The DOI matches its Crossref record; 90 of the 90 references it cites were found in a registry or an index.
Transcriptional regulation of macrophage polarization: enabling diversity with identity
Abstract
In terms of both phenotype and function, macrophages have remarkable heterogeneity, which reflects the specialization of tissue-resident macrophages in microenvironments as different as liver, brain and bone. Also, marked changes in the activity and gene expression programmes of macrophages can occur when they come into contact with invading microorganisms or injured tissues. Therefore, the macrophage lineage includes a remarkable diversity of cells with different functions and functional states that are specified by a complex interplay between microenvironmental signals and a hardwired differentiation programme that determines macrophage identity. In this Review, we summarize the current knowledge of transcriptional and chromatin-mediated control of macrophage polarization in physiology and disease.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
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?
In the citing paper
“previous studies have reported that MAPK signaling cascades are the central pathway in the M1 polarization of macrophages.24,25”
From Sphingosine Kinase 1 Aggravates Liver Fibrosis by Mediating Macrophage Recruitment and Polarization (2024) · cites this paper as [24]
In the citing paper
“During the transition to the chronic stage of FBR macrophages switch from a pro-inflammatory activation phenotype (M1 macrophages) to an anti-inflammatory and tissue generation phenotype (M2 macrophages) (Mantovani et al., 2004; Lawrence and Natoli, 2011; Sridharan et al., 2015).”
From Foreign Body Reaction to Implanted Biomaterials and Its Impact in Nerve Neuroprosthetics (2021) · cites this paper as Lawrence and Natoli, 2011
In the citing paper
“Lawrence et al has suggested that MCSF receptor activates IRF4 transcription factor to promote M2 differentiation of macrophages [37].”
From Rac2 Controls Tumor Growth, Metastasis and M1-M2 Macrophage Differentiation In Vivo (2014) · cites this paper as [37]
In the citing paper
“While the mechanisms that underlie this observed plasticity are not well understood, recent studies have shown that a number of mutually exclusive and feed forward signaling pathways may play a role [19].”
From Macrophage polarization: an opportunity for improved outcomes in biomaterials and regenerative medicine (2012) · cites this paper as [19]
Citations
Cites
Heinz, S., Benner, C., Spann, N., Bertolino, E., Lin, Y. C., Laslo, P., Cheng, J. X., Murre, C., Singh, H., & Glass, C. K. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.05.004 · Cited by 13,382
Exploring the full spectrum of macrophage activation
Mosser, D. M., & Edwards, J. P. (2008) · Nature Reviews Immunology · doi:10.1038/nri2448 · Cited by 9,144
Darnell, J. E., Kerr, L. M., & Stark, G. R. (1994) · Science · doi:10.1126/science.8197455 · Cited by 6,080 · cited 1×
“Stimulation of the IFNγ receptor triggers JAK-mediated tyrosine phosphorylation and subsequent dimerization of STAT1, which binds as a homodimer to cis elements known as gamma-activated sequences in the promoters of the genes encoding NOS2, the MHC class II transactivator (CIITA) and IL-12, among other”
