Constant replenishment from circulating monocytes maintains the macrophage pool in the intestine of adult mice

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

CCL2 recruits inflammatory monocytes to facilitate breast-tumour metastasis

Qian, B.-Z., Li, J., Zhang, H., Kitamura, T., Zhang, J., Campion, L. R., Kaiser, E. A., Snyder, L. A., & Pollard, J. W. (2011) · Nature · doi:10.1038/nature10138 · Cited by 2,874

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

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

Tissue-resident macrophages

Davies, L. C., Jenkins, S. J., Allen, J. E., & Taylor, P. R. (2013) · Nature Immunology · doi:10.1038/ni.2705 · Cited by 2,096

Monocyte emigration from bone marrow during bacterial infection requires signals mediated by chemokine receptor CCR2

Serbina, N. V., & Pamer, E. G. (2006) · Nature Immunology · doi:10.1038/ni1309 · Cited by 1,658

Local self-renewal can sustain CNS microglia maintenance and function throughout adult life

Ajami, B., Bennett, J. L., Krieger, C., Tetzlaff, W., & Rossi, F. M. V. (2007) · Nature Neuroscience · doi:10.1038/nn2014 · Cited by 1,643

Origin and functions of tissue macrophages

Epelman, S., Lavine, K. J., & Randolph, G. J. (2014) · Immunity · doi:10.1016/j.immuni.2014.06.013 · Cited by 1,585

Embryonic and Adult-Derived Resident Cardiac Macrophages Are Maintained through Distinct Mechanisms at Steady State and during Inflammation

Epelman, S., Lavine, K. J., Beaudin, A. E., Sojka, D. K., Carrero, J. A., Calderon, B., Brija, T., Gautier, E. L., Ivanov, S., Satpathy, A. T., et al. (2014) · Immunity · doi:10.1016/j.immuni.2013.11.019 · Cited by 1,494

Role of innate immunity and myeloid cells in susceptibility to allergic disease

Noel, J. C., & Berin, M. C. (2021) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.14654 · Cited by 15

Disruption of monocyte-macrophage differentiation and trafficking by a heme analog during active inflammation

Schaefer, R. E. M., Callahan, R. C., Atif, S. M., Orlicky, D. J., Cartwright, I. M., Fontenot, A. P., Colgan, S. P., & Onyiah, J. C. (2021) · Mucosal Immunology · doi:10.1038/s41385-021-00474-8 · Cited by 14

Lactobacillus brevis KB290 With Vitamin A Ameliorates Murine Intestinal Inflammation Associated With the Increase of CD11c+ Macrophage/CD103− Dendritic Cell Ratio

Fuke, N., Takagi, T., Higashimura, Y., Tsuji, T., Umeda, R., Mizushima, K., Tanaka, M., Suganuma, H., Aizawa, K., Yajima, N., et al. (2018) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izx003 · Cited by 15

The stromal vascular fraction mitigates radiation-induced gastrointestinal syndrome in mice

Bensemmane, L., Squiban, C., Demarquay, C., Mathieu, N., Benderitter, M., Guen, B. L., Milliat, F., & Linard, C. (2021) · Stem Cell Research & Therapy · doi:10.1186/s13287-021-02373-y · Cited by 16

Single‐Cell Insights Into Macrophage Subtypes in Pulmonary Infections

Lin, Z., Zheng, Y., Zhong, Y., & Wang, H. (2026) · Advanced Science · doi:10.1002/advs.202510758 · Cited by 13

Chronic stress, gut microbiota, and immunity: interconnections and implications for health

Jia, H., Guo, X., Wei, Y., Can, C., He, N., Zhang, H., Yang, X., Wu, H., Liu, W., & Ma, D. (2025) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-025-05376-y · Cited by 14

A Fiber-Rich Diet and Radiation-Induced Injury in the Murine Intestinal Mucosa

Malipatlolla, D. K., Devarakonda, S., Patel, P., Sjöberg, F., Rascón, A., Grandér, R., Skokic, V., Kalm, M., Danial, J., Mehdin, E., et al. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms23010439 · Cited by 13

Diet-induced obesity alters intestinal monocyte-derived and tissue-resident macrophages and increases intestinal permeability in female mice independent of tumor necrosis factor

