Monocytes and macrophages: developmental pathways and tissue homeostasis

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

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

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

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

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

Hematopoiesis: An Evolving Paradigm for Stem Cell Biology

Orkin, S. H., & Zon, L. I. (2008) · Cell · doi:10.1016/j.cell.2008.01.025 · Cited by 2,570

Tissue-Resident Macrophages Self-Maintain Locally throughout Adult Life with Minimal Contribution from Circulating Monocytes

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

Identification of splenic reservoir monocytes and their deployment to inflammatory sites

Swirski, F. K., Nahrendorf, M., Etzrodt, M., Wildgruber, M., Cortez-Retamozo, V., Panizzi, P., Figueiredo, J.-L., Kohler, R. H., Chudnovskiy, A., Waterman, P., et al. (2009) · Science · doi:10.1126/science.1175202 · Cited by 2,221

Pericytes are required for blood–brain barrier integrity during embryogenesis

Daneman, R., Zhou, L., Kebede, A. A., & Barres, B. A. (2010) · Nature · doi:10.1038/nature09513 · Cited by 2,128

Alveolar Macrophages: Adaptation to Their Anatomic Niche during and after Inflammation

Martin, F. P., Jacqueline, C., Poschmann, J., & Roquilly, A. (2021) · Cells · doi:10.3390/cells10102720 · Cited by 56

The roles of tissue resident macrophages in health and cancer

Cao, M., Wang, Z., Lan, W., Xiang, B., Liao, W., Zhou, J., Liu, X., Wang, Y., Zhang, S., Lu, S., et al. (2024) · Experimental Hematology and Oncology · doi:10.1186/s40164-023-00469-0 · Cited by 59

Self-Adapting Biomass Hydrogel Embodied with miRNA Immunoregulation and Long-Term Bacterial Eradiation for Synergistic Chronic Wound Therapy

Wu, J., Wu, Y., Tang, H., Li, W., Zhao, Z., Shi, X., Jiang, H., Yu, L., & Deng, H. (2024) · ACS Nano · doi:10.1021/acsnano.4c02736 · Cited by 56

Single-cell analysis identifies distinct macrophage phenotypes associated with prodisease and proresolving functions in the endometriotic niche

Henlon, Y., Panir, K., McIntyre, I., Hogg, C., Dhami, P., Cuff, A. O., Senior, A., Moolchandani-Adwani, N., Courtois, E. T., Horne, A. W., et al. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2405474121 · Cited by 56

Impaired activation of ALS monocytes by exosomes

Zondler, L., Feiler, M. S., Freischmidt, A., Ruf, W. P., Ludolph, A. C., Danzer, K. M., & Weishaupt, J. H. (2016) · Immunology and Cell Biology · doi:10.1038/icb.2016.89 · Cited by 57

A monocyte gene expression signature in the early clinical course of Parkinson’s disease

Schlachetzki, J. C. M., Prots, I., Tao, J., Chun, H. B., Saijo, K., Gosselin, D., Winner, B., Glass, C. K., & Winkler, J. (2018) · Scientific Reports · doi:10.1038/s41598-018-28986-7 · Cited by 58

Neutrophil-mediated transport is crucial for delivery of short-circulating magnetic nanoparticles to tumors

Naumenko, V., Nikitin, A. A., Garanina, A. S., Melnikov, P., Vodopyanov, S., Kapitanova, K., Potashnikova, D. M., Vishnevskiy, D. A., Alieva, I. B., Iliasov, A., et al. (2020) · Acta Biomaterialia · doi:10.1016/j.actbio.2020.01.011 · Cited by 57

IFN-γ Drives Human Monocyte Differentiation into Highly Proinflammatory Macrophages That Resemble a Phenotype Relevant to Psoriasis

Luque-Martin, R., Angell, D. C., Kalxdorf, M., Bernard, S. G., Thompson, W., Eberl, H. C., Ashby, C. A., Freudenberg, J., Sharp, C. H., den Bossche, J. V., et al. (2021) · The Journal of Immunology · doi:10.4049/jimmunol.2001310 · Cited by 57