BackgroundMonocyte and macrophage heterogeneity
Gordon, S., & Taylor, P. R. (2005) · Nature Reviews Immunology · doi:10.1038/nri1733 · Cited by 5,190
Histone H3K27ac separates active from poised enhancers and predicts developmental state
Creyghton, M. P., Cheng, A. W., Welstead, G. G., Kooistra, T., Carey, B. W., Steine, E. J., Hanna, J., Lodato, M. A., Frampton, G. M., Sharp, P. A., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016071107 · Cited by 4,302
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
The peroxisome proliferator-activated receptor-γ is a negative regulator of macrophage activation
Ricote, M., Li, A. C., Willson, T. M., Kelly, C. J., & Glass, C. K. (1998) · Nature · doi:10.1038/34178 · Cited by 3,525
Blood Monocytes Consist of Two Principal Subsets with Distinct Migratory Properties
Geissmann, F., Jung, S., & Littman, D. R. (2003) · Immunity · doi:10.1016/s1074-7613(03)00174-2 · Cited by 3,504
Heintzman, N. D., Stuart, R. K., Hon, G., Fu, Y., Ching, C. W., Hawkins, R. D., Barrera, L. O., Van Calcar, S., Qu, C., Ching, K. A., et al. (2007) · Nature Genetics · doi:10.1038/ng1966 · Cited by 3,398 · cited 1×
“Genomic regions that are active as enhancers in a given cell type can be identified by their association with specific histone modifications, in particular monomethylation of lysine 4 in histone H3 (H3K4me1), although the precise functional effects of such modifications in terms of enhancer activity are still unknow”
BackgroundCpG islands and the regulation of transcription
Deaton, A. M., & Bird, A. (2011) · Genes & Development · doi:10.1101/gad.2037511 · Cited by 3,187
Flagged first, then by citations
Cited by
Sorted by citations
Items 601–700 of 1,005
Mehta, S., Cronkite, D. A., Basavappa, M. G., Saunders, T. L., Adiliaghdam, F., Amatullah, H., Morrison, S. A., Pagan, J. D., Anthony, R. M., Tonnerre, P., et al. (2017) · Science Immunology · doi:10.1126/sciimmunol.aag3160 · Cited by 69
Dugo, L., Belluomo, M. G., Fanali, C., Russo, M., Cacciola, F., Maccarrone, M., & Sardanelli, A. M. (2017) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2017/6293740 · Cited by 67
How Mitochondrial Metabolism Contributes to Macrophage Phenotype and Functions
Benmoussa, K., Garaude, J., & Acín‐Pérez, R. (2018) · Journal of Molecular Biology · doi:10.1016/j.jmb.2018.07.003 · Cited by 69
Willis, G. R., Fernandez‐Gonzalez, A., Reis, M., Mitsialis, S. A., & Kourembanas, S. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19092534 · Cited by 68
lncRNA NTT/PBOV1 Axis Promotes Monocyte Differentiation and Is Elevated in Rheumatoid Arthritis
Yang, C., Li, J., Yen, J.-C., Lai, I., Ho, Y.-C., Chen, Y., Lan, J., & Chang, J. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19092806 · Cited by 67
Sun, Y., Duan, B., Chen, H., & Xu, X. (2020) · Advanced Healthcare Materials · doi:10.1002/adhm.201901805 · Cited by 66
Shu, Y., Qin, M., Song, Y., Tang, Q., Huang, Y., Shen, P., & Lu, Y. Z. (2020) · Immunology · doi:10.1111/imm.13196 · Cited by 66
Heterogeneous Myeloid Cells in Tumors
Dou, A., & Fang, J. (2021) · Cancers · doi:10.3390/cancers13153772 · Cited by 68