Breznik, J. A., Jury, J., Verdu, E. F., Sloboda, D. M., & Bowdish, D. M. E. (2023) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00231.2022 · Cited by 12

Metabolic and functional remodeling of colonic macrophages in response to high-fat diet-induced obesity

Castoldi, Â., Sanin, D. E., Bakker, N. V. T., de Aguiar, C. F., Monteiro, L. D. B., Rana, N., Grzes, K. M., Kabat, A. M., Curtis, J., Cameron, A. M., et al. (2023) · iScience · doi:10.1016/j.isci.2023.107719 · Cited by 14

Vitisin A, as a Type of Pyranoanthocyanin, Suppresses Inflammation by Restricting Hematopoietic Stem Cell Differentiation toward Monocytes in Bone Marrow

Li, X., Li, Z., Cai, D., Li, Y., Zhu, Y., Jiao, R., Lai, C., Sun, J., & Bai, W. (2023) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.3c03119 · Cited by 13

Co-inhibition of TGF-β and PD-L1 pathways in a metastatic colorectal cancer mouse model triggers interferon responses, innate cells and T cells, alongside metabolic changes and tumor resistance

Nair, R., Lannagan, T. R. M., Jackstadt, R., Andrusaite, A. T., Cole, J. J., Boyne, C., Nibbs, R. J. B., Sansom, O. J., & Milling, S. W. F. (2024) · OncoImmunology · doi:10.1080/2162402x.2024.2330194 · Cited by 13

Early Antiretroviral Therapy Prevents Viral Infection of Monocytes and Inflammation in Simian Immunodeficiency Virus-Infected Rhesus Macaques

Rabezanahary, H., Clain, J. A., Racine, G., Andreani, G., Benmadid-Laktout, G., Borde, C., Mammano, F., Mésplède, T., Ancuța, P., Zghidi‐Abouzid, O., et al. (2020) · Journal of Virology · doi:10.1128/jvi.01478-20 · Cited by 13

Epigenetics and tissue immunity—Translating environmental cues into functional adaptations*

Tuong, Z. K., Stewart, B. J., Guo, S. A., & Clatworthy, M. R. (2021) · Immunological Reviews · doi:10.1111/imr.13036 · Cited by 13

The origins of resident macrophages in mammary gland influence the tumorigenesis of breast cancer

Yang, Y., Hou, J., Liu, J., Bhushan, S., & Wu, G. (2022) · International Immunopharmacology · doi:10.1016/j.intimp.2022.109047 · Cited by 14

Isolation and functional characterisation of lamina propria leukocytes from helminth-infected, murine small intestine

Webster, H. C., Andrusaite, A. T., Shergold, A. L., Milling, S. W. F., & Perona‐Wright, G. (2019) · Journal of Immunological Methods · doi:10.1016/j.jim.2019.112702 · Cited by 14

Intestinal Mononuclear Phagocytes in Health and Disease

Sanders, T. J., Yrlid, U., & Maloy, K. J. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0047-2016 · Cited by 13

Relationship between Immunological Abnormalities in Rat Models of Diabetes Mellitus and the Amplification Circuits for Diabetes

Takeda, Y., Shimomura, T., Asao, H., & Wakabayashi, I. (2017) · Journal of Diabetes Research · doi:10.1155/2017/4275851 · Cited by 13

Srsf3-Dependent APA Drives Macrophage Maturation and Limits Atherosclerosis

Yang, X., Zhang, X., Tian, Y., Yang, J., Jia, Y., Xie, Y., Cheng, L., Chen, S., Wu, L., Qin, Y., et al. (2025) · Circulation Research · doi:10.1161/circresaha.124.326111 · Cited by 13

Necrotizing Enterocolitis: A Comprehensive Review on Toll-like Receptor 4-Mediated Pathophysiology, Clinical, and Therapeutic Insights

Ishiyama, A., Jang, H., Dintaman, J. M., Duess, J. W., Tragesser, C. J., & Sodhi, C. P. (2025) · Biomedicines · doi:10.3390/biomedicines13092288 · Cited by 17

Interleukin-4 protects mice against lethal influenza and Streptococcus pneumoniae co-infected pneumonia

Yang, P., Wang, X., Wang, H., Xu, W., Wu, K., Go, X., Yin, Y., & Zhang, X. (2021) · Clinical & Experimental Immunology · doi:10.1111/cei.13628 · Cited by 11