Ly6C- Monocytes Regulate Parasite-Induced Liver Inflammation by Inducing the Differentiation of Pathogenic Ly6C+ Monocytes into Macrophages

Morias, Y., Abels, C., Laoui, D., Overmeire, E. V., Guilliams, M., Schouppe, E., Tacke, F., de Vries, C. J. M., BAETSELIER, P. D., & Beschin, A. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1004873 · Cited by 54

The advantageous role of annexin A1 in cardiovascular disease

de Jong, R., Leoni, G., Drechsler, M. D., & Soehnlein, O. (2016) · Cell Adhesion & Migration · doi:10.1080/19336918.2016.1259059 · Cited by 55

Critical roles of mTORC1 signaling and metabolic reprogramming for M-CSF–mediated myelopoiesis

Karmaus, P. W. F., Herrada, A. A., Guy, C. S., Neale, G. A. M., Dhungana, Y., Long, L., Vogel, P., Ávila-Pacheco, J., Clish, C. B., & Chi, H. (2017) · The Journal of Experimental Medicine · doi:10.1084/jem.20161855 · Cited by 58

Endocytosis as a stabilizing mechanism for tissue homeostasis

Adler, M., Mayo, A., Zhou, X., Franklin, R. A., Jacox, J. B., Medzhitov, R. M., & Alon, U. S. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714377115 · Cited by 52

Bioactive Materials: A Comprehensive Review on Interactions with Biological Microenvironment Based on the Immune Response

Nour, S., Baheiraei, N., Imani, R., Rabiee, N., Khodaei, M., Alizadeh, A., & Moazzeni, S. M. (2019) · Journal of Bionic Engineering · doi:10.1007/s42235-019-0046-z · Cited by 55

Enhancement of Th1/Th17 inflammation by TRIM21 in Behçet’s disease

Ahn, Y., Hwang, J., Zheng, Z., Bang, D., & ‍Kim, D. Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-03251-5 · Cited by 54

Nanoparticle-Mediated Delivery of Pitavastatin to Monocytes/Macrophages Inhibits Left Ventricular Remodeling After Acute Myocardial Infarction by Inhibiting Monocyte-Mediated Inflammation

Mao, Y., Koga, J., Tokutome, M., Matoba, T., Ikeda, G., Nakano, K., & Egashira, K. (2017) · International Heart Journal · doi:10.1536/ihj.16-457 · Cited by 55

Microglia and Microglia-Like Cells: Similar but Different

Cuadros, M. Á., Sepúlveda, M. R., Martín‐Oliva, D., Marín‐Teva, J. L., & Neubrand, V. E. (2022) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2022.816439 · Cited by 57

Methyl CpG binding protein 2 deficiency enhances expression of inflammatory cytokines by sustaining NF-κB signaling in myeloid derived cells

O’Driscoll, C. M., Palma-Lima, M., Kaufmann, W. E., & Bressler, J. P. (2015) · Journal of Neuroimmunology · doi:10.1016/j.jneuroim.2015.04.005 · Cited by 55

Identification of differentially methylated BRCA1 and CRISP2 DNA regions as blood surrogate markers for cardiovascular disease

Istas, G., Declerck, K., Pudenz, M., Szic, K. S. V., Lendinez-Tortajada, V., León-Latre, M., Heyninck, K., Haegeman, G., Casasnovas, J. A., Téllez-Plaza, M., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-03434-0 · Cited by 53

Recent advances in the understanding of microglial development and homeostasis

Low, D., & Ginhoux, F. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.01.004 · Cited by 57

Proinflammatory Differentiation of Macrophages Through Microparticles That Form Immune Complexes Leads to T- and B-Cell Activation in Systemic Autoimmune Diseases

Burbano, C., Villar-Vesga, J., Vásquez, G. M., Muñoz‐Vahos, C. H., Rojas, M., & Castaño, D. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02058 · Cited by 54

Tissue-specific expression of IgG receptors by human macrophages ex vivo

Bruggeman, C. W., Houtzager, J., Dierdorp, B., Kers, J., Pals, S. T., Lutter, R., van Gulik, T. M., den Haan, J. M. M., van den Berg, T. K., van Bruggen, R., et al. (2019) · PLoS ONE · doi:10.1371/journal.pone.0223264 · Cited by 56

