffer, Y., Lopez‐Lastra, S., Sirven, P., Baudrin, L. G., Baulande, S., Nicolas, A., et al. (2022) · Cancer Research · doi:10.1158/0008-5472.can-22-1427 · Cited by 299 · see citing works
Ural, B. B., Yeung, S. T., Damani‐Yokota, P., Devlin, J. C., de Vries, M., Vera‐Licona, P., Samji, T., Sawai, C. M., Jang, G., Perez, O. A., et al. (2020) · Science Immunology · doi:10.1126/sciimmunol.aax8756 · Cited by 281 · see citing works
Song, H., Weinstein, H. N. W., Allegakoen, P., Wadsworth, M. H., Xie, J., Yang, H., Castro, E. A., Lu, K. L., Stohr, B. A., Feng, F. Y.-C., et al. (2022) · Nature Communications · doi:10.1038/s41467-021-27322-4 · Cited by 280 · see citing works
Macrophages, Chronic Inflammation, and Insulin Resistance
He, L., Meng, Y., He, S., Tan, X., Zhang, Y., Zhang, X., Wang, L., & Zheng, W. (2022) · Cells · doi:10.3390/cells11193001 · Cited by 278 · see citing works
Self-citationMucosal immune responses to infection and vaccination in the respiratory tract
Mettelman, R. C., Allen, E. K., & Thomas, P. G. (2022) · Immunity · doi:10.1016/j.immuni.2022.04.013 · Cited by 272 · see citing works
Synovial tissue macrophages in joint homeostasis, rheumatoid arthritis and disease remission
Kurowska‐Stolarska, M., & Alivernini, S. (2022) · Nature Reviews Rheumatology · doi:10.1038/s41584-022-00790-8 · Cited by 272 · see citing works
Macrophage function in adipose tissue homeostasis and metabolic inflammation
Chavakis, T., Alexaki, V. I., & Ferrante, A. W. (2023) · Nature Immunology · doi:10.1038/s41590-023-01479-0 · Cited by 264 · see citing works
Tan, J., Fan, W., Liu, T., Zhu, B., Liu, Y., Wang, S., Wu, J. H., Liu, J., Zou, F., Wei, J., et al. (2023) · Journal of Hepatology · doi:10.1016/j.jhep.2023.02.032 · Cited by 258 · see citing works
Self-citationBain, C. C., & MacDonald, A. S. (2022) · Mucosal Immunology · doi:10.1038/s41385-021-00480-w · Cited by 253 · see citing works
Ydens, E., Amann, L., Asselbergh, B., Scott, C. L., Martens, L., Sichien, D., Mossad, O., Blank, T., Prijck, S. D., Low, D., et al. (2020) · Nature Neuroscience · doi:10.1038/s41593-020-0618-6 · Cited by 243 · see citing works
Self-citationOntogeny of Tumor-Associated Macrophages
Laviron, M., & Boissonnas, A. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01799 · Cited by 241 · see citing works
A subset of Kupffer cells regulates metabolism through the expression of CD36
Blériot, C., Barreby, E., Dunsmore, G., Ballaire, R., Chakarov, S., Ficht, X., De Simone, G., Andreata, F., Fumagalli, V., Guo, W., et al. (2021) · Immunity · doi:10.1016/j.immuni.2021.08.006 · Cited by 236 · see citing works
Self-citationDoes tissue imprinting restrict macrophage plasticity?