Prakadan, S. M., Alvarez-Breckenridge, C. A., Markson, S. C., Kim, A. E., Klein, R. H., Nayyar, N., Navia, A. W., Kuter, B. M., Kolb, K. E., Bihun, I. V., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25860-5 · Cited by 66
Yamaguchi, T., Takizawa, F., Fischer, U., & Dijkstra, J. M. (2015) · Biology · doi:10.3390/biology4040814 · Cited by 67
MicroRNA-24 Modulates Staphylococcus aureus-Induced Macrophage Polarization by Suppressing CHI3L1
Jingjing, Z., Zhang, N., Wei, W., Qinghe, G., Wang, W., Wang, P., & Xiangpeng, W. (2017) · Inflammation · doi:10.1007/s10753-017-0543-3 · Cited by 66
Mamun, A. A., Chauhan, A., Yu, H., Xu, Y., Sharmeen, R., & Liu, F. (2017) · European Journal of Neuroscience · doi:10.1111/ejn.13778 · Cited by 66
Anisotropic Ligand Nanogeometry Modulates the Adhesion and Polarization State of Macrophages
Kang, H., Wong, S. H. D., Pan, Q., Li, G., & Bian, L. (2019) · Nano Letters · doi:10.1021/acs.nanolett.8b05150 · Cited by 67
Moradi‐Chaleshtori, M., Bandehpour, M., Soudi, S., Mohammadi‐Yeganeh, S., & Hashemi, S. M. (2020) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-020-02762-x · Cited by 66
New Insights Into Tissue Macrophages: From Their Origin to the Development of Memory
Italiani, P., & Boraschi, D. (2015) · Immune Network · doi:10.4110/in.2015.15.4.167 · Cited by 68
Peng, T., Du, S.-Y., Son, M., & Diamond, B. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2106017118 · Cited by 67
Chen, J., & Wei, H. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.718089 · Cited by 66
The role of IL-10 in Mycobacterium avium subsp. paratuberculosis infection
Hussain, T. A., Shah, S. Z. A., Zhao, D., Sreevatsan, S., & Zhou, X. (2016) · Cell Communication and Signaling · doi:10.1186/s12964-016-0152-z · Cited by 68
Neuroimmune interactions and osteoarthritis pain: focus on macrophages
Geraghty, T., Winter, D. R., Miller, R. J., Miller, R. E., & Malfait, A. (2021) · PAIN Reports · doi:10.1097/pr9.0000000000000892 · Cited by 67
Nishikawa, K., Seo, N., Torii, M., Ma, N., Muraoka, D., Tawara, I., Masuya, M., Tanaka, K., Takei, Y., Shiku, H., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108494 · Cited by 64
Zhang, Y., Liu, X., She, Z., Jiang, D.-S., Wan, N., Xia, H., Zhu, X., Xiang, W., Zhang, X., & Li, H. (2014) · Basic Research in Cardiology · doi:10.1007/s00395-014-0434-9 · Cited by 64
Innate Immune Reactions in Septic and Aseptic Osteolysis around Hip Implants
Pajarinen, J., Jämsen, E., Konttinen, Y. T., & Goodman, S. B. (2014) · Journal of Long-Term Effects of Medical Implants · doi:10.1615/jlongtermeffmedimplants.2014010564 · Cited by 67
Ozone-induced lung injury and sterile inflammation. Role of toll-like receptor 4
Connor, A. J., Laskin, J. D., & Laskin, D. L. (2012) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2012.01.004 · Cited by 64
Macrophages and pancreatic ductal adenocarcinoma
Habtezion, A., Edderkaoui, M., & Pandol, S. J. (2015) · Cancer Letters · doi:10.1016/j.canlet.2015.11.049 · Cited by 66
Chen, G., Ni, Y., Nagata, N., Zhuge, F., Xu, L., Nagashimada, M., Yamamoto, S., Ushida, Y., Fuke, N., Suganuma, H., et al. (2019) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201900602 · Cited by 64