The role of macrophages in protective and pathological responses to Toxoplasma gondii

Park, J., & Hunter, C. A. (2020) · Parasite Immunology · doi:10.1111/pim.12712 · Cited by 54

A molecular atlas of innate immunity to adjuvanted and live attenuated vaccines, in mice

Lee, A. W. Q., Scott, M. K. D., Wimmers, F., Arunachalam, P. S., Luo, W., Fox, C. B., Tomai, M. A., Khatri, P., & Pulendran, B. (2022) · Nature Communications · doi:10.1038/s41467-022-28197-9 · Cited by 52

Rheumatoid arthritis and osteoimmunology: The adverse impact of a deregulated immune system on bone metabolism

Andreev, D., Kachler, K., Schett, G. A., & Bözec, A. (2022) · Bone · doi:10.1016/j.bone.2022.116468 · Cited by 57

Poxviruses and the immune system: Implications for monkeypox virus

Saghazadeh, A., & Rezaei, N. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.109364 · Cited by 52

The acute inflammatory response of teleost fish

Soliman, A. M., & Barreda, D. R. (2023) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2023.104731 · Cited by 56

Optineurin deficiency contributes to impaired cytokine secretion and neutrophil recruitment in bacteria driven colitis

Chew, T. S., O’Shea, N. R., Sewell, G. W., Oehlers, S. H., Mulvey, C. M., Crosier, P. S., Godovac‐Zimmermann, J., Bloom, S. L., Smith, A. M., & Segal, A. W. (2015) · Disease Models & Mechanisms · doi:10.1242/dmm.020362 · Cited by 54

Moderate-intensity exercise alters markers of alternative activation in circulating monocytes in females: a putative role for PPARγ

Ruffino, J. S., Davies, N. A., Morris, K., Ludgate, M., Zhang, L., Webb, R., & Thomas, A. W. (2016) · European Journal of Applied Physiology · doi:10.1007/s00421-016-3414-y · Cited by 56

From macrophage to osteoclast – How metabolism determines function and activity

Kubatzky, K. F., Uhle, F., & Eigenbrod, T. (2018) · Cytokine · doi:10.1016/j.cyto.2018.06.013 · Cited by 52

Maternal-Fetal Interplay in Zika Virus Infection and Adverse Perinatal Outcomes

Teixeira, F. M. E., Pietrobon, A. J., Oliveira, L. D. M., Oliveira, L. M. D. S., & Sato, M. N. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00175 · Cited by 56

Links between Immune Cells from the Periphery and the Brain in the Pathogenesis of Epilepsy: A Narrative Review

Yamanaka, G., Morıchı, S., Takamatsu, T., Watanabe, Y., Suzuki, S., Ishida, Y., Oana, S., Yamazaki, T., Takata, F., & Kawashima, H. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22094395 · Cited by 54

TLR7 and TLR9 ligands regulate antigen presentation by macrophages

Celhar, T., Pereira-Lopes, S., Thornhill, S. I., Lee, H. Y., Dhillon, M. K., Poidinger, M., Connolly, J. E., Lim, L. H. K., Biswas, S. K., & Fairhurst, A.-M. (2016) · International Immunology · doi:10.1093/intimm/dxv066 · Cited by 52

MCP1 triggers monocyte dysfunctions during abnormal osteogenic differentiation of mesenchymal stem cells in ankylosing spondylitis

Xie, Z., Wang, P., Li, J., Li, Y., Wang, S., Wu, X., Sun, S., Cen, S., Su, H., Deng, W., et al. (2016) · Journal of Molecular Medicine · doi:10.1007/s00109-016-1489-x · Cited by 53

Anti-TLR7 Antibody Protects Against Lupus Nephritis in NZBWF1 Mice by Targeting B Cells and Patrolling Monocytes

Murakami, Y., Fukui, R., Tanaka, R., Motoi, Y., Kanno, A., Sato, R., Yamaguchi, K., Amano, H., Furukawa, Y., Suzuki, H., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.777197 · Cited by 56

