Macrophage function in tissue repair and remodeling requires IL-4 or IL-13 with apoptotic cells
Open accessAbstract
Tissue repair is a subset of a broad repertoire of interleukin-4 (IL-4)- and IL-13-dependent host responses during helminth infection. Here we show that IL-4 or IL-13 alone was not sufficient, but IL-4 or IL-13 together with apoptotic cells induced the tissue repair program in macrophages. Genetic ablation of sensors of apoptotic cells impaired the proliferation of tissue-resident macrophages and the induction of anti-inflammatory and tissue repair genes in the lungs after helminth infection or in the gut after induction of colitis. By contrast, the recognition of apoptotic cells was dispensable for cytokine-dependent induction of pattern recognition receptor, cell adhesion, or chemotaxis genes in macrophages. Detection of apoptotic cells can therefore spatially compartmentalize or prevent premature or ectopic activity of pleiotropic, soluble cytokines such as IL-4 or IL-13.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
Anti-inflammatory processes mediated by IL-4 provide benefits in models representing early stages of neurodegenerative conditions such as AD and amyotrophic lateral sclerosis.
“Anti-inflammatory processes are associated with tissue repair, such as those mediated by IL-4, working through microglia and macrophages, and have been shown to provide benefits in models representing the early stages of neurodegenerative conditions, such as AD and amyotrophic lateral sclerosis, and other disorders related to cell death (45,72,73).”
From <i>Trem2</i> promotes anti-inflammatory responses in microglia and is suppressed under pro-inflammatory conditions (2020) · cites this paper as [72]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Love, M. I., Huber, W., & Anders, S. (2014) · Genome Biology · doi:10.1186/s13059-014-0550-8 · Cited by 95,106 · see citing works
Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources
Huang, D. W., Sherman, B. T., & Lempicki, R. A. (2009) · Nature Protocols · doi:10.1038/nprot.2008.211 · Cited by 35,890 · see citing works
Kim, D., Pertea, G., Trapnell, C., Pimentel, H., Kelley, R., & Salzberg, S. L. (2013) · Genome Biology · doi:10.1186/gb-2013-14-4-r36 · Cited by 12,668 · see citing works
Macrophage activation and polarization: nomenclature and experimental guidelines
Murray, P. J., Allen, J. E., Biswas, S. K., Fisher, E. A., Gilroy, D. W., Goerdt, S., Gordon, S., Hamilton, J. A., Ivashkiv, L. B., Lawrence, T., et al. (2014) · Immunity · doi:10.1016/j.immuni.2014.06.008 · Cited by 6,337 · see citing works
Alternative activation of macrophages: mechanism and functions
Gordon, S., & Martinez, F. O. (2010) · Immunity · doi:10.1016/j.immuni.2010.05.007 · Cited by 4,197 · see citing works
Metsalu, T., & Vilo, J. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv468 · Cited by 3,729 · see citing works
Fadok, V. A., Voelker, D. R., Campbell, P. A., Cohen, J., Bratton, D. L., & Henson, P. M. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.148.7.2207 · Cited by 3,321 · see citing works
Macrophage plasticity and polarization in tissue repair and remodelling
Mantovani, A., Biswas, S. K., Galdiero, M. R., Sica, A., & Locati, M. (2013) · The Journal of Pathology · doi:10.1002/path.4133 · Cited by 2,384 · 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 · see citing works
Jenkins, S., Ruckerl, D., Cook, P., Jones, L., Finkelman, F., van Rooijen, N., MacDonald, A., & Allen, J. (2011) · Science · doi:10.1126/science.1204351 · Cited by 1,427 · see citing works