PCBP1 acts as a regulator of CCL2 expression in macrophages to induce recruitment of monocyte-derived macrophages into the inflamed colon

Yang, X., Yabe‐Wada, T., Han, J., Saito, F., Ogasawara, C., Yamada, S., & Onai, N. (2023) · International Immunology · doi:10.1093/intimm/dxad003 · Cited by 12

The multivalency game ruling the biology of immunity

Aiassa, L. V., Battaglia, G., & Rizzello, L. (2023) · Biophysics Reviews · doi:10.1063/5.0166165 · Cited by 11

Natural product/diet-based regulation of macrophage polarization: Implications in treatment of inflammatory-related diseases and cancer

Ashrafizadeh, M., Aref, A. R., Sethi, G., Ertaş, Y. N., & Wang, L. (2024) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2024.109647 · Cited by 13

The longitudinal characterization of immune responses in COVID-19 patients reveals novel prognostic signatures for disease severity, patients’ survival and long COVID

Noviello, M., LORENZO, R. D., Chimienti, R., Maugeri, N., de Lalla, C., Siracusano, G., Lorè, N. I., Rancoita, P. M. V., Cugnata, F., Tassi, E., et al. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1381091 · Cited by 13

Reactive oxygen species regulate early development of the intestinal macrophage-microbiome interface

Moghadam, Z. M., Zhao, B., Raynaud, C., Strohmeier, V., Neuber, J., Lößlein, A. K., Qureshi, S., Gres, V., Ziegelbauer, T., Baasch, S., et al. (2025) · Blood · doi:10.1182/blood.2024025240 · Cited by 13

NAD+ modulation of intestinal macrophages renders anti-inflammatory functionality and ameliorates gut inflammation

Kim, Y., Ko, I., Yi, E.-J., Kim, J., Hong, Y. R., Lee, W., & Chang, S.-Y. (2025) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2025.117938 · Cited by 12

Quantitative In-Depth Transcriptome Analysis Implicates Peritoneal Macrophages as Important Players in the Complement and Coagulation Systems

Paivandy, A., Akula, S., Lara, S., Fu, Z., Olsson, A., Kleinau, S., Pejler, G., & Hellman, L. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23031185 · Cited by 12

Anti‐β7 integrin treatment impedes the recruitment on non‐classical monocytes to the gut and delays macrophage‐mediated intestinal wound healing

Sommer, K., Heidbreder, K., Kreiss, L. A., Dedden, M., Paap, E., Wiendl, M., Becker, E. M., Atreya, R. N., Müller, T. M., Atreya, I., et al. (2023) · Clinical and Translational Medicine · doi:10.1002/ctm2.1233 · Cited by 11

Functional specialization of short-lived and long-lived macrophage subsets in human tonsils

Alaoui, L., Villar, J., Leclère, R., Gallou, S. L., Relouzat, F., Michaud, H., Tarte, K., Teissier, N., Favier, B., Roussel, M., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20230002 · Cited by 11

Tumor-associated macrophages, multi-tasking cells in the cancer landscape

Marelli, G., Allavena, P., & Erreni, M. (2015) · Cancer Research Frontiers · doi:10.17980/2015.149 · Cited by 13

CD103+CD11b− salivary gland dendritic cells have antigen cross‐presenting capacity

Lu, L., Tanaka, Y., Ishii, N., Sasano, T., & Sugawara, S. (2016) · European Journal of Immunology · doi:10.1002/eji.201646631 · Cited by 12

Maturation Phenotype of Peripheral Blood Monocyte/Macrophage After Stimulation with Lipopolysaccharides in Irritable Bowel Syndrome

Rodríguez, Ó., Hernández-Ruiz, J., López‐Vidal, Y., Charúa-Guindic, L., Escobedo, G., & Schmulson, M. J. (2017) · Journal of Neurogastroenterology and Motility · doi:10.5056/jnm16137 · Cited by 12

Isolation and Identification of Murine Serous Cavity Macrophages

Bain, C. C., & Jenkins, S. J. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-7837-3_5 · Cited by 12

Control of myeloid cell density in barrier tissues

Lohrmann, F., Forde, A. J., Merck, P., & Henneke, P. (2020) · FEBS Journal · doi:10.1111/febs.15436 · Cited by 11

Trichuris muris infection drives cell-intrinsic IL4R alpha independent colonic RELMα+ macrophages

Forman, R. A., Logunova, L., Smith, H., Wemyss, K., Mair, I., Boon, L., Allen, J. E., Müller, W., Pennock, J. L., & Else, K. J. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009768 · Cited by 12

Metabolic adaption of mucosal macrophages: Is metabolism a driver of persistence across tissues?

