The DOI matches its Crossref record; 31 of the 31 references it cites were found in a registry or an index.
Phagocytosis and clearance of apoptotic cells is mediated by MER
Abstract
Apoptosis is fundamental to the development and maintenance of animal tissues and the immune system. Rapid clearance of apoptotic cells by macrophages is important to inhibit inflammation and autoimmune responses against intracellular antigens. Here we report a new function for Mer, a member of the Axl/Mer/Tyro3 receptor tyrosine kinase family. mer(kd) mice with a cytoplasmic truncation of Mer had macrophages deficient in the clearance of apoptotic thymocytes. This was corrected in chimaeric mice reconstituted with bone marrow from wild-type animals. Primary macrophages isolated from mer(kd) mice showed that the phagocytic deficiency was restricted to apoptotic cells and was independent of Fc receptor-mediated phagocytosis or ingestion of other particles. The inability to clear apoptotic cells adequately may be linked to an increased number of nuclear autoantibodies in mer(kd) mice. Thus, the Mer receptor tyrosine kinase seems to be critical for the engulfment and efficient clearance of apoptotic cells. This has implications for inflammation and autoimmune diseases such as systemic lupus erythematosus.
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
“In general, MERTK plays a key role in a variety of phagocytic events, such as microglial phagocytosis to mediate synaptic pruning (Chung et al., 2013), macrophage phagocytosis to remove apoptotic immune cells (Scott et al., 2001), and phagocytosis of apoptotic germ cells and the residual body from maturing sperm by Sertoli cells in the testes (Breucker et al., 1985).”
From The cell biology of the retinal pigment epithelium (2020) · cites this paper as Scott et al., 2001
Citations
Cites
Fadok, V. A., Voelker, D. R., Campbell, P. A., Cohen, J., Bratton, D. L., & Henson, P. M. (1992) · The Journal of Immunology · doi:10.4049/jimmunol.148.7.2207 · Cited by 3,321
Programmed Cell Death in Animal Development
Jacobson, M. D., Weil, M., & RAFF, M. C. (1997) · Cell · doi:10.1016/s0092-8674(00)81873-5 · Cited by 2,685
A receptor for phosphatidylserine-specific clearance of apoptotic cells
Fadok, V. A., Bratton, D. L., Rose, D. M., Pearson, A. M., Ezekowitz, R. A. B., & Henson, P. M. (2000) · Nature · doi:10.1038/35011084 · Cited by 1,491
Phagocyte recognition of cells undergoing apoptosis
Savill, J., Fadok, V. A., Henson, P. M., & Haslett, C. (1993) · Immunology Today · doi:10.1016/0167-5699(93)90215-7 · Cited by 981
Mutation of the receptor tyrosine kinase gene Mertk in the retinal dystrophic RCS rat
D'Cruz, P. M. (2000) · Human Molecular Genetics · doi:10.1093/hmg/9.4.645 · Cited by 884
Vitronectin receptor-mediated phagocytosis of cells undergoing apoptosis
Savill, J., Dransfield, I., Hogg, N., & Haslett, C. (1990) · Nature · doi:10.1038/343170a0 · Cited by 846
Savill, J., Hogg, N., Ren, Y., & Haslett, C. (1992) · Journal of Clinical Investigation · doi:10.1172/jci116019 · Cited by 818
O’Bryan, J. P., Frye, R. A., Cogswell, P. C., Neubauer, A., Kitch, B., Prokop, C. A., Espinosa, R., Beau, M. M. L., Earp, H. S., & Liu, E. (1991) · Molecular and Cellular Biology · doi:10.1128/mcb.11.10.5016 · Cited by 746
Taylor, P. R., Carugati, A., Fadok, V. A., Cook, H. T., Andrews, M., Carroll, M. C., Savill, J., Henson, P. M., Botto, M., & Walport, M. J. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.3.359 · Cited by 724
Human CD14 mediates recognition and phagocytosis of apoptotic cells
Devitt, A., Moffatt, O., Raykundalia, C., Capra, J. D., Simmons, D. L., & Gregory, C. D. (1998) · Nature · doi:10.1038/33169 · Cited by 681
Flagged first, then by citations
Cited by
Sorted by citations
Items 901–1,000 of 1,000
Anti-Atherogenic Mechanisms and Therapies
Hudson, A., Igiehon, O. O., Woolard, M. D., & Yurdagul, A. (2025) · Current Atherosclerosis Reports · doi:10.1007/s11883-025-01324-9 · Cited by 7
Ultrastructural Changes in Endothelium during Apoptosis Indicate Low Microembolic Potential
Xu, W., Boadle, R. A., Dear, L., Cvejic, M., Emmanuel, C., & Zoellner, H. F. (2005) · Journal of Vascular Research · doi:10.1159/000087213 · Cited by 7
Assessing Efferocytosis in Atherosclerotic Lesions In Situ.