Eosinophils Sustain Adipose Alternatively Activated Macrophages Associated with Glucose Homeostasis
Wu, D., Molofsky, A. B., Liang, H.-E., Ricardo-González, R. R., Jouihan, H. A., Bando, J. K., Chawla, A., & Locksley, R. M. (2011) · Science · doi:10.1126/science.1201475 · Cited by 1,380 · see citing works
Apoptotic cell clearance: basic biology and therapeutic potential
Poon, I. K. H., Lucas, C. D., Rossi, A. G., & Ravichandran, K. S. (2014) · Nature Reviews Immunology · doi:10.1038/nri3607 · Cited by 1,223 · see citing works
Dyken, S. V. V., & Locksley, R. (2013) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032712-095906 · Cited by 700 · see citing works
Kong, Y. (2011) · Genomics · doi:10.1016/j.ygeno.2011.05.009 · Cited by 580 · see citing works
Urban, J. F., Noben-Trauth, N., Donaldson, D. D., Madden, K. B., Morris, S. C., Collins, M. A., & Finkelman, F. D. (1998) · Immunity · doi:10.1016/s1074-7613(00)80477-x · Cited by 579 · see citing works
TAM Receptor Signaling in Immune Homeostasis
Rothlin, C. V., Silva, E. A. C., Bosurgi, L., & Ghosh, S. (2015) · Annual Review of Immunology · doi:10.1146/annurev-immunol-032414-112103 · Cited by 516 · see citing works
Tyro-3 family receptors are essential regulators of mammalian spermatogenesis
Lu, Q., Gore, M., Zhang, Q., Camenisch, T., Boast, S., Casagranda, F., Lai, C., Skinner, M. K., Klein, R., Matsushima, G. K., et al. (1999) · Nature · doi:10.1038/19554 · Cited by 514 · see citing works
Chen, F., Liu, Z., Wu, W., Rozo, C. T., Bowdridge, S. A. A., Millman, A., van Rooijen, N., Urban, J. F., Wynn, T. A., & Gause, W. C. (2012) · Nature Medicine · doi:10.1038/nm.2628 · Cited by 451 · see citing works
Differential expression of FIZZ1 and Ym1 in alternatively versus classically activated macrophages
Raes, G., BAETSELIER, P. D., Noël, W., Beschin, A., Brombacher, F., & Gh., G. H. (2002) · Journal of Leukocyte Biology · doi:10.1189/jlb.71.4.597 · Cited by 443 · see citing works
Deficiency or inhibition of Gas6 causes platelet dysfunction and protects mice against thrombosis
Angelillo-Scherrer, A., de Frutos, P. G., Aparicio, C., Melis, E., Savi, P., Lupu, F., Arnout, J., Dewerchin, M., Hoylaerts, M. F., Herbert, J.-M., et al. (2001) · Nature Medicine · doi:10.1038/84667 · Cited by 441 · see citing works
Diversification of TAM receptor tyrosine kinase function
Zagórska, A., Través, P. G., Lew, E. D., Dransfield, I., & Lemke, G. (2014) · Nature Immunology · doi:10.1038/ni.2986 · Cited by 430 · see citing works
Impaired Development of Th2 Cells in IL-13-Deficient Mice
McKenzie, G. J., Emson, C. L., Bell, S. E., Anderson, S. M., Fallon, P. G., Zurawski, G., Murray, R., Grencis, R. K., & McKenzie, A. N. J. (1998) · Immunity · doi:10.1016/s1074-7613(00)80625-1 · Cited by 381 · see citing works
Gundra, U. M., Girgis, N. M., Ruckerl, D., Jenkins, S., Ward, L. N., Kurtz, Z. D., Wiens, K. E., Tang, M. S., Basu-Roy, U., Mansukhani, A., et al. (2014) · Blood · doi:10.1182/blood-2013-08-520619 · Cited by 371 · see citing works
Voehringer, D., Reese, T. A., Huang, X., Shinkai, K., & Locksley, R. M. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20052448 · Cited by 349 · see citing works
Savill, J., Henson, P. M., & Haslett, C. (1989) · Journal of Clinical Investigation · doi:10.1172/jci114328 · Cited by 291 · see citing works
TAM receptor function in the retinal pigment epithelium
Prasad, D., Rothlin, C. V., Burrola, P., Burstyn-Cohen, T., Lu, Q., Garcia de Frutos, P., & Lemke, G. (2006) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2006.06.011 · Cited by 270 · see citing works
Macrophages and fibroblasts express embryonic fibronectins during cutaneous wound healing.