Bennett, C. L., & Perona‐Wright, G. (2023) · Mucosal Immunology · doi:10.1016/j.mucimm.2023.06.006 · Cited by 11

M1 and M2 Macrophages Differentially Regulate Colonic Crypt Renewal

Raveenthiraraj, S., Awanis, G., Chieppa, M., O’Connell, A. E., & Sobolewski, A. (2023) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izad270 · Cited by 11

Landscape of Interactions between Stromal and Myeloid Cells in Ileal Crohn’s Disease; Indications of an Important Role for Fibroblast-Derived CCL-2

Dovrolis, N., Valatas, V., Drygiannakis, I., Filidou, E., Spathakis, M., Kandilogiannakis, L., Tarapatzi, G., Arvanitidis, K. I., Bamias, G., Vradelis, S., et al. (2024) · Biomedicines · doi:10.3390/biomedicines12081674 · Cited by 11

Role of macrophages in vascular calcification: From the perspective of homeostasis

Dong, R., Ji, Z., Wang, M., & Ma, G. (2024) · International Immunopharmacology · doi:10.1016/j.intimp.2024.113635 · Cited by 11

Non-classical monocytes and its potential in diagnosing sepsis post cardiac surgery

Sebastian, A., Sanju, S., Jain, P., Priya, V. V., Varma, P. K., & Mony, U. (2021) · International Immunopharmacology · doi:10.1016/j.intimp.2021.108037 · Cited by 11

The Impact of Phase-Specific Macrophage Depletion on Intestinal Anastomotic Healing

Winter, M., Heitplatz, B., Koppers, N., Mohr, A., Bungert, A. D., Juratli, M. A., Struecker, B., Varga, G., Pascher, A., & Becker, F. (2023) · Cells · doi:10.3390/cells12071039 · Cited by 12

Reduction of absolute monocyte counts is associated with the severity of preterm necrotizing enterocolitis

Wang, Z., Chong, Q., Zhou, J., Gao, T., Zhu, K., Gong, X., Sheng, Q., & Lv, Z. (2023) · Jornal de Pediatria · doi:10.1016/j.jped.2023.02.006 · Cited by 11

Fate-Mapping Macrophages: From Ontogeny to Functions

Ahlback, A., & Gentek, R. (2023) · Methods in molecular biology · doi:10.1007/978-1-0716-3437-0_2 · Cited by 13

Single cell atlas of human gastric muscle immune cells and macrophage-driven changes in idiopathic gastroparesis

Chikkamenahalli, L. L., Jessen, E., Bernard, C. E., Ip, W., Breen‐Lyles, M. K., Cipriani, G., Pullapantula, S. R., Li, Y., AlAsfoor, S., Wilson, L., et al. (2024) · iScience · doi:10.1016/j.isci.2024.108991 · Cited by 12

Extraembryonic hematopoietic lineages—to macrophages and beyond

Sommer, A., & Perdiguero, E. G. (2024) · Experimental Hematology · doi:10.1016/j.exphem.2024.104285 · Cited by 12

Microbial Colonization in Adulthood Shapes the Intestinal Macrophage Compartment

Schmidt, F., Dahlke, K., Batra, A., Keye, J., Wu, H., Friedrich, M., Glauben, R., Ring, C., Loh, G., Schaubeck, M., et al. (2019) · Journal of Crohn s and Colitis · doi:10.1093/ecco-jcc/jjz036 · Cited by 12

Saccharomyces boulardii Strain CNCM I-745 Modifies the Mononuclear Phagocytes Response in the Small Intestine of Mice Following Salmonella Typhimurium Infection

Ibáñez, L., Pontier-Bres, R., Larbret, F., Rekima, A., Verhasselt, V., Blin‐Wakkach, C., & Czerucka, D. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.00643 · Cited by 11

A two‐step human culture system replicates intestinal monocyte maturation cascade: Conversion of tissue‐like inflammatory monocytes into macrophages