Bi, J., Zeng, X., Zhao, L., Wei, Q., Yu, L., Wang, X., Yu, Z., Cao, Y., Shan, F., & Wei, M. (2016) · Molecular Therapy - Nucleic Acids · doi:10.1038/mtna.2016.71 · Cited by 63
RetractedTargeting STAT3 and STAT5 in Tumor-Associated Immune Cells to Improve Immunotherapy
Verdeil, G., Lawrence, T., Schmitt‐Verhulst, A., & Auphan‐Anezin, N. (2019) · Cancers · doi:10.3390/cancers11121832 · Cited by 64
Self-citationInterleukin-5-induced eosinophil population improves cardiac function after myocardial infarction
Xu, J. Y., Xiong, Y. Y., Tang, R., Jiang, W. Y., Yu, N., Gong, Z. T., Huang, P. S., Chen, G. H., Xu, J., Wu, C. X., et al. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab237 · Cited by 63
Li, J., Liu, H., Wang, X., Xia, Y. F., Huang, J., Wang, T., Lin, Z., & Xiong, N. (2022) · npj Parkinson s Disease · doi:10.1038/s41531-022-00352-5 · Cited by 63
Protective Effect of MFG-E8 after Cutaneous Ischemia–Reperfusion Injury
Uchiyama, A., Yamada, K., Perera, B., Ogino, S., Yokoyama, Y., Takeuchi, Y., Ishikawa, O., & Motegi, S. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.515 · Cited by 63
Hasegawa‐Moriyama, M., Kurimoto, T., Nakama, M., Godai, K., Kojima, M., Kuwaki, T., & Kanmura, Y. (2013) · Pain · doi:10.1016/j.pain.2013.04.039 · Cited by 63
Wilson, E. B., Kidani, Y., Elsaesser, H. J., Barnard, J., Raff, L., Karp, C. L., Bensinger, S. J., & Brooks, D. G. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.03.009 · Cited by 64
The Expression of Tumor-Associated Macrophages in Papillary Thyroid Carcinoma
Kim, S., Cho, S. W., Min, H. S., Kim, K. M., Yeom, G. J., Kim, E. Y., Lee, K. E., Yun, Y. G., Park, D. J., & Park, Y. J. (2013) · Endocrinology and Metabolism · doi:10.3803/enm.2013.28.3.192 · Cited by 63
Mineralocorticoids in the Heart and Vasculature: New Insights for Old Hormones
Lother, A., Moser, M., Bode, C., Feldman, R. D., & Hein, L. (2014) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-010814-124302 · Cited by 65
MicroRNA regulation of macrophages in human pathologies
Wei, Y., & Schober, A. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2254-6 · Cited by 65
Geraniin Inhibits LPS-Induced THP-1 Macrophages Switching to M1 Phenotype via SOCS1/NF-κB Pathway
Liu, X., Li, J., Peng, X., Lv, B., Wang, P., Zhao, X., & Yu, B. (2016) · Inflammation · doi:10.1007/s10753-016-0374-7 · Cited by 63
Macrophage Polarization and Its Role in Cancer
Smith, E. W. C. (2015) · Journal of Clinical & Cellular Immunology · doi:10.4172/2155-9899.1000338 · Cited by 69
Li, L., Tao, Y., Feng, Z., Niu, Y., Tan, Q., Haowen, Z., Chen, Q., Jun, T., Zhang, Y., Gang, Z., et al. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00112 · Cited by 63
Disabled Homolog 2 Controls Prometastatic Activity of Tumor-Associated Macrophages
Marigo, I., Trovato, R., Hofer, F., Ingangi, V., Desantis, G., Leone, K., Sanctis, F. D., Ugel, S., Canè, S., Simonelli, A., et al. (2020) · Cancer Discovery · doi:10.1158/2159-8290.cd-20-0036 · Cited by 64
Won, H., Nandakumar, V., Yates, P., Sanchez, S., Jones, L. E., Huang, X. F., & Chen, S. (2014) · Blood · doi:10.1182/blood-2013-10-534313 · Cited by 62
Xue, J., Gao, J., Tang, A.-F., & Feng, C. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e37192 · Cited by 66