Brown, L. F., Dubin, D. B., Lavigne, L. M., Logan, B., Dvorak, H. F., & Water, L. V. D. (1993) · PubMed Central · Cited by 192 · see citing works
Paul, W. E. (2015) · Cytokine · doi:10.1016/j.cyto.2015.01.038 · Cited by 178 · see citing works
Differential Macrophage Activation Alters the Expression Profile of NTPDase and Ecto-5′-Nucleotidase
Zanin, R. F., Braganhol, E., Bergamin, L. S., Campesato, L. F., Zanotto‐Filho, A., Moreira, J. C. F., Morrone, F. B., Sévigny, J., Schetinger, M. R. C., Wyse, Â. T. D. S., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0031205 · Cited by 157 · see citing works
Paradoxical role of the proto-oncogene Axl and Mer receptor tyrosine kinases in colon cancer
Bosurgi, L., Bernink, J. H., Cuevas, V. D., Gagliani, N., Joannas, L. D., Schmid, E. T., Booth, C. J., Ghosh, S., & Rothlin, C. V. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302507110 · Cited by 151 · see citing works
The TAM family receptor tyrosine kinase TYRO3 is a negative regulator of type 2 immunity
Chan, P. Y., Silva, E. A. C., de Kouchkovsky, D. A., Joannas, L. D., Hao, L., Hu, D., Huntsman, S., Eng, C. S., Licona-Limón, P., Weinstein, J. S., et al. (2016) · Science · doi:10.1126/science.aaf1358 · Cited by 92 · see citing works
AXL receptor tyrosine kinase is required for T cell priming and antiviral immunity
Schmid, E. T., Pang, I. K., Silva, E. A. C., Bosurgi, L., Miner, J. J., Diamond, M., Iwasaki, A., & Rothlin, C. V. (2016) · eLife · doi:10.7554/elife.12414 · Cited by 81 · see citing works
Galizzi, J., Zuber, C. E., Cabrillat, H., Djossou, O., & Banchereau, J. (1989) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)83528-1 · Cited by 61 · see citing works
Flagged first, then by citations
Research works printed but not linked: 1
- [7]Brown LF Am J Pathol 142 793 801 1993 8456940 PMC1886786
Cited by
Sorted by citations
Diversity, Mechanisms, and Significance of Macrophage Plasticity
Locati, M., Curtale, G., & Mantovani, A. (2020) · Annual Review of Pathology: Mechanisms of Disease · doi:10.1146/annurev-pathmechdis-012418-012718 · Cited by 2,199 · see citing works
Type 2 immunity in tissue repair and fibrosis
Gieseck, R. L., Wilson, M. S., & Wynn, T. A. (2018) · Nature Reviews Immunology · doi:10.1038/nri.2017.90 · Cited by 1,055 · see citing works
The clearance of dead cells by efferocytosis
Boada-Romero, E., Martinez, J., Heckmann, B. L., & Green, D. R. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-0232-1 · Cited by 893 · see citing works
Wen, Y., Lambrecht, J., Ju, C., & Tacke, F. (2021) · Cellular & Molecular Immunology · doi:10.1038/s41423-020-00558-8 · Cited by 695 · 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
The Coming Decade of Cell Death Research: Five Riddles
Green, D. R. (2019) · Cell · doi:10.1016/j.cell.2019.04.024 · Cited by 561 · see citing works
Macrophages in wound healing: activation and plasticity
Kim, S. Y., & Nair, M. G. (2019) · Immunology and Cell Biology · doi:10.1111/imcb.12236 · Cited by 536 · see citing works
The Role of IL-6 in Skin Fibrosis and Cutaneous Wound Healing
Johnson, B. Z., Stevenson, A. W., Prêle, C. M., Fear, M. W., & Wood, F. M. (2020) · Biomedicines · doi:10.3390/biomedicines8050101 · Cited by 532 · see citing works
Mack, M. (2017) · Matrix Biology · doi:10.1016/j.matbio.2017.11.010 · Cited by 516 · see citing works
Zhang, S., Weinberg, S., DeBerge, M., Gainullina, A., Schipma, M., Kinchen, J. M., Ben-Sahra, I., Gius, D. R., Yvan-Charvet, L., Chandel, N. S., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2018.12.004 · Cited by 485 · see citing works
The initiation of oxidative stress and therapeutic strategies in wound healing.
Wang, G., Yang, F., Zhou, W., Xiao, N.-Y., Luo, M., & Tang, Z. (2022) · Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · doi:10.1016/j.biopha.2022.114004 · Cited by 388 · see citing works
Living on the Edge: Efferocytosis at the Interface of Homeostasis and Pathology
Morioka, S., Maueröder, C., & Ravichandran, K. S. (2019) · Immunity · doi:10.1016/j.immuni.2019.04.018 · Cited by 391 · see citing works
Type 2 immunity in allergic diseases
Öğülür, İ., Mitamura, Y., Yazıcı, D., Pat, Y., Ardıçlı, S., Li, M., D’Avino, P., Beha, C., Babayev, H., Zhao, B., et al. (2025) · Cellular and Molecular Immunology · doi:10.1038/s41423-025-01261-2 · Cited by 413 · see citing works
Liver ischaemia–reperfusion injury: a new understanding of the role of innate immunity