Yurdagul, A. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-1924-7_34 · Cited by 6
Ryu, K., Pokhrel, N. K., Jung, H.-J., Kim, H. J., Seok, J., Kim, T. Y., Kim, H. J., Lee, J. H., Kim, J., Kim, Y., et al. (2024) · JBMR Plus · doi:10.1093/jbmrpl/ziad014 · Cited by 7
Efferocytosis and inflammation: a bibliometric and systematic analysis
Cao, X., Li, F., Xie, X. S., Ling, G., Tang, X., He, W., Tian, J., & Ge, Y. (2025) · Frontiers in Medicine · doi:10.3389/fmed.2025.1498503 · Cited by 7
Liphaus, B., Kiss, M., Carrasco, S., & Goldenstein‐Schainberg, C. (2013) · Lupus · doi:10.1177/0961203313496300 · Cited by 7
Allergy: Airway Epithelial Rac1 Suppresses Allergic Inflammation
Henson, P. M., & Bratton, D. L. (2013) · Current Biology · doi:10.1016/j.cub.2012.12.008 · Cited by 7
Recent advances into the role of pattern recognition receptors in transplantation
Kulkarni, H. S., Scozzi, D., & Gelman, A. E. (2020) · Cellular Immunology · doi:10.1016/j.cellimm.2020.104088 · Cited by 7
Park, T. H., Bae, S.-H., Bong, S. M., Ryu, S. E., Jang, H., & Lee, B. I. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21217878 · Cited by 7
MERTK retinopathy: biomarkers assessing vision loss
Sakti, D. H., Cornish, E. E., Mustafic, N., Zaheer, A., Retsas, S., Rajagopalan, S., Chung, C. W. T., Ewans, L., McCluskey, P., Nash, B. M., et al. (2021) · Ophthalmic Genetics · doi:10.1080/13816810.2021.1955278 · Cited by 7
Recognition and Removal of Apoptotic Cells
Henson, P. M., & Bratton, D. L. (2014) · ASM Press eBooks · doi:10.1128/9781555816650.ch21 · Cited by 7
A Presumed Human Nuclear Autoantigen That Translocates to Plasma Membrane Blebs during Apoptosis
Shiratsuchi, A. (2003) · The Journal of Biochemistry · doi:10.1093/jb/mvg026 · Cited by 7
Lawman, S. H. A., & Ehrenstein, M. R. (2002) · Lupus · doi:10.1191/0961203302lu301rr · Cited by 6
Pathogenesis of Cutaneous Lupus Erythematosus: The Role of Ultraviolet Light
Rosenbaum, M. L., & Werth, V. P. (2005) · Springer eBooks · doi:10.1007/3-540-26581-3_18 · Cited by 7
Experimental models of systemic lupus erythematosus: anti-dsDNA in murine lupus
Blank, M., & Shoenfeld, Y. (2005) · Lara D. Veeken · doi:10.1093/rheumatology/keh695 · Cited by 7
Recent advances in TAM mechanisms in lung diseases
Ban, J.-Q., Qian, J., Zhang, C., & Li, J. (2025) · Journal of Translational Medicine · doi:10.1186/s12967-025-06398-2 · Cited by 7
The Role of Extracellular Vesicles in Efferocytosis
Panahi, S., Yazdi, Z. R., Sanchouli, M., Sajadi, F., Motavasselian, F., Abed, H. M., Beygi, Z., & Hayat, S. M. G. (2023) · Mini-Reviews in Medicinal Chemistry · doi:10.2174/0113895575247690230926113455 · Cited by 6
Guillet, S., Lazarov, T., Jordan, N., Boisson, B., Tello‐Lafoz, M., Craddock, B. P., Zhou, T., Nishi, C., Bareja, R., Yang, H., et al. (2024) · eLife · doi:10.7554/elife.96085.3 · Cited by 7
Physiology of cellular demise: Apoptosis, necrosis, and autophagy
Kaur, D., & Deshmukh, R. R. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-815762-6.00002-0 · Cited by 10
Apoptotic Cells Trigger Calcium Entry in Phagocytes by Inducing the Orai1-STIM1 Association
Kim, D., Moon, H., Cho, H., Min, C., Moon, B., Yang, S., Lee, J., Lee, S.-A., Park, H.-J., Lee, D.-H., et al. (2021) · Cells · doi:10.3390/cells10102702 · Cited by 6
MERTK in the rat trigeminal system: a potential novel target for cluster headache?