Chang, J., & Tang, C. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113056 · Cited by 66
Dong, R., Gong, Y., Meng, W., Meng, Y. G., Zhu, H., Ying, M., He, Q., Cao, J., & Yang, B. (2016) · Cancer Letters · doi:10.1016/j.canlet.2016.11.029 · Cited by 62
Promising landscape for regulating macrophage polarization: epigenetic viewpoint
Zhou, D., Yang, K., Chen, L., Zhang, W., Xu, Z., Zuo, J., Jiang, H., & Luan, J. (2017) · Oncotarget · doi:10.18632/oncotarget.17027 · Cited by 64
Heung, L. J., & Hohl, T. M. (2019) · PLoS Pathogens · doi:10.1371/journal.ppat.1007627 · Cited by 64
Wang, Q., Wei, S., Zhou, H., Shen, G., Gan, X., Zhou, S., Qiu, J., Shi, C., & Lu, L. (2019) · Cell Death Discovery · doi:10.1038/s41420-019-0198-y · Cited by 69
Roles of Macrophages and Exosomes in Liver Diseases
Shen, M., Shen, Y., Fan, X., Men, R., Ye, T., & Yang, L. (2020) · Frontiers in Medicine · doi:10.3389/fmed.2020.583691 · Cited by 61
The role of mechanobiology in progression of rotator cuff muscle atrophy and degeneration
Gibbons, M. C., Singh, A., Engler, A. J., & Ward, S. R. (2017) · Journal of Orthopaedic Research® · doi:10.1002/jor.23662 · Cited by 63
Macrophage Polarization Induced by Probiotic Bacteria: a Concise Review
Wang, Y., Liu, H., & Zhao, J. (2019) · Probiotics and Antimicrobial Proteins · doi:10.1007/s12602-019-09612-y · Cited by 62
Huang, L., Zhang, Y., Li, Y., Meng, F., Li, H., Zhang, H., Tu, J., Sun, C., & Luo, L. (2021) · Nano-Micro Letters · doi:10.1007/s40820-021-00647-x · Cited by 61
TREM2 Insufficiency Protects against Pulmonary Fibrosis by Inhibiting M2 Macrophage Polarization
Luo, Q., Deng, D., Li, Y., Shi, H., Zhao, J., Qian, Q., Wang, W., Cai, J., Yu, W., & Liu, J. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110070 · Cited by 64
Xiao, Y., Zijl, S., Wang, L., de Groot, D., van Tol, M. J., Lankester, A. C., & Borst, J. G. (2015) · Stem Cell Reports · doi:10.1016/j.stemcr.2015.04.012 · Cited by 63
Glezeva, N., Horgan, S. J., & Baugh, J. A. (2015) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2015.10.029 · Cited by 62
Hasegawa‐Moriyama, M., Ohnou, T., Godai, K., Kurimoto, T., Nakama, M., & Kanmura, Y. (2012) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.08.039 · Cited by 61
Ebola: translational science considerations
Chiappelli, F., Bakhordarian, A., Thames, A. D., Du, A. M., Jan, A. L., Nahcivan, M., Nguyen, M. T., Sama, N., Manfrini, E., Piva, F., et al. (2015) · Journal of Translational Medicine · doi:10.1186/s12967-014-0362-3 · Cited by 63
Epigenetic regulation of cellular functions in wound healing
Pastar, I., Marjanović, J., Stone, R. C., Chen, V., Burgess, J. L., Mervis, J. S., & Tomic‐Canic, M. (2021) · Experimental Dermatology · doi:10.1111/exd.14325 · Cited by 63
Troutman, T. D., Kofman, E. R., & Glass, C. K. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.08.004 · Cited by 62
The Importance of M1-and M2-Polarized Macrophages in Glioma and as Potential Treatment Targets
Ren, J., Xu, B., Ren, J., Liu, Z., Cai, L., Zhang, X., Wang, W., Li, S., Jin, L., & Ding, L. (2023) · Brain Sciences · doi:10.3390/brainsci13091269 · Cited by 63