Hirao, H., Nakamura, K., & Kupiec‐Weglinski, J. W. (2021) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-021-00549-8 · Cited by 371 · 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
Efferocytosis induces macrophage proliferation to help resolve tissue injury
Gerlach, B. D., Ampomah, P. B., Yurdagul, A., Liu, C., Lauring, M. C., Wang, X., Kasikara, C., Kong, N., Shi, J., Tao, W., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.10.015 · Cited by 360 · see citing works
Immunomodulatory Biomaterials for Tissue Repair
Whitaker, R. C., Hernaez‐Estrada, B., Hernández, R. M., Santos‐Vizcaíno, E., & Spiller, K. L. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00895 · Cited by 345 · see citing works
Type 2 immunity: Expanding our view
Lloyd, C. M., & Snelgrove, R. J. (2018) · Science Immunology · doi:10.1126/sciimmunol.aat1604 · Cited by 333 · see citing works
Metabolic orchestration of the wound healing response
Eming, S. A., Murray, P. J., & Pearce, E. J. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.07.017 · Cited by 319 · see citing works
Tumor-associated macrophages in cancer: recent advancements in cancer nanoimmunotherapies
Kumari, N., & Choi, S. H. (2022) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-022-02272-x · Cited by 324 · 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
Willenborg, S., Sanin, D. E., Jais, A., Ding, X., Ulas, T., Nüchel, J., Popović, M., MacVicar, T., Langer, T., Schultze, J. L., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.10.004 · Cited by 310 · see citing works
Integrative Physiology of Pneumonia
Quinton, L. J., Walkey, A. J., & Mizgerd, J. P. (2018) · Physiological Reviews · doi:10.1152/physrev.00032.2017 · Cited by 308 · see citing works
Polarized Macrophages in Periodontitis: Characteristics, Function, and Molecular Signaling
Sun, X., Gao, J., Meng, X. L., Lu, X., Zhang, L., & Chen, R. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.763334 · Cited by 294 · see citing works
Mei, J., Xu, D., Wang, L., Kong, L., Liu, Q., Li, Q., Zhang, X., Su, Z., Hu, X., Zhu, W., et al. (2023) · Advanced Materials · doi:10.1002/adma.202303432 · Cited by 280 · 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
Innate immune cell-epithelial crosstalk during wound repair.
Brazil, J., Quirós, M., Nusrat, A., & Parkos, C. (2019) · Journal of Clinical Investigation · doi:10.1172/jci124618 · Cited by 225 · see citing works
Zebrafish Regulatory T Cells Mediate Organ-Specific Regenerative Programs
Hui, S. P., Sheng, D. Z., Sugimoto, K., González-Rajal, Á., Nakagawa, S., Hesselson, D., & Kikuchi, K. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.11.010 · Cited by 269 · see citing works
Acute Inflammation in Tissue Healing
Soliman, A. M., & Barreda, D. R. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms24010641 · Cited by 283 · see citing works
Harnessing innate immune pathways for therapeutic advancement in cancer
Hu, A.-K., Sun, L., Lin, H., Liao, Y., Yang, H., & Mao, Y. Q. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01765-9 · Cited by 265 · see citing works
Das, U. N. (2018) · Journal of Advanced Research · doi:10.1016/j.jare.2018.01.001 · Cited by 256 · see citing works
Macrophages transfer mitochondria to sensory neurons to resolve inflammatory pain
van der Vlist, M., Raoof, R., Willemen, H. L. D. M., Prado, J., Versteeg, S., Gil, C. M., Vos, M. W., Lokhorst, R. E., Pasterkamp, R. J., Kojima, T., et al. (2021) · Neuron · doi:10.1016/j.neuron.2021.11.020 · Cited by 257 · see citing works
DeBerge, M., Yeap, X. Y., Dehn, S., Zhang, S., Grigoryeva, L. S., Misener, S., Procissi, D., Zhou, X., Lee, D. C., Müller, W. A., et al. (2017) · Circulation Research · doi:10.1161/circresaha.117.311327 · Cited by 241 · see citing works
Mahmoud, N. N., Hamad, K. M., Shibitini, A. A., Juma, S., Sharifi, S., Gould, L., & Mahmoudi, M. (2024) · ACS Pharmacology & Translational Science · doi:10.1021/acsptsci.3c00336 · Cited by 210 · see citing works
The Neutrophil’s Choice: Phagocytose vs Make Neutrophil Extracellular Traps
Manfredi, A. A., Ramirez, G. A., Rovere, P. Q., & Maugeri, N. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00288 · Cited by 220 · see citing works
Svedberg, F. R., Brown, S. L., Krauss, M. Z., Campbell, L., Sharpe, C., Clausen, M., Howell, G. J., Clark, H. W., Madsen, J., Evans, C. M., et al. (2019) · Nature Immunology · doi:10.1038/s41590-019-0352-y · Cited by 219 · see citing works