Bsat, M., Chapuy, L., Rubio, M., & Sarfati, M. (2020) · European Journal of Immunology · doi:10.1002/eji.202048555 · Cited by 11

Pharmaceutical grade synthetic peptide Thr-Glu-Lys-Lys-Arg-Arg-Glu-Thr-Val-Glu-Arg-Glu-Lys-Glu ameliorates DSS-induced murine colitis by reducing the number and pro-inflammatory activity of colon tissue-infiltrating Ly6G+ granulocytes and Ly6C+ monocytes

Chulkina, M., Av, P., & Ataullakhanov, R. I. (2020) · Peptides · doi:10.1016/j.peptides.2020.170364 · Cited by 11

Selective induction of anti-inflammatory monocyte-platelet aggregates in a model of pulsatile blood flow at low shear rates

Takeda, Y., Marumo, M., Nara, H., Feng, Z.-G., Asao, H., & Wakabayashi, I. (2016) · Platelets · doi:10.3109/09537104.2016.1153616 · Cited by 11

Editorial

Murray, P. J. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2015.11.004 · Cited by 11

Early ART reduces viral seeding and innate immunity in liver and lungs of SIV-infected macaques

Clain, J. A., Rabezanahary, H., Racine, G., Boutrais, S., Soundaramourty, C., Beauparlant, C. J., Jenabian, M.-A., Droit, A., Ancuța, P., Zghidi‐Abouzid, O., et al. (2023) · JCI Insight · doi:10.1172/jci.insight.167856 · Cited by 11

Early precursor-derived pituitary gland tissue-resident macrophages play a pivotal role in modulating hormonal balance

Lehtonen, H., Jokela, H., Hofmann, J. I., Tola, L., Mehmood, A., Ginhoux, F., Becher, B., Greter, M., Yegutkin, G. G., Salmi, M., et al. (2025) · Cell Reports · doi:10.1016/j.celrep.2024.115227 · Cited by 9

Novel insights into embryonic cardiac macrophages

Gula, G., & Ratajska, A. (2022) · Developmental Biology · doi:10.1016/j.ydbio.2022.05.003 · Cited by 12

Turnover Kinetics of Pancreatic Macrophages in Lean and Obese Diabetic Mice

Ma, Z., & Ruedl, C. (2022) · Frontiers in Endocrinology · doi:10.3389/fendo.2022.858422 · Cited by 10

NOD2 in monocytes negatively regulates macrophage development through TNFalpha

Chauvin, C., Álvarez-Simón, D., Radulovic, K., Boulard, O., Laine, W., Delacre, M., Waldschmitt, N., Segura, É., Kluza, J., Chamaillard, M., et al. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1181823 · Cited by 10

A small sustained increase in NOD1 abundance promotes ligand-independent inflammatory and oncogene transcriptional responses

Rommereim, L. M., Akhade, A. S., Dutta, B., Hutcheon, C. J., Lounsbury, N., Rostomily, C., Savan, R., Fraser, I. D. C., Germain, R. N., & Subramanian, N. (2020) · Science Signaling · doi:10.1126/scisignal.aba3244 · Cited by 10

Response to Oxidative Burst-Induced Hypoxia Is Associated With Macrophage Inflammatory Profiles as Revealed by Cellular Genome-Wide Association

Emam, M., Tabatabaei, S., Sargolzaei, M., & Mallard, B. A. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.688503 · Cited by 10

Analysis and Purification of Mouse Intestinal Dendritic Cell and Macrophage Subsets by Flow Cytometry

Koscsó, B., & Bogunovic, M. (2016) · Current Protocols in Immunology · doi:10.1002/cpim.11 · Cited by 10

Interactions of helminths with macrophages: therapeutic potential for inflammatory intestinal disease

Smith, H., Forman, R. A., Mair, I., & Else, K. J. (2018) · Expert Review of Gastroenterology & Hepatology · doi:10.1080/17474124.2018.1505498 · Cited by 11

Regional Control of Regulatory Immune Cells in the Intestine

Morhardt, T. L., Hayashi, A., Kao, J. Y., & Kamada, N. (2018) · Current Pathobiology Reports · doi:10.1007/s40139-018-0156-z · Cited by 10

High-dimensional profiling demonstrates complexity, tissue imprinting, and lineage-specific precursors within the mononuclear phagocyte compartment of the human intestinePreprint