Ndisang, J. F., & Jadhav, A. (2013) · Endocrinology · doi:10.1210/en.2013-1050 · Cited by 60
Chen, Y., Wang, S., Mu, R., Luo, X. G., Liu, Z.-S., Liang, B., Zhuo, H., Hao, X.-P., Wang, Q., Fang, D., et al. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.05.007 · Cited by 64
Zhang, Q., Bian, G., Chen, P., Liu, L., Yu, C., Liu, F., Xue, Q., Chung, S. K., Song, B., Ju, G., et al. (2014) · Molecular Neurobiology · doi:10.1007/s12035-014-9035-8 · Cited by 60
Mendoza, G., Regiel-Futyra, A., Andreu, V., Sebastián, V., Kyzioł, A., Stochel, G., & Arruebo, M. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b15123 · Cited by 60
Rojo, R., Pridans, C., Langlais, D., & Hume, D. A. (2017) · Clinical Science · doi:10.1042/cs20170238 · Cited by 66
M2-like polarization of THP-1 monocyte-derived macrophages under chronic iron overload
Kao, J., Wang, S., Ho, L.-W., Huang, S., Lee, C., Lee, M.-S., Yang, R., & Shieh, J. (2020) · Annals of Hematology · doi:10.1007/s00277-020-03916-8 · Cited by 61
Liu, C., Xu, Y., Lu, Y., Du, P., Li, X., Wang, C., Guo, P., Diao, L., & Lu, G. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-02934-9 · Cited by 59
Sharma, P., & Otto, M. (2023) · Bioactive Materials · doi:10.1016/j.bioactmat.2023.08.022 · Cited by 59
SEPTIN2 suppresses an IFN-γ-independent, proinflammatory macrophage activation pathway
Fu, B., Xiong, Y., Sha, Z., Xue, W., Xu, B., Tan, S., Guo, D., Lin, F., Wang, L., Ji, J., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43283-2 · Cited by 59
Lefèvre, L., Authier, H., Stein, S., Majorel, C., Couderc, B. C., Dardenne, C., Eddine, M. A., Meunier, É., Bernad, J., Valentin, A., et al. (2015) · Nature Communications · doi:10.1038/ncomms7801 · Cited by 59
Huber, R., Pietsch, D., Günther, J., Welz, B., Vogt, N., & Brand, K. (2013) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-013-1322-4 · Cited by 62
Prognostic value of diametrically polarized tumor-associated macrophages in multiple myeloma
Chen, X., Chen, J., Zhang, W., Sun, R., Liu, T., Zheng, Y., & Wu, Y. (2017) · Oncotarget · doi:10.18632/oncotarget.22340 · Cited by 59
Redox-signals and macrophage biology
Weigert, A., von Knethen, A., Fuhrmann, D. C., Dehne, N., & Brüne, B. (2018) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2018.01.003 · Cited by 60
The NADPH Oxidase Nox4 Controls Macrophage Polarization in an NFκB-Dependent Manner
Helfinger, V., Pálfi, K., Weigert, A., & Schröder, K. (2019) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2019/3264858 · Cited by 59
Liu, J., Lao, L., Chen, J., Jiang, L., Zeng, W., Zhu, X., Li, J., Chen, X., Yang, L., Xing, Y., et al. (2021) · Nature Cancer · doi:10.1038/s43018-021-00196-7 · Cited by 59
Wang, X., Zhao, W., Ransohoff, R. M., & Zhou, L. (2018) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2018.01.004 · Cited by 58
Yu, Y., Hu, Q., Liu, J., Su, A., Xu, H., Li, X., Huang, Q., Zhou, J., Mariga, A. M., & Yang, W. (2021) · Food and Chemical Toxicology · doi:10.1016/j.fct.2021.112111 · Cited by 58
Tollip Orchestrates Macrophage Polarization to Alleviate Intestinal Mucosal Inflammation
Liu, X., Ren, X., Zhou, L., Liu, K., Deng, L., Qing, Q., Li, J., Zhi, F., & Li, M. (2022) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjac019 · Cited by 60