Tumor-associated myeloid cells: diversity and therapeutic targeting
Mantovani, A., Marchesi, F., Jaillon, S., Garlanda, C., & Allavena, P. (2021) · Cellular and Molecular Immunology · doi:10.1038/s41423-020-00613-4 · Cited by 218 · see citing works
Liu, W., Taso, O., Wang, R., Bayram, S., Graham, A. C., Garcia-Reitboeck, P., Mallach, A., Andrews, W. D., Piers, T. M., Botia, J. A., et al. (2020) · Human Molecular Genetics · doi:10.1093/hmg/ddaa209 · Cited by 214 · see citing works
“Antiinflammatory processes are associated with tissue repair, such as those mediated by IL-4, working through microglia and macrophages, and have been shown to provide benefits in models representing the early stages of neurodegenerative conditions, such as AD and amyotrophic lateral sclerosis, and other disorders rel…”
BackgroundRecent Advances in Type-2-Cell-Mediated Immunity: Insights from Helminth Infection
Harris, N. L., & Loke, P. (2017) · Immunity · doi:10.1016/j.immuni.2017.11.015 · Cited by 211 · see citing works
Malainou, C., Abdin, S. M., Lachmann, N., Matt, U., & Herold, S. (2023) · Journal of Clinical Investigation · doi:10.1172/jci170501 · Cited by 210 · see citing works
Deep insight into cytokine storm: from pathogenesis to treatment
Nie, J., Zhou, L., Tian, W., Liu, X., Yang, L., Yang, X., Zhang, Y., Wei, S., Wang, D. W., & Wei, J. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02178-y · Cited by 224 · see citing works
Macrophage Clearance of Apoptotic Cells: A Critical Assessment
Gordon, S., & Plüddemann, A. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00127 · Cited by 201 · see citing works
Cytotoxic CD4+ T lymphocytes may induce endothelial cell apoptosis in systemic sclerosis
Maehara, T., Kaneko, N., Perugino, C. A., Mattoo, H., Kers, J., Allard‐Chamard, H., Mahajan, V. S., Liu, H., Murphy, S. J. H., Ghebremichael, M. S., et al. (2020) · Journal of Clinical Investigation · doi:10.1172/jci131700 · Cited by 193 · see citing works
Molecular Mechanisms Modulating the Phenotype of Macrophages and Microglia
Amici, S. A., Dong, J., & Guerau‐de‐Arellano, M. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01520 · Cited by 192 · see citing works
Flipping the dogma – phosphatidylserine in non-apoptotic cell death
Shlomovitz, I., Speir, M., & Gerlic, M. (2019) · Cell Communication and Signaling · doi:10.1186/s12964-019-0437-0 · Cited by 184 · see citing works
M2 macrophages in kidney disease: biology, therapies, and perspectives
Chen, T., Cao, Q., Wang, Y., & Harris, D. C. H. (2019) · Kidney International · doi:10.1016/j.kint.2018.10.041 · Cited by 189 · see citing works
Zheng, Z., Chen, Y., Wu, D., Wang, J., Lv, M.-M., Wang, X., Sun, J., & Zhang, Z. (2018) · Theranostics · doi:10.7150/thno.28315 · Cited by 188 · see citing works
Adaptation and memory in immune responses
Natoli, G., & Ostuni, R. (2019) · Nature Immunology · doi:10.1038/s41590-019-0399-9 · Cited by 186 · see citing works
MYC Instructs and Maintains Pancreatic Adenocarcinoma Phenotype
Sodir, N. M., Kortlever, R. M., Barthet, V. J. A., Campos, T., Pellegrinet, L., Kupczak, S., Anastasiou, P., Swigart, L. B., Soucek, L., Arends, M. J., et al. (2020) · Cancer Discovery · doi:10.1158/2159-8290.cd-19-0435 · Cited by 183 · see citing works
The role of efferocytosis‐fueled macrophage metabolism in the resolution of inflammation
Schilperoort, M., Ngai, D., Sukka, S. R., Avrampou, K., Shi, H., & Tabas, I. A. (2023) · Immunological Reviews · doi:10.1111/imr.13214 · Cited by 181 · see citing works
Metabolic adaptations of tissue-resident immune cells
Caputa, G., Castoldi, Â., & Pearce, E. J. (2019) · Nature Immunology · doi:10.1038/s41590-019-0407-0 · Cited by 176 · see citing works
Carestia, A., Mena, H. A., Olexen, C. M., Wilczyński, J., Negrotto, S., Errasti, A. E., Gomez, R. M., Jenne, C. N., Silva, E. A. C., & Schattner, M. A. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.06.062 · Cited by 175 · see citing works
Regulatory T cells in skin injury: At the crossroads of tolerance and tissue repair
Boothby, I. C., Cohen, J. N., & Rosenblum, M. D. (2020) · Science Immunology · doi:10.1126/sciimmunol.aaz9631 · Cited by 174 · see citing works
Regulation and Functions of 15-Lipoxygenases in Human Macrophages
Snodgrass, R. G., & Brüne, B. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00719 · Cited by 162 · see citing works