Edvinsson, J. C. A., Ran, C., Olofsgård, F. J., Steinberg, A., Edvinsson, L. I., & Belin, A. C. (2024) · The Journal of Headache and Pain · doi:10.1186/s10194-024-01791-6 · Cited by 6
The SH3 regulatory domain of the hematopoietic cell kinase Hck binds ELMO via its polyproline motif
Awad, R., Sevajol, M., Ayala, I., Chouquet, A., Frachet, P., Gans, P., Reiser, J., & Kleman, J.-P. (2015) · FEBS Open Bio · doi:10.1016/j.fob.2015.01.009 · Cited by 7
Sequence‐specific binding of normal serum immunoglobulin M to exposed protein C‐termini
Sokoloff, A. V., Puckett, M., Ludtke, J. J., & Fetterly, B. (2004) · Immunology · doi:10.1111/j.1365-2567.2004.01868.x · Cited by 6
Post-translational modifications of the ligands: Requirement for TAM receptor activation
Geng, K. (2020) · International review of cytology · doi:10.1016/bs.ircmb.2020.09.002 · Cited by 7
Autophagic cell death in viral infection: Do TAM receptors play a role?
Datan, E., & Salman, S. (2020) · International review of cytology · doi:10.1016/bs.ircmb.2020.10.001 · Cited by 5
Small Molecule Inhibitors of MERTK and FLT3 Induce Cell Cycle Arrest in Human CD8+ T Cells
Powell, R., Peeters, M. J. W., Rahbech, A., Aehnlich, P., Seremet, T., & Straten, P. T. (2021) · Vaccines · doi:10.3390/vaccines9111294 · Cited by 5
Iadevaia, V., Rinaldi, A., Falasca, L., Pucillo, L. P., Alonzi, T., Chimini, G., & Piacentini, M. (2006) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401930 · Cited by 6
Results of Defective Clearance of Apoptotic Cells: Lessons from Knock-out Mouse Models
Gregory, C. D., & Pound, J. D. (2009) · Springer eBooks · doi:10.1007/978-1-4020-9293-0_9 · Cited by 6
L’élimination des cellules apoptotiques : une phagocytose particulière
Alibert, M., & Chimini, G. (2002) · médecine/sciences · doi:10.1051/medsci/20021889853 · Cited by 6
Groos, S., Busche, R., Engelhardt, W. V., Reale, E., & Luciano, L. (2004) · Cell and Tissue Research · doi:10.1007/s00441-004-0853-2 · Cited by 6
Mitochondrial hyperpolarization and ATP depletion in patients with systemic lupus erythematosus
Gergely, P., Grossman, C., Niland, B., Puskas, F., Neupane, H., Allam, F., Banki, K., Phillips, P. E., & Perl, A. (2002) · Arthritis & Rheumatism · doi:10.1002/1529-0131(200201)46:1 · Cited by 5
He, Z., Chen, N., Zhang, Y., Du, H., & Jie, L. (2026) · Journal of Inflammation Research · doi:10.2147/jir.s582297 · Cited by 7
Walsh, A. D., Johnson, L., Harvey, A. J., Kilpatrick, T. J., & Binder, M. D. (2020) · Brain Plasticity · doi:10.3233/bpl-200102 · Cited by 5
Qi, X., Guo, H., Xia, X., Liu, Y., Qiu, S., Lin, T., He, W., Jin, L., Cheng, J., Hao, L., et al. (2025) · International Immunopharmacology · doi:10.1016/j.intimp.2025.114571 · Cited by 6
Animal Models: Systemic Autoimmune Diseases
