Origin and Functions of Tissue Macrophages

Copper-Zinc Superoxide Dismutase (SOD1) Is Released by Microglial Cells and Confers Neuroprotection against 6-OHDA Neurotoxicity

Polazzi, E., Mengoni, I., Caprini, M., Peña‐Altamira, E., Kurtys, E., & Monti, B. (2012) · Neurosignals · doi:10.1159/000337115 · Cited by 9,023

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

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

Macrophage 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×

Synaptic Pruning by Microglia Is Necessary for Normal Brain Development

Paolicelli, R. C., Bolasco, G., Pagani, F., Maggi, L., Scianni, M., Panzanelli, P., Giustetto, M., Ferreira, T. A., Guiducci, E., Dumas, L., et al. (2011) · Science · doi:10.1126/science.1202529 · Cited by 4,244

The Classical Complement Cascade Mediates CNS Synapse Elimination

Stevens, B., Allen, N. J., Vazquez, L. E., Howell, G. R., Christopherson, K. S., Nouri, N., Micheva, K. D., Mehalow, A. K., Huberman, A. D., Stafford, B., et al. (2007) · Cell · doi:10.1016/j.cell.2007.10.036 · Cited by 3,313

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

TREM2 Variants in Alzheimer's Disease

Guerreiro, R., Wojtas, A., Bras, J., Carrasquillo, M., Rogaeva, E., Majounie, E., Cruchaga, C., Sassi, C., Kauwe, J. S. K., Younkin, S., et al. (2013) · New England Journal of Medicine · doi:10.1056/nejmoa1211851 · Cited by 3,020

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

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

Microglia promote learning-dependent synapse formation through brain-derived neurotrophic factor

Parkhurst, C. N., Yang, G., Ninan, I., Savas, J. N., Yates, J. R., Lafaille, J. J., Hempstead, B. L., Littman, D. R., & Gan, W.-B. (2013) · Cell · doi:10.1016/j.cell.2013.11.030 · Cited by 2,599

Innate Immune Responses to Tuberculosis

Schorey, J. S., & Schlesinger, L. S. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.tbtb2-0010-2016 · Cited by 125

Lifestyle Effects on Hematopoiesis and Atherosclerosis

Nahrendorf, M., & Świrski, F. K. (2015) · Circulation Research · doi:10.1161/circresaha.116.303550 · Cited by 124

Mesenchymal Stem Cell-Derived Extracellular Vesicles: A Novel Cell-Free Therapy

Jafarinia, M., Alsahebfosoul, F., Salehi, H., Eskandari, N., & Ganjalıkhani-Hakemi, M. (2020) · Immunological Investigations · doi:10.1080/08820139.2020.1712416 · Cited by 124

The Role of Macrophages in the Infarcted Myocardium: Orchestrators of ECM Remodeling

O’Rourke, S. A., Dunne, A., & Monaghan, M. G. (2019) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2019.00101 · Cited by 124

Distinct fate, dynamics and niches of renal macrophages of bone marrow or embryonic origins

Liu, F., Dai, S., Feng, D., Qin, Z., Peng, X., Sakamuri, S. S. V. P., Ren, M., Huang, L., Cheng, M., Mohammad, K. E., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-16158-z · Cited by 130

The Origins and Functions of Tissue-Resident Macrophages in Kidney Development

Munro, D. A. D., & Hughes, J. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00837 · Cited by 124

Multinucleated Giant Cells: Current Insights in Phenotype, Biological Activities, and Mechanism of Formation

Ahmadzadeh, K., Vanoppen, M., Rosé, C. D., Matthys, P., & Wouters, C. H. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.873226 · Cited by 127

Maresin 1 attenuates neuroinflammation in a mouse model of perioperative neurocognitive disorders

Yang, T., Xu, G., Newton, P. T., Chagin, A. S., Mkrtchian, S., Carlström, M., Zhang, X., Harris, R. A., Cooter, M. L., Berger, M., et al. (2018) · British Journal of Anaesthesia · doi:10.1016/j.bja.2018.10.062 · Cited by 119

Why Innate Lymphoid Cells?