Function of Macrophages in Disease: Current Understanding on Molecular Mechanisms
Zhang, C., Yang, M. J., & Ericsson, A. C. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.620510 · Cited by 162 · see citing works
Satyanarayanan, S. K., Kebir, D. E., Soboh, S., Butenko, S., Sekheri, M., Saadi, J., Peled, N., Assi, S., Othman, A., Schif‐Zuck, S., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10903-9 · Cited by 160 · see citing works
Airway macrophages as the guardians of tissue repair in the lung
Puttur, F. K., Gregory, L. G., & Lloyd, C. M. (2019) · Immunology and Cell Biology · doi:10.1111/imcb.12235 · Cited by 157 · see citing works
Disease Tolerance as an Inherent Component of Immunity
Martins, R., Carlos, A. R., Braza, F., Thompson, J. A., Bastos-Amador, P., Ramos, S., & Soares, M. P. (2019) · Annual Review of Immunology · doi:10.1146/annurev-immunol-042718-041739 · Cited by 149 · see citing works
A common framework of monocyte-derived macrophage activation
Sanin, D. E., Ge, Y., Marinković, E., Kabat, A. M., Castoldi, Â., Caputa, G., Grzes, K. M., Curtis, J. D., Thompson, E. A., Willenborg, S., et al. (2022) · Science Immunology · doi:10.1126/sciimmunol.abl7482 · Cited by 153 · see citing works
Role of Macrophages in Wound HealingPreprint
Willenborg, S., Injarabian, L., & Eming, S. A. (2022) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a041216 · Cited by 147 · see citing works
Sulfated Chitosan Rescues Dysfunctional Macrophages and Accelerates Wound Healing in Diabetic Mice.
Shen, T., Dai, K., Yu, Y.-M., Wang, J., & Liu, C.-S. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.09.035 · Cited by 130 · see citing works
Patil, P., Russo, K. A., McCune, J. T., Pollins, A. C., Cottam, M. A., Dollinger, B. R., DeJulius, C. R., Gupta, M. K., d’Arcy, R., Colazo, J. M., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abm6586 · Cited by 141 · see citing works
IL-33 drives group 2 innate lymphoid cell-mediated protection during Clostridium difficile infection
Frisbee, A. L., Saleh, M. M., Young, M. K., Leslie, J. L., Simpson, M. D., Abhyankar, M. M., Cowardin, C. A., Ma, J. Z., Pramoonjago, P., Turner, S., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-10733-9 · Cited by 137 · see citing works
Th1, Th2, and Th17 cytokines in systemic lupus erythematosus
Yusoff, F. M., Wong, K. K., & Redzwan, N. M. (2019) · Autoimmunity · doi:10.1080/08916934.2019.1693545 · Cited by 134 · see citing works
Synovial tissue macrophages: friend or foe?
Kurowska‐Stolarska, M., & Alivernini, S. (2017) · RMD Open · doi:10.1136/rmdopen-2017-000527 · Cited by 133 · see citing works
Ortega, R. H., Cerezo, A. B., de Pablos, R. M., Krisa, S., Richard, T., García-Parrilla, M. C., & Troncoso, A. M. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00373 · Cited by 130 · see citing works
The Antisocial Network: Cross Talk Between Cell Death Programs in Host Defense
Snyder, A. G., & Oberst, A. (2021) · Annual Review of Immunology · doi:10.1146/annurev-immunol-112019-072301 · Cited by 129 · see citing works
Cabeza-Cabrerizo, M., van Blijswijk, J., Wienert, S., Heim, D., Jenkins, R. P., Chakravarty, P., Rogers, N. C., Frederico, B., Acton, S. E., Beerling, E., et al. (2019) · Science Immunology · doi:10.1126/sciimmunol.aaw1941 · Cited by 126 · see citing works
Zou, M., Sun, J., & Xiang, Z. (2021) · Advanced Healthcare Materials · doi:10.1002/adhm.202001502 · Cited by 124 · see citing works
Tuning the Tumor Myeloid Microenvironment to Fight Cancer
Jahchan, N. S., Mujal, A. M., Pollack, J. L., Binnewies, M., Sriram, V., Reyno, L. M., & Krummel, M. F. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01611 · Cited by 120 · see citing works
Lee, S. H., Charmoy, M., Romano, A., Paun, A., Chaves, M. M., Cope, F. O., Ralph, D. A., & Sacks, D. L. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20171389 · Cited by 120 · see citing works
Neutrophil–macrophage cooperation and its impact on tissue repair
Bouchery, T., & Harris, N. L. (2019) · Immunology and Cell Biology · doi:10.1111/imcb.12241 · Cited by 119 · see citing works
Heterogeneity in the initiation, development and function of type 2 immunity
Gause, W. C., Rothlin, C. V., & Loke, P. (2020) · Nature reviews. Immunology · doi:10.1038/s41577-020-0301-x · Cited by 117 · see citing works
Mechanisms of urodele limb regeneration
Stocum, D. L. (2017) · Regeneration · doi:10.1002/reg2.92 · Cited by 115 · see citing works