Fenton, T. M., Wulff, L., Jones, G., Vandamme, J., Jørgensen, P. B., Bain, C. C., Lee, J., Izarzugaza, J. M. G., Belling, K., Ho, G., et al. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.03.28.437379 · Cited by 10

Pancreas Resident Macrophage-Induced Fibrosis Has Divergent Roles in Pancreas Inflammatory Injury and PDACPreprint

Baer, J. M., Zuo, C., Kang, L., de la Lastra, A. A., Borcherding, N. C., Knolhoff, B. L., Bogner, S. J., Zhu, Y., Lewis, M. A., Zhang, N., et al. (2022) · SSRN Electronic Journal · doi:10.1101/2022.02.09.479745 · Cited by 10

Comparison of iron-reduced and iron-supplemented semisynthetic diets in T cell transfer colitis

Markota, A., Metzger, R., Heiseke, A. F., Jandl, L., Dursun, E., Eisenächer, K., Reindl, W., Haller, D., & Krug, A. B. (2019) · PLoS ONE · doi:10.1371/journal.pone.0218332 · Cited by 9

Neuroimmune Crossroads: The Interplay of the Enteric Nervous System and Intestinal Macrophages in Gut Homeostasis and Disease

Lou, M., Heuckeroth, R. O., & Tjaden, N. E. B. (2024) · Biomolecules · doi:10.3390/biom14091103 · Cited by 11

The role of enteric nervous system and GDNF in depression: Conversation between the brain and the gut

Liang, C., Wei, S., Ji, Y., Lin, J., Jiao, W., Li, Z., Yan, F., & Xi, J. (2024) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2024.105931 · Cited by 13

Multi-omics analysis identified macrophages as key contributors to sex-related differences in ulcerative colitis

Fang, X., Yang, J., Liu, Y., Lin, Y., Li, Y., Yin, X., Dou, X., & Miao, C. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1569271 · Cited by 9

Macrophage metabolism in inflammatory heart disease: new insights and therapeutic implications

Xiang, A., Chang, A., Zhou, J., Jin, J., Zhang, X., & Wang, Q. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1664538 · Cited by 11

Restored clearance of senescent neutrophils by tissue-resident macrophages limits organ aging

Tan, Y. J., Conley, T. E., Yao, F., Garcia-Marques, F. J., Akinyemi, D. E., Dinh, V. V., Wang, Q., Bermudez, A., Kim, J., Belk, J. A., et al. (2026) · Science · doi:10.1126/science.aea3075 · Cited by 10

Mucus blocks probiotics but increases penetration of motile pathogens and induces TNF‐α and IL‐8 secretion

Sharma, A., Raman, V., Lee, J., & Forbes, N. S. (2020) · Biotechnology and Bioengineering · doi:10.1002/bit.27383 · Cited by 9

Cultures of Human Skin Mast Cells, an Attractive In Vitro Model for Studies of Human Mast Cell Biology

Akula, S., Tripathi, S. R., Franke, K., Wernersson, S., Babina, M., & Hellman, L. (2024) · Cells · doi:10.3390/cells13010098 · Cited by 9

Novel indoline derivatives prevent inflammation and ulceration in dinitro-benzene sulfonic acid-induced colitis in rats

Shifrin, H., Moradov, D., Bejar, C., Schorer-Apelbaum, D., & Weinstock, M. (2016) · Pharmacological Reports · doi:10.1016/j.pharep.2016.08.008 · Cited by 9

How Microbial Food Fermentation Supports a Tolerant Gut

Poppe, J., van Baarle, L., Matteoli, G., & Verbeke, K. (2020) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.202000036 · Cited by 9

Behind the monocyte’s mystique: uncovering their developmental trajectories and fates

Teh, Y. C., Chooi, M. Y., & Chong, S. Z. (2023) · Discovery Immunology · doi:10.1093/discim/kyad008 · Cited by 12

Microbiome and Gut Immunity: Innate Immune Cells

Strowig, T., Thiemann, S., & Diefenbach, A. (2018) · Springer eBooks · doi:10.1007/978-3-319-90545-7_8 · Cited by 9

Opportunities and Challenges for Single-Unit Recordings from Enteric Neurons in Awake Animals

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The Conversion of Human Tissue‐Like Inflammatory Monocytes Into Macrophages

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