Kotas, M. E., & Locksley, R. M. (2018) · Immunity · doi:10.1016/j.immuni.2018.06.002 · Cited by 123

Harnessing Expressed Single Nucleotide Variation and Single Cell RNA Sequencing To Define Immune Cell Chimerism in the Rejecting Kidney Transplant

Malone, A. F., Wu, H., Fronick, C. C., Fulton, R. S., Gaut, J. P., & Humphreys, B. D. (2020) · Journal of the American Society of Nephrology · doi:10.1681/asn.2020030326 · Cited by 119

Monocytes and macrophages: Origin, homing, differentiation, and functionality during inflammation

Dash, S. P., Gupta, S., & Sarangi, P. P. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e29686 · Cited by 124

Forced Activation of Notch in Macrophages Represses Tumor Growth by Upregulating miR-125a and Disabling Tumor-Associated Macrophages

Zhao, J., Huang, F., He, F., Gao, C.-C., Liang, S.-Q., Ma, P., Dong, G., Han, H., & Qin, H. (2016) · Cancer Research · doi:10.1158/0008-5472.can-15-2019 · Cited by 115

Tumor microenvironment and immunotherapy of oral cancer

Liu, C. X., Wang, M., Zhang, H., Li, C., Zhang, T., Liu, H. S., Zhu, S., & Chen, J. (2022) · European journal of medical research · doi:10.1186/s40001-022-00835-4 · Cited by 124

Chasing the recipe for a pro-regenerative immune system

Godwin, J. W., Pinto, A. R., & Rosenthal, N. A. (2016) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2016.08.008 · Cited by 117

Neutrophils and Macrophages as Targets for Development of Nanotherapeutics in Inflammatory Diseases

Su, Y., Gao, J., Kaur, P., & Wang, Z. (2020) · Pharmaceutics · doi:10.3390/pharmaceutics12121222 · Cited by 120

Macrophages in myocardial infarction

Kubota, A., & Frangogiannis, N. G. (2022) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00230.2022 · Cited by 123

Functions and development of red pulp macrophages

Kurotaki, D., Uede, T., & Tamura, T. (2015) · Microbiology and Immunology · doi:10.1111/1348-0421.12228 · Cited by 121

Ly6Chigh Monocytes Control Cerebral Toxoplasmosis

Biswas, A., Bruder, D., Wolf, S. A., Jeron, A., Mack, M., Heimesaat, M. M., & Dunay, I. R. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402037 · Cited by 115

Notch Signaling Modulates Macrophage Polarization and Phagocytosis Through Direct Suppression of Signal Regulatory Protein α Expression

Yan, L., Zhao, J., Zheng, Q., Jiang, X., Tian, J., Liang, S.-Q., Guo, H., Qin, H., Liang, Y., & Han, H. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01744 · Cited by 113

Resident Innate Immune Cells in the Cornea

Liu, J., & Li, Z. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.620284 · Cited by 114

Vascularized Polypeptide Hydrogel Modulates Macrophage Polarization for Wound Healing

Chen, Z., Wang, L., Guo, C., Qiu, M., Cheng, L., Chen, K., Qi, J., Deng, L., He, C., Li, X., et al. (2022) · Acta Biomaterialia · doi:10.1016/j.actbio.2022.11.002 · Cited by 111

Nanomedicine Strategies to Target Tumor-Associated Macrophages

Binnemars‐Postma, K., Storm, G., & Prakash, J. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18050979 · Cited by 112

Astragaloside IV Alleviates the Experimental DSS-Induced Colitis by Remodeling Macrophage Polarization Through STAT Signaling

Tian, L., Zhao, J., Kang, J., Guo, S., Zhang, N., Shang, L., Zhang, Y., Zhang, J., Jiang, X., & Yan, L. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.740565 · Cited by 109

Heterogeneous origins and functions of mouse skeletal muscle-resident macrophages

Wang, X., Sathe, A. A., Smith, G. R., Ruf-Zamojski, F. M., Nair, V., Lavine, K. J., Xing, C., Sealfon, S. C., & Zhou, L. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1915950117 · Cited by 120