Zhao, Z., Hou, X., Yin, X., Li, Y., Duan, R., Boyce, B. F., & Yao, Z. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135728 · Cited by 60
Mesenchymal stem cells-derived MFG-E8 accelerates diabetic cutaneous wound healing
Uchiyama, A., Motegi, S., Sekiguchi, A., Fujiwara, C., Perera, B., Ogino, S., Yokoyama, Y., & Ishikawa, O. (2017) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2017.02.285 · Cited by 58
Masola, V., Zaza, G., Bellin, G., Dall’Olmo, L., Granata, S., Vischini, G., Secchi, M. F., Lupo, A., Gambaro, G., & Onisto, M. (2017) · The FASEB Journal · doi:10.1096/fj.201700597r · Cited by 58
Chen, L., Zhang, J., Zou, Y., Wang, F., Li, J., Sun, F., Luo, X., Zhang, M., Guo, Y., Yu, Q., et al. (2021) · Cell Death and Differentiation · doi:10.1038/s41418-020-00714-7 · Cited by 58
Dániel, B., Czimmerer, Z., Halász, L., Botó, P., Kolostyák, Z., Póliska, S., Berger, W. K., Tzerpos, P., Nagy, G., Horváth, A., et al. (2020) · Genes & Development · doi:10.1101/gad.343038.120 · Cited by 58
Galectin-2 Induces a Proinflammatory, Anti-Arteriogenic Phenotype in Monocytes and Macrophages
Yıldırım, C., Vogel, D. Y. S., Hollander, M. R., Baggen, J. M. C., Fontijn, R. D., Nieuwenhuis, S., Haverkamp, A., de Vries, M. R., Quax, P. H. A., García-Vallejo, J. J., et al. (2015) · PLoS ONE · doi:10.1371/journal.pone.0124347 · Cited by 57
Spencer, M. L., Yang, L., Adu, A. K., Finlin, B. S., Zhu, B., Shipp, L. R., Rasouli, N., Peterson, C. A., & Kern, P. A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102190 · Cited by 59
Transcriptomic analysis of mononuclear phagocyte differentiation and activation
Hume, D. A., & Freeman, T. C. (2014) · Immunological Reviews · doi:10.1111/imr.12211 · Cited by 60
Patrick, C., Wang, G., Lefebvre, D. E., Crookshank, J. A., Sonier, B., Eberhard, C. E., Mojibian, M., Kennedy, C., Brooks, S. P. J., Kalmokoff, M. L., et al. (2013) · Diabetes · doi:10.2337/db12-1243 · Cited by 57
KLF6 contributes to myeloid cell plasticity in the pathogenesis of intestinal inflammation
Goodman, W. A., Omenetti, S., Date, D. A., Martino, L. D., Salvo, C. D., Kim, G. D., Chowdhry, S., Bamias, G., Cominelli, F., Pizarro, T. T., et al. (2016) · Mucosal Immunology · doi:10.1038/mi.2016.1 · Cited by 57
Ren, C.-X., Leng, R., Fan, Y., Pan, H., Li, B., Wu, C., Wu, Q., Wang, N., Xiong, Q., Geng, X., et al. (2017) · Oncology Reports · doi:10.3892/or.2017.5738 · Cited by 57
Monocytes and the Host Response to Fungal Pathogens
Heung, L. J. (2020) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2020.00034 · Cited by 60
Improved Angiogenesis in Response to Localized Delivery of Macrophage-Recruiting Molecules
Hsu, C.-W., Poché, R. A., Saik, J. E., Ali, S., Wang, S., Yosef, N., Calderon, G. A., Scott, L., Vadakkan, T. J., Larina, I. V., et al. (2015) · PLOS ONE · doi:10.1371/journal.pone.0131643 · Cited by 56
Cui, H., Banerjee, S., Guo, S., Xie, N., & Liu, G. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701571 · Cited by 56
Ni, C., Jiang, W., Wang, Z., Wang, Z., Zhang, J., Zheng, X., Liu, Z., Ou, H., Jiang, T., Liang, W., et al. (2020) · Molecular Psychiatry · doi:10.1038/s41380-020-0662-3 · Cited by 58
MiR-19a-3p Suppresses M1 Macrophage Polarization by Inhibiting STAT1/IRF1 Pathway