Neuroimmunophysiology of the gut: advances and emerging concepts focusing on the epithelium
Sharkey, K. A., Beck, P. L., & McKay, D. M. (2018) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-018-0051-4 · Cited by 116 · see citing works
Sommer, K., Wiendl, M., Müller, T., Heidbreder, K., Voskens, C., Neurath, M., & Zundler, S. (2021) · Frontiers in Medicine · doi:10.3389/fmed.2021.643973 · Cited by 97 · see citing works
Mechanosensing regulates tissue repair program in macrophages
Meizlish, M. L., Kimura, Y., Pope, S. D., Matta, R., Kim, C., Philip, N. H., Meyaard, L., Gonzalez, A., & Medzhitov, R. (2024) · Science Advances · doi:10.1126/sciadv.adk6906 · Cited by 114 · see citing works
The Dynamic Inflammatory Tissue Microenvironment: Signality and Disease Therapy by Biomaterials
Mata, R., Yao, Y., Cao, W., Ding, J., Zhou, T., Zhai, Z., & Gao, C.-Y. (2021) · Research · doi:10.34133/2021/4189516 · Cited by 112 · see citing works
Senescent cells suppress macrophage-mediated corpse removal via upregulation of the CD47-QPCT/L axis
Schloesser, D., Lindenthal, L., Sauer, J., Chung, K., Chavakis, T., Griesser, E., Baskaran, P., Maier-Habelsberger, U., Fundel‐Clemens, K., Schlotthauer, I., et al. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202207097 · Cited by 113 · see citing works
Zhang, H., Xu, A.-D., Sun, X., Yang, Y., Zhang, L., Bai, H., Ben, J., Zhu, X., Li, X., Yang, Q., et al. (2020) · Circulation Research · doi:10.1161/circresaha.119.316428 · Cited by 108 · see citing works
Chakraborty, S., Singh, A., Wang, L. X., Wang, X., Sanborn, M. A., Ye, Z., Maienschein‐Cline, M., Mukhopadhyay, A., Ganesh, B. B., Malik, A. B., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20221388 · Cited by 111 · see citing works
Campana, L., Starkey Lewis, P. J., Pellicoro, A., Aucott, R. L., Man, J., O’Duibhir, E., Mok, S. E., Ferreira-Gonzalez, S., Livingstone, E., Greenhalgh, S. N., et al. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701247 · Cited by 107 · see citing works
Chen, J., Zhou, R.-P., Liang, Y.-M., Fu, X.-J., Wang, D.-R., & Wang, C. (2019) · The FASEB Journal · doi:10.1096/fj.201901610 · Cited by 97 · see citing works
The expanding world of tissue‐resident macrophages
Jenkins, S. J., & Allen, J. E. (2021) · European Journal of Immunology · doi:10.1002/eji.202048881 · Cited by 105 · see citing works
Interpreting an apoptotic corpse as anti-inflammatory involves a chloride sensing pathway
Perry, J. S. A., Morioka, S., Medina, C. B., Etchegaray, J. I., Barron, B. J., Raymond, M. H., Lucas, C. D., Önengüt-Gümüşcü, S., Delpire, E. J., & Ravichandran, K. S. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0431-1 · Cited by 106 · see citing works
Metabolic adaptation supports enhanced macrophage efferocytosis in limited-oxygen environments
Wang, Y., Trzeciak, A. J., Rojas, W. S., Saavedra, P. H. V., Chen, Y., Chirayil, R., Etchegaray, J. I., Lucas, C. D., Puleston, D. J., Keshari, K. R., et al. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.12.005 · Cited by 107 · see citing works
Pine, G. M., Batugedara, H., & Nair, M. G. (2018) · Cytokine · doi:10.1016/j.cyto.2018.05.014 · Cited by 104 · see citing works
First we eat, then we do everything else: The dynamic metabolic regulation of efferocytosis
Trzeciak, A. J., Wang, Y., & Perry, J. S. A. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.08.001 · Cited by 107 · see citing works
Ohue‐Kitano, R., Watanabe‐Yasuoka, Y., Goto, T., Kitamura, N., Park, S., Kishino, S., Kimura, I., Kasubuchi, M., Takahashi, H., Li, Y., et al. (2017) · The FASEB Journal · doi:10.1096/fj.201700273r · Cited by 103 · see citing works
Reparative and Maladaptive Inflammation in Tendon Healing
Arvind, V., & Huang, A. H. (2021) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2021.719047 · Cited by 104 · see citing works
Merlin, J., Ivanov, S., Dumont, A., Sergushichev, A., Gall, J., Stunault, M. I., Ayrault, M., Vaillant, N., Castiglione, A., Swain, A., et al. (2021) · Nature Metabolism · doi:10.1038/s42255-021-00471-y · Cited by 101 · see citing works
Iron Metabolism in the Tumor Microenvironment—Implications for Anti-Cancer Immune Response
Sacco, A., Battaglia, A. M., Botta, C., Aversa, I., Mancuso, S., Costanzo, F. S., & Biamonte, F. (2021) · Cells · doi:10.3390/cells10020303 · Cited by 100 · see citing works
Is the Macrophage Phenotype Determinant for Fibrosis Development?