Understanding the Biology of Self-Renewing Macrophages

Rőszer, T. (2018) · Cells · doi:10.3390/cells7080103 · Cited by 115

Pathogenic stromal cells as therapeutic targets in joint inflammation

Dakin, S. G., Coles, M. C., Sherlock, J. P., Powrie, F. M., Carr, A. J., & Buckley, C. D. (2018) · Nature Reviews Rheumatology · doi:10.1038/s41584-018-0112-7 · Cited by 107

Role of inflammatory cells in fibroblast activation

Hartupee, J. C., & Mann, D. L. (2015) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2015.11.016 · Cited by 110

NOTCH Signaling via WNT Regulates the Proliferation of Alternative, CCR2-Independent Tumor-Associated Macrophages in Hepatocellular Carcinoma

Ye, Y., Zhao, J., Lu, Y., Gao, C.-C., Yang, Y., Liang, S.-Q., Lu, Y., Wang, L., Yue, S., Dou, K., et al. (2019) · Cancer Research · doi:10.1158/0008-5472.can-18-1691 · Cited by 107

Role of the Monocyte–Macrophage System in Normal Pregnancy and Preeclampsia

Vishnyakova, P., Elchaninov, A. V., Fatkhudinov, T., & Sukhikh, G. T. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20153695 · Cited by 106

Modifiable Cardiovascular Risk, Hematopoiesis, and Innate Immunity

Schloss, M. J., Świrski, F. K., & Nahrendorf, M. (2020) · Circulation Research · doi:10.1161/circresaha.120.315936 · Cited by 114

Kidney-resident macrophages promote a proangiogenic environment in the normal and chronically ischemic mouse kidney

Puranik, A. S., Leaf, I. A., Jensen, M. A., Hedayat, A. F., Saad, A., Kim, K.-W., Saadalla, A. M., Woollard, J. R., Kashyap, S., Textor, S. C., et al. (2018) · Scientific Reports · doi:10.1038/s41598-018-31887-4 · Cited by 109

Immune cells in liver regeneration

Li, N., & Hua, J. (2017) · Oncotarget · doi:10.18632/oncotarget.12275 · Cited by 104

The macrophages in testis function

Bhushan, S., & Meinhardt, A. (2016) · Journal of Reproductive Immunology · doi:10.1016/j.jri.2016.06.008 · Cited by 104

Macrophage Heterogeneity in Kidney Injury and Fibrosis

Wen, Y., Yan, H.-R., Wang, B., & Liu, B. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.681748 · Cited by 102

Hacking the host: exploitation of macrophage polarization by intracellular bacterial pathogens

Thiriot, J. D., Martinez-Martinez, Y. B., Endsley, J. J., & Torres, A. G. (2020) · Pathogens and Disease · doi:10.1093/femspd/ftaa009 · Cited by 103

Glucocorticoids Shape Macrophage Phenotype for Tissue Repair

Desgeorges, T., Caratti, G., Mounier, R., Tuckermann, J. P., & Chazaud, B. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.01591 · Cited by 109

Chemokines in Myocardial Infarction

Chen, B., & Frangogiannis, N. G. (2020) · Journal of Cardiovascular Translational Research · doi:10.1007/s12265-020-10006-7 · Cited by 104

Resident tissue macrophages: Key coordinators of tissue homeostasis beyond immunity

Zhao, J., Andreev, I., & Silva, H. M. (2024) · Science Immunology · doi:10.1126/sciimmunol.add1967 · Cited by 109

Myocardial Galectin-3 Expression Is Associated with Remodeling of the Pressure-Overloaded Heart and May Delay the Hypertrophic Response without Affecting Survival, Dysfunction, and Cardiac Fibrosis

Frunza, O., Russo, I., Saxena, A., Shinde, A. V., Humeres, C. D., Hanif, W., Rai, V., Su, Y., & Frangogiannis, N. G. (2016) · American Journal Of Pathology · doi:10.1016/j.ajpath.2015.12.017 · Cited by 102

Interactions with the macrophages: An emerging targeted approach using novel drug delivery systems in respiratory diseases