Zhu, X., Guo, Q., Zou, J., Wang, B., Zhang, Z., Wei, R., Zhao, L., Zhang, Y., Chu, C., Fu, X., et al. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.614044 · Cited by 56
Guido, G., Ausenda, G., Iascone, V., & Chisari, E. (2021) · Annals of Medicine · doi:10.1080/07853890.2021.2014557 · Cited by 62
Zheng, Y., Ren, S., Zhang, Y., Liu, S., Meng, L., Liu, F., Gu, L., Ai, N., & Sang, M. (2022) · Cancer Cell International · doi:10.1186/s12935-022-02686-9 · Cited by 56
Zhang, G., Lü, J., Zheng, J., Mei, S., Li, H., Zhang, X., Ping, A., Gao, S., Fang, Y., & Yu, J. (2023) · Neural Regeneration Research · doi:10.4103/1673-5374.375343 · Cited by 58
The Involvement of Neuroinflammation in the Onset and Progression of Parkinson’s Disease
Jurcău, A., Andronie-Cioară, F. L., Nistor-Cseppento, C. D., Pașcalău, N., Rus, M., Vasca, E., & Jurcău, M. C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914582 · Cited by 58
Bhatt, M., Sharma, M., & Das, B. (2024) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-024-01519-9 · Cited by 62
Pentamethoxyflavanone regulates macrophage polarization and ameliorates sepsis in mice
Feng, L., Song, P., Zhou, H., Li, A., Ma, Y., Zhang, X., Liu, H., Xu, G., Zhou, Y., Wu, X., et al. (2014) · Biochemical Pharmacology · doi:10.1016/j.bcp.2014.02.016 · Cited by 56
Li, S., Wang, W., Fu, S., Wang, J., Liu, H., Xie, S., Liu, B.-R., Li, Y., Lv, Q.-K., Li, Z., et al. (2013) · Mediators of Inflammation · doi:10.1155/2013/548073 · Cited by 59
LPS-induced NFκB enhanceosome requires TonEBP/NFAT5 without DNA binding
Lee, H. H., Sanada, S., An, S. M., Ye, B. J., Lee, J. H., Seo, Y., Lee, C., Lee‐Kwon, W., Küper, C., Neuhofer, W., et al. (2016) · Scientific Reports · doi:10.1038/srep24921 · Cited by 58
Metadata
- Authors
- Lawrence, T., & Natoli, G.
- Affiliations
- Centre d’Immunologie de Marseille-Luminy (FR)
- European Institute of Oncology (IT)
- Corresponding author
- Lawrence, Toby
- Natoli, Gioacchino
- Venue
- Nature Reviews Immunology
- Published
- 2011-10-25
- Volume
- 11
- Issue
- 11
- Pages
- 750-761
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- OpenAlex
- W2081810806
- Cited by
- 2,284
- References
- 90
- Citations by year
- 2026: 124 · 2025: 147 · 2024: 194 · 2023: 180 · 2022: 190 · 2021: 203 · 2020: 158 · 2019: 139 · 2018: 149 · 2017: 166 · 2016: 165 · 2015: 158 · 2014: 140 · 2013: 108 · 2012: 58
- FWCI
- 8.84
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Agence Nationale de la Recherche
- Institut National de la Santé et de la Recherche Médicale
- Centre National de la Recherche Scientifique
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Peroxisome Proliferator-Activated Receptors
- Keywords
- macrophage polarization, macrophage identity, transcription factors, chromatin regulation, macrophage heterogeneity, tissue-resident macrophages, macrophage differentiation, macrophage lineage
- MeSH terms
- Interferon Regulatory Factor-4, Gene Expression Regulation, Humans, Macrophages, Promoter Regions, Genetic, Protein Binding, PPAR gamma, STAT1 Transcription Factor, STAT6 Transcription Factor, Interferon Regulatory Factors
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