Guilliams, M., & Svedberg, F. R. (2021) · Nature Immunology · doi:10.1038/s41590-020-00849-2 · Cited by 232 · see citing works
Krenkel, O., Hundertmark, J., Abdallah, A. T., Kohlhepp, M., Puengel, T., Roth, T., Branco, D. P. P., Mossanen, J. C., Luedde, T., Trautwein, C., et al. (2020) · Gut · doi:10.1136/gutjnl-2019-318382 · Cited by 220 · see citing works
A spatially resolved atlas of the human lung characterizes a gland-associated immune niche
Madissoon, E., Oliver, A. J., Kleshchevnikov, V., Wilbrey-Clark, A., Polanski, K., Richoz, N., Ribeiro Orsi, A., Mamanova, L., Bolt, L., Elmentaite, R., et al. (2023) · Nature Genetics · doi:10.1038/s41588-022-01243-4 · Cited by 219 · see citing works
Human skeletal muscle aging atlas
Kedlian, V. R., Wang, Y., Liu, T., Chen, X., Bolt, L., Tudor, C., Shen, Z., Fasouli, E. S., Prigmore, E., Kleshchevnikov, V., et al. (2024) · Nature Aging · doi:10.1038/s43587-024-00613-3 · Cited by 218 · see citing works
Diversity of Macrophages in Lung Homeostasis and Diseases
Hou, F., Xiao, K., Tang, L., & Xie, L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.753940 · Cited by 216 · see citing works
Inducing trained immunity in pro-metastatic macrophages to control tumor metastasis
Ding, C., Shrestha, R., Zhu, X., Geller, A. E., Wu, S., Woeste, M. R., Li, W., Wang, H., Yuan, F., Xu, R., et al. (2023) · Nature Immunology · doi:10.1038/s41590-022-01388-8 · Cited by 215 · see citing works
Self-citationTan, Y., Flynn, W. F., Sivajothi, S. K., Luo, D., Bozal, S. B., Davé, M., Luciano, A. A., Robson, P., Luciano, D. E., & Courtois, E. T. (2022) · Nature Cell Biology · doi:10.1038/s41556-022-00961-5 · Cited by 211 · see citing works
Adipose tissue at single-cell resolution
Maniyadath, B., Zhang, Q., Gupta, R. K., & Mandrup, S. (2023) · Cell Metabolism · doi:10.1016/j.cmet.2023.02.002 · Cited by 207 · see citing works
The Ontogeny of Monocyte Subsets
Wolf, A. A., Yáñez, A., Barman, P. K., & Goodridge, H. S. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01642 · Cited by 201 · see citing works
Macrophage: A Cell With Many Faces and Functions in Tuberculosis
Ahmad, F., Rani, A., Alam, A., Zarin, S., Pandey, S., Singh, H., Hasnain, S. E., & Ehtesham, N. Z. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.747799 · Cited by 200 · see citing works
Hilgendorf, I., Frantz, S., & Frangogiannis, N. G. (2024) · Circulation Research · doi:10.1161/circresaha.124.323658 · Cited by 200 · see citing works
Single cell analysis of M. tuberculosis phenotype and macrophage lineages in the infected lung
Pisu, D., Huang, L., Narang, V., Theriault, M. E., Lê-Bury, G., Lee, B. T. K., Lakudzala, A. E., Mzinza, D. T., Mhango, D. V., Mitini-Nkhoma, S. C., et al. (2021) · The Journal of Experimental Medicine · doi:10.1084/jem.20210615 · Cited by 193 · see citing works
Wei, J., Chen, P., Gupta, P., Ott, M., Zamler, D. B., Kassab, C., Bhat, K., Curran, M. A., de Groot, J., & Heimberger, A. B. (2019) · Neuro-Oncology · doi:10.1093/neuonc/noz212 · Cited by 192 · see citing works
Andrews, T. S., Nakib, D., Perciani, C. T., Zhong, X. Y., Liu, L. Y., Winter, E., Camat, D., Chung, S., Lumanto, P., Manuel, J., et al. (2024) · Journal of Hepatology · doi:10.1016/j.jhep.2023.12.023 · Cited by 191 · see citing works
Transformer for one stop interpretable cell type annotation
Chen, J., Xu, H., Tao, W., Chen, Z., Zhao, Y., & Han, J.-D. J. (2023) · Nature Communications · doi:10.1038/s41467-023-35923-4 · Cited by 189 · see citing works
Self-citationLiu, Y., Feng, W., Dai, Y., Bao, M., Yuan, Z., He, M., Qin, Z., Liao, S., He, J., Huang, Q., et al. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.709210 · Cited by 184 · see citing works
Distinct developmental pathways from blood monocytes generate human lung macrophage diversity
Evren, E., Ringqvist, E. E., Tripathi, K. P., Sleiers, N., Rives, I. C., Alisjahbana, A., Gao, Y., Sarhan, D., Halle, T., Sorini, C., et al. (2020) · Immunity · doi:10.1016/j.immuni.2020.12.003 · Cited by 183 · see citing works
Spatially Segregated Macrophage Populations Predict Distinct Outcomes in Colon Cancer