Mehta, M., Deeksha, Sharma, N., Vyas, M., Khurana, N., Maurya, P. K., Singh, H., de Jesus, T. P. A., Dureja, H., Chellappan, D. K., et al. (2019) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2019.02.021 · Cited by 101

New Insights From Single-Cell Sequencing Data: Synovial Fibroblasts and Synovial Macrophages in Rheumatoid Arthritis

Cheng, L., Wang, Y., Wu, R., Ding, T., Xue, H., Gao, C., Li, X., & Wang, C. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.709178 · Cited by 102

The macrophage: a key player in the pathophysiology of peripheral neuropathies

Msheik, Z., Massry, M. E., Rovini, A. M. F., Billet, F., & Desmoulière, A. (2022) · Journal of Neuroinflammation · doi:10.1186/s12974-022-02454-6 · Cited by 108

Quercetin alleviates ferroptosis accompanied by reducing M1 macrophage polarization during neutrophilic airway inflammation

Wang, Y., Wan, R., Wang, P., Li, Y., Zhao, X., Bai, W., Chen, Q., & Hu, C. (2022) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2022.175407 · Cited by 106

Epithelium- and endothelium-derived exosomes regulate the alveolar macrophages by targeting RGS1 mediated calcium signaling-dependent immune response

Feng, Z., Zhou, J., Liu, Y., Xia, R., Li, Q., Yan, L., Chen, Q., Chen, X., Jiang, Y., Gao, C., et al. (2021) · Cell Death and Differentiation · doi:10.1038/s41418-021-00750-x · Cited by 106

Occurrences and Functions of Ly6Chi and Ly6Clo Macrophages in Health and Disease

Li, Y., Zhang, Y., Pan, G., Xiang, L., Luo, D., & Shao, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.901672 · Cited by 109

Systemic and Cardiac Depletion of M2 Macrophage through CSF-1R Signaling Inhibition Alters Cardiac Function Post Myocardial Infarction

Leblond, A., Klinkert, K., Martin, K., Turner, E. C., Kumar, A. H. S., Browne, T. C., & Caplice, N. M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0137515 · Cited by 103

Essential Oils and Their Major Compounds in the Treatment of Chronic Inflammation: A Review of Antioxidant Potential in Preclinical Studies and Molecular Mechanisms

de Lavor, É. M., Fernandes, A. W. C., Teles, R. B. D. A., Leal, A. E. B. P., Júnior, R. G. D. O., Silva, M. G. E., de Oliveira, A. P., Silva, J. C., Araújo, M. T. D. M. F., Coutinho, H. D. M., et al. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/6468593 · Cited by 103

Engineering nanoparticles to overcome immunological barriers for enhanced drug delivery

Malachowski, T., & Hassel, A. (2020) · Engineered Regeneration · doi:10.1016/j.engreg.2020.06.001 · Cited by 99

Human anti-PSCA CAR macrophages possess potent antitumor activity against pancreatic cancer

Shah, Z., Tian, L., Li, Z., Jin, L., Zhang, J., Li, Z., Barr, T., Tang, H., Feng, M., Caligiuri, M. A., et al. (2024) · Cell stem cell · doi:10.1016/j.stem.2024.03.018 · Cited by 107

Immunomodulatory Therapeutic Effects of Curcumin on M1/M2 Macrophage Polarization in Inflammatory Diseases

Azhdari, S., Moghaddam, A. S., Abdollahi, E., Johnston, T. P., Ghaneifar, Z., Vahedi, P., & Goleij, P. (2022) · Current Molecular Pharmacology · doi:10.2174/1874467215666220324114624 · Cited by 99

Alveolar Macrophages in Allergic Asthma: the Forgotten Cell Awakes

Draijer, C., & Peters-Golden, M. L. (2017) · Current Allergy and Asthma Reports · doi:10.1007/s11882-017-0681-6 · Cited by 95

The Role of Myeloid-Derived Cells in the Progression of Liver Disease

Weston, C. J., Zimmermann, H. W., & Adams, D. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00893 · Cited by 92

Therapeutic Potential of Hematopoietic Prostaglandin D2 Synthase in Allergic Inflammation

Rittchen, S., & Heinemann, Á. (2019) · Cells · doi:10.3390/cells8060619 · Cited by 95