The role of monocytes in thrombotic diseases: a review

Han, Z., Liu, Q., Li, H., Zhang, M., You, L., Lin, Y., Wang, K., Gou, Q., Wang, Z., Zhou, S., et al. (2023) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2023.1113827 · Cited by 52

Exposure to a Social Stressor Induces Translocation of Commensal Lactobacilli to the Spleen and Priming of the Innate Immune System

Lafuse, W. P., Gearinger, R. L., Fisher, S., Nealer, C., Mackos, A. R., & Bailey, M. T. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601269 · Cited by 51

mTOR masters monocyte development in bone marrow by decreasing the inhibition of STAT5 on IRF8

Zhao, Y., Shen, X., Na, N., Chu, Z., Su, H., Chao, S., Shi, L., Xu, Y., Zhang, L., Shi, B., et al. (2018) · Blood · doi:10.1182/blood-2017-04-777128 · Cited by 51

Resident cardiac macrophages: crucial modulators of cardiac (patho)physiology

Sansonetti, M., Waleczek, F. J. G., Jung, M., Thum, T., & Perbellini, F. (2020) · Basic Research in Cardiology · doi:10.1007/s00395-020-00836-6 · Cited by 53

The molecular mechanism of LRP1 in physiological vascular homeostasis and signal transduction pathways

He, Z., Wang, G., Wu, J., Tang, Z., & Luo, M. (2021) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2021.111667 · Cited by 50

Diverging biological roles among human monocyte subsets in the context of tuberculosis infection

Balboa, L., Barrios‐Payán, J., González‐Domínguez, E., Lastrucci, C., Lugo‐Villarino, G., Mata‐Espinosa, D., Schierloh, P., Kviatcovsky, D., Neyrolles, O., Maridonneau‐Parini, I., et al. (2015) · Clinical Science · doi:10.1042/cs20150021 · Cited by 51

A miR-150/TET3 pathway regulates the generation of mouse and human non-classical monocyte subset

Selimoglu‐Buet, D., Rivière, J., Ghamlouch, H., Bencheikh, L., Lacout, C., Morabito, M., Diop, M. K., Meurice, G., Breckler, M., Chauveau, A., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-07801-x · Cited by 55

The expanding landscape of inflammatory cells affecting cancer therapy

Weissleder, R., & Pittet, M. J. (2020) · Nature Biomedical Engineering · doi:10.1038/s41551-020-0524-y · Cited by 51

Androgens predispose males to monocyte-mediated immunopathology by inducing the expression of leukocyte recruitment factor CXCL1

Sellau, J., Groneberg, M., Fehling, H., Thye, T., Hoenow, S., Marggraff, C., Weskamm, L. M., Hansen, C. S., Stanelle‐Bertram, S., Kuehl, S., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-17260-y · Cited by 51

Contributions of monocytes to nervous system disorders

Garré, J. M., & Yang, G. (2018) · Journal of Molecular Medicine · doi:10.1007/s00109-018-1672-3 · Cited by 53

The Changes of Leukocytes in Brain and Blood After Intracerebral Hemorrhage

Mei, S., Shao, Y., Fang, Y., Lü, J., Zheng, J., Xu, S., Wu, H., Sun, Z., Yu, J., Chen, S., et al. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.617163 · Cited by 51

Neuron-macrophage crosstalk in the intestine: a “microglia” perspective

Verheijden, S., Schepper, S. D., & Boeckxstaens, G. E. (2015) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2015.00403 · Cited by 54

Epigenetic regulation of neutrophil development and function

Ostuni, R., Natoli, G., Cassatella, M. A., & Tamassia, N. (2016) · Seminars in Immunology · doi:10.1016/j.smim.2016.04.002 · Cited by 51

The Therapeutic Potential of Monocyte/Macrophage Manipulation in the Treatment of Chemotherapy-Induced Painful Neuropathy

Montague-Cardoso, K., & Malcangio, M. (2017) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2017.00397 · Cited by 54

CX3CR1 differentiates F4/80low monocytes into pro-inflammatory F4/80high macrophages in the liver