Matusiak, M., Hickey, J. W., van IJzendoorn, D. G. P., Lu, G., Kidziński, Ł., Zhu, S., Colburg, D. R. C., Luca, B. A., Phillips, D. J., Brubaker, S. W., et al. (2024) · Cancer Discovery · doi:10.1158/2159-8290.cd-23-1300 · Cited by 184 · see citing works
Reyes, N. S., Krasilnikov, M., Allen, N. C., Lee, J. Y., Hyams, B., Zhou, M., Ravishankar, S., Cassandras, M., Wang, C., Khan, I., et al. (2022) · Science · doi:10.1126/science.abf3326 · Cited by 181 · see citing works
A Binary Cre Transgenic Approach Dissects Microglia and CNS Border-Associated Macrophages
Kim, J.-S., Kolesnikov, M., Peled-Hajaj, S., Scheyltjens, I., Xia, Y., Trzebanski, S., Haimon, Z., Shemer, A., Lubart, A., Van Hove, H., et al. (2021) · Immunity · doi:10.1016/j.immuni.2020.11.007 · Cited by 176 · see citing works
Zheng, X., Wang, X., Cheng, X., Liu, Z., Yin, Y., Li, X., Huang, Z., Wang, Z., Guo, W., Ginhoux, F., et al. (2023) · Nature Cancer · doi:10.1038/s43018-023-00599-8 · Cited by 172 · see citing works
Self-citationTissue-resident macrophages: guardians of organ homeostasis
Nobs, S. P., & Köpf, M. (2021) · Trends in Immunology · doi:10.1016/j.it.2021.04.007 · Cited by 172 · see citing works
Origin and ontogeny of lung macrophages: from mice to humans
Evren, E., Ringqvist, E. E., & Willinger, T. (2019) · Immunology · doi:10.1111/imm.13154 · Cited by 170 · see citing works
Hoyer, F. F., Naxerova, K., Schloss, M. J., Hulsmans, M., Nair, A. V., Dutta, P., Calcagno, D. M., Hérisson, F., Anzai, A., Sun, Y., et al. (2019) · Immunity · doi:10.1016/j.immuni.2019.10.010 · Cited by 169 · see citing works
Tissue-resident ductal macrophages survey the mammary epithelium and facilitate tissue remodelling
Dawson, C. A., Pal, B., Vaillant, F., Gandolfo, L. C., Liu, Z.-Y., Blériot, C., Ginhoux, F., Smyth, G., Lindeman, G., Mueller, S. N., et al. (2020) · Nature Cell Biology · doi:10.1038/s41556-020-0505-0 · Cited by 149 · see citing works
Self-citationWang, P. L., Yim, A. K., Kim, K.-W., Avey, D. R., Czepielewski, R. S., Colonna, M., Milbrandt, J., Randolph, G. J., & The Immunological Genome Project (2020) · Nature Communications · doi:10.1038/s41467-020-16355-w · Cited by 168 · see citing works
Wang, Y., Sano, S., Yura, Y., Ke, Z., Sano, M., Oshima, K., Ogawa, H., Horitani, K., Min, K.-D., Miura-Yura, E., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.135204 · Cited by 167 · see citing works
Airway remodelling in asthma and the epithelium: on the edge of a new era
Varricchi, G., Brightling, C. E., Grainge, C., Lambrecht, B. N., & Chanez, P. (2024) · European Respiratory Journal · doi:10.1183/13993003.01619-2023 · Cited by 166 · see citing works
Dynamics of monocyte-derived macrophage diversity in experimental myocardial infarction
Rizzo, G., Gropper, J., Piollet, M., Vafadarnejad, E., Rizakou, A., Bandi, S. R., Arampatzi, P., Krammer, T., DiFabion, N., Dietrich, O., et al. (2023) · Cardiovascular Research · doi:10.1093/cvr/cvac113 · Cited by 165 · see citing works
Inducible 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
Immune responses during COVID-19 infection
Melenotte, C., Silvin, A., Goubet, A., Lahmar, I., Dubuisson, A., Zumla, A. I., Raoult, D., Merad-Boudia, M., Gachot, B., Henon, C., et al. (2020) · OncoImmunology · doi:10.1080/2162402x.2020.1807836 · Cited by 162 · see citing works
Self-citationFrancisco, J. J., & Re, D. P. D. (2023) · Antioxidants · doi:10.3390/antiox12111944 · Cited by 160 · see citing works
A census of the lung: CellCards from LungMAP
Sun, X., Perl, A. T., Li, R., Bell, S. M., Sajti, E., Kalinichenko, V. V., Kalin, T. V., Misra, R. S., Deshmukh, H. S., Clair, G., et al. (2021) · Developmental Cell · doi:10.1016/j.devcel.2021.11.007 · Cited by 157 · see citing works
pH sensing at the intersection of tissue homeostasis and inflammation
Hajjar, S., & Zhou, X. (2023) · Trends in Immunology · doi:10.1016/j.it.2023.08.008 · Cited by 157 · see citing works
Immune Cell Subtypes and Their Function in the Testis