Peripheral monocyte-derived cells counter amyloid plaque pathogenesis in a mouse model of Alzheimer’s disease

Yan, P., Kim, K.-W., Xiao, Q., Ma, X., Czerniewski, L. R., Liu, H., Rawnsley, D. R., Yan, Y., Randolph, G. J., Epelman, S., et al. (2022) · Journal of Clinical Investigation · doi:10.1172/jci152565 · Cited by 95

GM-CSF primes cardiac inflammation in a mouse model of Kawasaki disease

Stock, A. T., Hansen, J. A., Sleeman, M. A., McKenzie, B. S., & Wicks, I. P. (2016) · The Journal of Experimental Medicine · doi:10.1084/jem.20151853 · Cited by 92

Skeletal muscle inflammation and atrophy in heart failure

Lavine, K. J., & Sierra, O. L. (2017) · Heart Failure Reviews · doi:10.1007/s10741-016-9593-0 · Cited by 96

Alcohol, aging, and innate immunity

Boulé, L. A., & Kovacs, E. J. (2017) · Journal of Leukocyte Biology · doi:10.1189/jlb.4ru1016-450r · Cited by 94

The epigenetic state of IL-4-polarized macrophages enables inflammatory cistromic expansion and extended synergistic response to TLR ligands

Czimmerer, Z., Halász, L., Dániel, B., Varga, Z., Bene, K., Domokos, A., Hoeksema, M. A., Shen, Z., Berger, W. K., Cseh, T., et al. (2022) · Immunity · doi:10.1016/j.immuni.2022.10.004 · Cited by 92

Single-cell profiling of healthy human kidney reveals features of sex-based transcriptional programs and tissue-specific immunity

McEvoy, C. M., Murphy, J. M., Zhang, L., Clotet‐Freixas, S., Mathews, J. A., An, J., Karimzadeh, M., Pouyabahar, D., Su, S., Zaslaver, O., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-35297-z · Cited by 93

Influences of innate immunity, autophagy, and fibroblast activation in the pathogenesis of lung fibrosis

O’Dwyer, D. N., Ashley, S. L., & Moore, B. B. (2016) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00221.2016 · Cited by 90

The origins and non-canonical functions of macrophages in development and regeneration

Théret, M., Mounier, R., & Rossi, F. M. V. (2019) · Development · doi:10.1242/dev.156000 · Cited by 90

Local sympathetic innervations modulate the lung innate immune responses

Liu, T., Yang, L., Han, X., Ding, X., Li, J., & Yang, J. H. (2020) · Science Advances · doi:10.1126/sciadv.aay1497 · Cited by 89

cGAS-STING pathway as a potential trigger of immunosenescence and inflammaging

Schmitz, C. R. R., Maurmann, R. M., Guma, F. T. C. R., Bauer, M. E., & Barbé‐Tuana, F. M. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1132653 · Cited by 95

M2 Macrophages Enhance Pathological Neovascularization in the Mouse Model of Oxygen-Induced Retinopathy

Zhou, Y., Yoshida, S., Nakao, S., Yoshimura, T., Kobayashi, Y., Nakama, T., Kubo, Y., Miyawaki, K., Yamaguchi, M., Ishikawa, K., et al. (2015) · Investigative Ophthalmology & Visual Science · doi:10.1167/iovs.14-16012 · Cited by 87

Macrophage function in the elderly and impact on injury repair and cancer

Duong, L., Radley‐Crabb, H. G., Lee, B. R., Dye, D. E., Pixley, F. J., Grounds, M. D., Nelson, D. J., & Jackaman, C. (2021) · Immunity & Ageing · doi:10.1186/s12979-021-00215-2 · Cited by 93

Brazilian Red Propolis Attenuates Inflammatory Signaling Cascade in LPS-Activated Macrophages

Bueno‐Silva, B., Kawamoto, D., Ando‐Suguimoto, E. S., de Alencar, S. M., Rosalen, P. L., & Mayer, M. P. A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0144954 · Cited by 91

Tissue-Resident Macrophages in the Control of Infection and Resolution of Inflammation