Lis-López, L., Bauset, C., Seco-Cervera, M., & Cosín‐Roger, J. (2021) · Biomedicines · doi:10.3390/biomedicines9121747 · Cited by 97 · see citing works
Wu, M.-Y., Liu, L., Wang, E., Xiao, H., Cai, C.-Z., Wang, J., Su, H., Wang, Y., Tan, J., Zhang, Z., et al. (2020) · Autophagy · doi:10.1080/15548627.2020.1741332 · Cited by 95 · see citing works
The Role of Type 2 Innate Lymphoid Cells in Allergic Diseases
Zheng, H., Zhang, Y., Pan, J., Liu, N., Qin, Y., Qiu, L., Liu, M., & Wang, T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.586078 · Cited by 97 · see citing works
Tuft cells act as regenerative stem cells in the human intestine
Huang, L., Bernink, J. H., Giladi, A., Krueger, D., van Son, G. J. F., Geurts, M. H., Busslinger, G. A., Lin, L., Begthel, H., Zandvliet, M. M. J. M., et al. (2024) · Nature · doi:10.1038/s41586-024-07952-6 · Cited by 94 · see citing works
Apoptotic cell identity induces distinct functional responses to IL-4 in efferocytic macrophages
Liebold, I., Al Jawazneh, A., Casar, C., Lanzloth, C., Leyk, S., Hamley, M., Wong, M. N., Kylies, D., Gräfe, S. K., Edenhofer, I., et al. (2024) · Science · doi:10.1126/science.abo7027 · Cited by 96 · see citing works
Kumar, S., Calianese, D. C., & Birge, R. B. (2017) · Immunological Reviews · doi:10.1111/imr.12587 · Cited by 92 · see citing works
Mast Cells in Cardiac Fibrosis: New Insights Suggest Opportunities for Intervention
Legere, S. A., Haidl, I. D., Légaré, J.-F., & Marshall, J. S. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00580 · Cited by 92 · see citing works
Macrophage Phenotypes in Normal and Diabetic Wound Healing and Therapeutic Interventions
Sadoun, H. A. (2022) · Cells · doi:10.3390/cells11152430 · Cited by 95 · see citing works
- Authors
- Bosurgi, L., Cao, Y. G., Cabeza-Cabrerizo, M., Tucci, A., Hughes, L. D., Kong, Y., Weinstein, J. S., Licona-Limon, P., Schmid, E. T., Pelorosso, F., Gagliani, N., Craft, J. E., Flavell, R. A., Ghosh, S., & Rothlin, C. V.
- Affiliations
- Yale University (US)
- Department of Immunobiology, School of Medicine, Yale University, New Haven, CT 06520, USA.
- Universidad de Buenos Aires (AR)
- University Medical Center Hamburg-Eppendorf (DE)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Ghosh, Sourav
- Rothlin, Carla V.
- ORCID
- Venue
- Science
- Published
- 2017-06-09
- Volume
- 356
- Issue
- 6342
- Pages
- 1072-1076
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC5556699
- OpenAlex
- W2612072527
- Cited by
- 560
- References
- 33
- Citations by year
- 2026: 46 · 2025: 66 · 2024: 53 · 2023: 61 · 2022: 67 · 2021: 76 · 2020: 69 · 2019: 57 · 2018: 38 · 2017: 27
- FWCI
- 23.64
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Science Foundation (award305303, DGE-1122492)
- National Institutes of Health (award305299, R01 AI089824, award305300, R01CA212376, award309995, R37 AR40072, award305301, T32AI007019)
- Howard Hughes Medical Institute (award305304)
- American Italian Cancer Foundation (award305302)
- NIH (award309994, R37 AR40072)
- 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 › Parasitology › Parasites and Host Interactions
- Keywords
- macrophage function, tissue repair, tissue remodeling, IL-4, IL-13, apoptotic cells, phagocytosis, helminthiasis, colitis, tissue-resident macrophages, anti-inflammatory genes, pattern recognition receptors, cytokine signaling, lung, intestine
- MeSH terms
- Animals, Inflammation, Macrophages, Nippostrongylus, Regeneration, Thioglycolates, Interleukin-4, Strongylida Infections, Apoptosis, Interleukin-13, Mice
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