Bhushan, S., Theas, M. S., Guazzone, V. A., Jacobo, P. V., Wang, M., Fijak, M., Meinhardt, A., & Lustig, L. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.583304 · Cited by 153 · see citing works
Wang, Z., Wu, Z., Wang, H., Feng, R., Wang, G., Li, M., Wang, S.-Y., Chen, X., Su, Y., Wang, J., et al. (2023) · Cell · doi:10.1016/j.cell.2023.08.019 · Cited by 152 · see citing works
Self-citationImmune and non-immune functions of adipose tissue leukocytes
Trim, W. V., & Lynch, L. (2021) · Nature reviews. Immunology · doi:10.1038/s41577-021-00635-7 · Cited by 147 · see citing works
Tissue‐resident innate immunity in the lung
Ardain, A., Marakalala, M. J., & Leslie, A. J. (2019) · Immunology · doi:10.1111/imm.13143 · Cited by 142 · see citing works
Resident cardiac macrophages: Heterogeneity and function in health and disease
Zaman, R., & Epelman, S. (2022) · Immunity · doi:10.1016/j.immuni.2022.08.009 · Cited by 141 · see citing works
Geldhof, V., de Rooij, L. P. M. H., Sokol, L., Amersfoort, J., Schepper, M. D., Rohlenová, K., Hoste, G., Vanderstichele, A., Delsupehe, A.-M., Isnaldi, E., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-33052-y · Cited by 141 · see citing works
Louwe, P. A., Gomez, L. B., Webster, H. C., Perona‐Wright, G., Bain, C. C., Forbes, S. J., & Jenkins, S. J. (2021) · Nature Communications · doi:10.1038/s41467-021-21778-0 · Cited by 140 · see citing works
- Authors
- Chakarov, S., Lim, H. Y., Tan, L., Lim, S. Y., See, P., Lum, J., Zhang, X.-M., Foo, S., Nakamizo, S., Duan, K., Kong, W. T., Gentek, R., Balachander, A., Carbajo, D., Bleriot, C., Malleret, B., Tam, J. K. C., Baig, S., Shabeer, M., Toh, S.-A. E. S., Schlitzer, A., Larbi, A., Marichal, T., Malissen, B., Chen, J., Poidinger, M., Kabashima, K., Bajenoff, M., Ng, L. G., Angeli, V., & Ginhoux, F.
- Affiliations
- Agency for Science, Technology and Research (SG)
- National University of Singapore (SG)
- Singapore Immunology Network (SIgN), A*STAR, 8A Biomedical Grove, Immunos Building, Level 3, Singapore 138648, Singapore.
- Centre National de la Recherche Scientifique (FR)
- University of Bonn (DE)
- University of Liège (BE)
- Centre d’Immunologie de Marseille-Luminy, Aix Marseille Université, INSERM, CNRS, 13288 Marseille, France.
- Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore.
- Corresponding author
- Ginhoux, Florent
- ORCID
- Chakarov, Svetoslav
- Lim, Hwee Ying
- Tan, Leonard
- Lim, Sheau Yng
- See, Peter
- Lum, Josephine
- Foo, Shihui
- Nakamizo, Satoshi
- Duan, Kaibo
- Kong, Wan Ting
- Gentek, Rebecca
- Balachander, Akhila
- Carbajo, Daniel
- Malleret, Benoit
- Tam, John Kit Chung
- Baig, Sonia
- Shabeer, Muhammad
- Toh, Sue-Anne Ee Shiow
- Schlitzer, Andreas
- Larbi, Anis
- Marichal, Thomas
- Malissen, Bernard
- Chen, Jinmiao
- Poidinger, Michael
- Kabashima, Kenji
- Ng, Lai Guan
- Angeli, Veronique
- Ginhoux, Florent
- Venue
- Science
- Published
- 2019-03-15
- Volume
- 363
- Issue
- 6432
- Pages
- eaau0964
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2921168633
- Cited by
- 1,114
- References
- 68
- Citations by year
- 2026: 140 · 2025: 173 · 2024: 176 · 2023: 175 · 2022: 157 · 2021: 123 · 2020: 115 · 2019: 54
- FWCI
- 44.55
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- National University of Singapore (submittedVersion)
- HAL AMU (submittedVersion)
- ORBi (University of Liège) (submittedVersion)
- Funders
- AXA Research Fund
- Singapore Immunology Institute
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Life Sciences › Neuroscience › Neurology › Neuroinflammation and Neurodegeneration Mechanisms
- Keywords
- interstitial macrophages, alveolar macrophages, macrophage heterogeneity, macrophage ontogeny, lung macrophages, single-cell RNA sequencing, fate mapping
- MeSH terms
- CX3C Chemokine Receptor 1, Animals, Histocompatibility Antigens Class II, Antigens, Ly, Disease Models, Animal, Fibrosis, Glycoproteins, Lung, Macrophages, Mice, Inbred C57BL, Monocytes, Myocardium, Sequence Analysis, RNA, Cell Lineage, Dermis, Membrane Transport Proteins, Organic Anion Transporters, Mice, Single-Cell Analysis, Transcriptome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review