Lee, Y., Kim, M. H., Yi, H., Kim, S. Y., Kim, H., Kim, J. H., Yeon, J. E., Byun, K. S., Byun, J.-S., & Jeong, W. (2018) · Scientific Reports · doi:10.1038/s41598-018-33440-9 · Cited by 52

Therapeutic Modulation of Autophagy in Leukaemia and Lymphoma

Djavaheri‐Mergny, M., Giuriato, S., Tschan, M. P., & Humbert, M. (2019) · Cells · doi:10.3390/cells8020103 · Cited by 52

Presence and activation of pro-inflammatory macrophages are associated with CRYAB expression in vitro and after peripheral nerve injury

Lim, E.-M. F., Hoghooghi, V., Hagen, K. M., Kapoor, K., Frederick, A., Finlay, T. M., & Ousman, S. S. (2021) · Journal of Neuroinflammation · doi:10.1186/s12974-021-02108-z · Cited by 53

Generation and Functional Characterization of Monocytes and Macrophages Derived from Human Induced Pluripotent Stem Cells

Cao, X., van den Hil, F. E., Mummery, C. L., & Orlova, V. V. (2020) · Current Protocols in Stem Cell Biology · doi:10.1002/cpsc.108 · Cited by 52

Triptolide induces PANoptosis in macrophages and causes organ injury in mice

Zhang, H., Li, Y., Shi, Z., Liang, Q.-Q., Chen, S., You, Y.-P., Tao, Y., Xu, R., Xu, L., Ouyang, D., et al. (2023) · APOPTOSIS · doi:10.1007/s10495-023-01886-6 · Cited by 50

Targeting Macrophage Phenotypes and Metabolism as Novel Therapeutic Approaches in Atherosclerosis and Related Cardiovascular Diseases

Wang, J., Wu, Q., Wang, X., Liu, H., Chen, M., Xu, L. N., Zhang, Z., Li, K., Li, W., & Zhong, J. (2024) · Current Atherosclerosis Reports · doi:10.1007/s11883-024-01229-z · Cited by 55

Macrophages and Gut Barrier Function: Guardians of Gastrointestinal Health in Post-Inflammatory and Post-Infection Responses

Meng, E. X., Verne, G. N., & Zhou, Q. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25179422 · Cited by 56

Control of macrophage 3D migration: a therapeutic challenge to limit tissue infiltration

Maridonneau‐Parini, I. (2014) · Immunological Reviews · doi:10.1111/imr.12214 · Cited by 51

Whole Genome Analysis of Lactobacillus plantarum Strains Isolated From Kimchi and Determination of Probiotic Properties to Treat Mucosal Infections by Candida albicans and Gardnerella vaginalis

Beck, B. R., Park, G.-S., Lee, Y. H., Im, S., Jeong, D. Y., & Kang, J. (2019) · Frontiers in Microbiology · doi:10.3389/fmicb.2019.00433 · Cited by 52

Pharmacological validation of targets regulating CD14 during macrophage differentiation

Jimenez‐Duran, G., Luque-Martin, R., Patel, M. N., Koppe, E. L., Bernard, S. G., Sharp, C. H., Buchan, N. S., Rea, C., de Winther, M. P. J., Turan, N., et al. (2020) · EBioMedicine · doi:10.1016/j.ebiom.2020.103039 · Cited by 49

RISING STARS: androgens and immune cell function

Ainslie, R. J., Simitsidellis, I., Kirkwood, P. M., & Gibson, D. A. (2024) · Journal of Endocrinology · doi:10.1530/joe-23-0398 · Cited by 48

MAIT Cells in Barrier Tissues: Lessons from Immediate Neighbors

Amini, A., Pang, D., Hackstein, C.-P., & Klenerman, P. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.584521 · Cited by 49

Macrophage-mediated extracellular matrix remodeling controls host Staphylococcus aureus susceptibility in the skin

Voisin, B., Nadella, V., Doebel, T., Goel, S., Sakamoto, K., Ayush, O., Jo, J., Kelly, M. C., Kobayashi, T., Jiang, J. X., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.06.006 · Cited by 50

Recruited monocytes modulate malaria-induced lung injury through CD36-mediated clearance of sequestered infected erythrocytes