Mu, X., Li, Y., & Fan, G. (2020) · Shock · doi:10.1097/shk.0000000000001601 · Cited by 93

IL-33-ST2 axis regulates myeloid cell differentiation and activation enabling effective club cell regeneration

Dagher, R., Copenhaver, A. M., Besnard, V., Berlin, A. A., Hamidi, F., Maret, M., Wang, J., Qu, X., Shrestha, Y., Wu, J., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18466-w · Cited by 89

The Role of Pancreatic Infiltrating Innate Immune Cells in Acute Pancreatitis

Peng, C., Li, Z., & Yu, X. (2020) · International Journal of Medical Sciences · doi:10.7150/ijms.51618 · Cited by 90

Aging dysregulates D- and E-series resolvins to modulate cardiosplenic and cardiorenal network following myocardial infarction

Halade, G. V., Kain, V., Black, L. M., Prabhu, S. D., & Ingle, K. A. (2016) · Aging · doi:10.18632/aging.101077 · Cited by 83

Androgen and Androgen Receptors as Regulators of Monocyte and Macrophage Biology in the Healthy and Diseased Lung

Becerra-Díaz, M., Song, M., & Heller, N. M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01698 · Cited by 89

New Insights and Novel Therapeutic Potentials for Macrophages in Myocardial Infarction

Zhang, Z., Tang, J., Cui, X., Qin, B., Zhang, J., Zhang, H., Zhang, H., Liu, G., Wang, W., & Zhang, J. (2021) · Inflammation · doi:10.1007/s10753-021-01467-2 · Cited by 86

Kupffer cell receptor CLEC4F is important for the destruction of desialylated platelets in mice

Jiang, Y., Tang, Y., Hoover, C., Kondo, Y., Huang, D., Restagno, D., Shao, B., Gao, L., McDaniel, J. M., Zhou, M., et al. (2021) · Cell Death and Differentiation · doi:10.1038/s41418-021-00797-w · Cited by 84

Overview of the immunological mechanism underlying severe fever with thrombocytopenia syndrome (Review)

Yang, T., Huang, H., Jiang, L., & Li, J. (2022) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2022.5174 · Cited by 84

Immune and inflammatory responses of human macrophages, dendritic cells, and T-cells in presence of micro- and nanoplastic of different types and sizes

Wolff, C. M., Singer, D., Schmidt, A., & Bekeschus, S. (2023) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2023.132194 · Cited by 92

The Complex Myeloid Network of the Liver with Diverse Functional Capacity at Steady State and in Inflammation

Eckert, C., Klein, N., Kornek, M., & Kornek, M. (2015) · Frontiers in Immunology · doi:10.3389/fimmu.2015.00179 · Cited by 84

MAFB Determines Human Macrophage Anti-Inflammatory Polarization: Relevance for the Pathogenic Mechanisms Operating in Multicentric Carpotarsal Osteolysis

Cuevas, V. D., Anta, L., Samaniego, R., Orta-Zavalza, E., Vladimir de la Rosa, J., Baujat, G., Domínguez-Soto, Á., Sánchez-Mateos, P., Escribese, M. M., Castrillo, A., et al. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601667 · Cited by 82

Distinct microenvironmental cues stimulate divergent TLR4-mediated signaling pathways in macrophages

Piccinini, A. M., Zuliani‐Alvarez, L., Lim, J. M. P., & Midwood, K. S. (2016) · Science Signaling · doi:10.1126/scisignal.aaf3596 · Cited by 82

Donor Macrophages Modulate Rejection After Heart Transplantation

Kopecky, B. J., Dun, H., Amrute, J., Lin, C., Bredemeyer, A. L., Terada, Y., Bayguinov, P. O., Koenig, A. L., Frye, C. C., Fitzpatrick, J. A. J., et al. (2022) · Circulation · doi:10.1161/circulationaha.121.057400 · Cited by 81

Origin and Heterogeneity of Tissue Myeloid Cells: A Focus on GMP-Derived Monocytes and Neutrophils

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Tumor location determines tissue-specific recruitment of tumor-associated macrophages and antibody-dependent immunotherapy response

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