Lagassé, H. A. D., Anidi, I. U., Craig, J. M., Limjunyawong, N., Poupore, A. K., Mitzner, W., & Scott, A. L. (2015) · Journal of Leukocyte Biology · doi:10.1189/jlb.4hi0315-130rrr · Cited by 51

Killing Is Not Enough: How Apoptosis Hijacks Tumor-Associated Macrophages to Promote Cancer Progression

Weigert, A., Mora, J., Sekar, D., Syed, S. N., & Brüne, B. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-39406-0_9 · Cited by 48

Development and Functional Differentiation of Tissue-Resident Versus Monocyte-Derived Macrophages in Inflammatory Reactions

Italiani, P., & Boraschi, D. (2017) · Results and problems in cell differentiation · doi:10.1007/978-3-319-54090-0_2 · Cited by 53

Pre/pro-B cells generate macrophage populations during homeostasis and inflammation

Audzevich, T., Bashford-Rogers, R. J. M., Mabbott, N. A., Frampton, D., Freeman, T. C., Potocnik, A. J., Kellam, P., & Gilroy, D. W. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1616417114 · Cited by 48

Current advances in the nano-delivery of celastrol for treating inflammation-associated diseases

Fang, G., & Tang, B. (2020) · Journal of Materials Chemistry B · doi:10.1039/d0tb01939a · Cited by 48

Neuroimmune Responses Mediate Depression-Related Behaviors following Acute Colitis

Gadotti, V. M., Andonegui, G., Zhang, Z., M’Dahoma, S., Baggio, C. H., Chen, L., Basso, L., Altier, C., MacNaughton, W. K., Kubes, P., et al. (2019) · iScience · doi:10.1016/j.isci.2019.05.012 · Cited by 47

A single-cell lung atlas of complement genes identifies the mesothelium and epithelium as prominent sources of extrahepatic complement proteins

Chaudhary, N., Jayaraman, A., Reinhardt, C., Campbell, J. D., & Bosmann, M. (2022) · Mucosal Immunology · doi:10.1038/s41385-022-00534-7 · Cited by 47

Unraveling the potential of 3D bioprinted immunomodulatory materials for regulating macrophage polarization: State-of-the-art in bone and associated tissue regeneration

Dutta, S. D., Patil, T. V., Ganguly, K., Randhawa, A., & Lim, K. (2023) · Bioactive Materials · doi:10.1016/j.bioactmat.2023.05.014 · Cited by 52

Coupling between macrophage phenotype, angiogenesis and bone formation by calcium phosphates

Duan, R., Zhang, Y., van Dijk, L., Barbieri, D., van den Beucken, J. J. J. P., Yuan, H., & de Bruijn, J. D. (2021) · Materials Science and Engineering C · doi:10.1016/j.msec.2021.111948 · Cited by 47

Role of Monocyte-Derived MicroRNA106b∼25 in Resilience to Social Stress

Pfau, M. L., Menard, C., Cathomas, F., Desland, F., Kana, V., Chan, K. L., Shimo, Y., LeClair, K., Flanigan, M. E., Aleyasin, H., et al. (2019) · Biological Psychiatry · doi:10.1016/j.biopsych.2019.02.023 · Cited by 46

Too sweet to resist: Control of immune cell function by O-GlcNAcylation

de Jesus, T., Shukla, S., & Ramakrishnan, P. (2018) · Cellular Immunology · doi:10.1016/j.cellimm.2018.05.010 · Cited by 51

The Immunomechanical Checkpoint PYK2 Governs Monocyte-to-Macrophage Differentiation in Pancreatic Cancer

Xie, W., Yu, X., Yang, Q., Ke, N., Wang, P., Kong, H., Wu, X., Ma, P., Chen, L., Yang, J., et al. (2025) · Cancer Discovery · doi:10.1158/2159-8290.cd-24-1712 · Cited by 49

IL‐3 synergises with basophil‐derived IL‐4 and IL‐13 to promote the alternative activation of human monocytes

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The Atypical Inhibitor of NF-κB, IκBζ, Controls Macrophage Interleukin-10 Expression

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