Mizui, M., & Tsokos, G. C. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-812102-3.00029-4 · Cited by 5
Coagulopathies and inflammatory diseases: ‘…glimpse of a Snark’
del Carmen, S., Hapak, S. M., Ghosh, S., & Rothlin, C. V. (2018) · Current Opinion in Immunology · doi:10.1016/j.coi.2018.09.005 · Cited by 5
Multiple Sclerosis as a Syndrome—Implications for Future Management
Dwyer, C., Nguyen, L. T.-T., Healy, L. M., Dutta, R., Ludwin, S. K., Antel, J. P., Binder, M. D., & Kilpatrick, T. J. (2020) · Frontiers in Neurology · doi:10.3389/fneur.2020.00784 · Cited by 5
Phagocyte Chemoattraction Is Induced through the Mcp-1–Ccr2 Axis during Efferocytosis
Lee, S.-A., Kim, D., Min, C., Moon, B., Lee, J., Moon, H., Yang, S., Lee, C. S., Lee, G., & Park, D. (2021) · Cells · doi:10.3390/cells10113115 · Cited by 5
Molecules Involved in Recognition and Clearance of Apoptotic/Necrotic Cells and Cell Debris
Napirei, M., & Mannherz, H. G. (2009) · Springer eBooks · doi:10.1007/978-1-4020-9293-0_4 · Cited by 5
Imaging a concussion and the ensuing immune response at the blood–brain barrier
Nguyen, R., Newton, M., Kratofil, R. M., Scott, B. N. V., Castanheira, F. V. S., Kim, J., Ginhoux, F., Jung, S., & Kubes, P. (2025) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2414316122 · Cited by 4
Engineering Efferocytosis for Bone Regeneration
Miszuk, J. M., Zhong, L., & Sun, H. (2025) · Macromolecular Bioscience · doi:10.1002/mabi.202500094 · Cited by 5
Gao, M., Zhou, J., Shi, N., Yan, X., & Liang, L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1742677 · Cited by 5
Zheng, A., Liu, H., Yin, G., & Xie, Q. (2025) · Immunologic Research · doi:10.1007/s12026-025-09723-5 · Cited by 6
Jain, S., & Shah, N. (2010) · Clinical Pharmacology Advances and Applications · doi:10.2147/cpaa.s11366 · Cited by 4
Chronicles of Cell Death Foretold: Specificities in the Mechanism of Disposal
Hughes, L. D., Bosurgi, L., Ghosh, S., & Rothlin, C. V. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01743 · Cited by 4
Signal Mechanisms of M2 Macrophage Activation
Rőszer, T. (2020) · Progress in inflammation research · doi:10.1007/978-3-030-50480-9_4 · Cited by 4
Genes and Gene Therapy in Inherited Retinal Disease
Shughoury, A., Ciulla, T. A., Bakall, B., Pennesi, M. E., Kiss, S., & Cunningham, E. T. (2021) · International Ophthalmology Clinics · doi:10.1097/iio.0000000000000377 · Cited by 4
Pelé, T., Giraud, S., Joffrion, S., Ameteau, V., Delwail, A., Goujon, J., Macchi, L., Hauet, T., Dkhissi, F., & Benzakour, O. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms222212103 · Cited by 4
Diversity in Phagocytic Signaling
García-García, E. (2008) · Springer eBooks · doi:10.1007/978-0-387-28669-3_1 · Cited by 4
Naik, U., & Harrison, R. E. (2013) · Colloquium Series on Building Blocks of the Cell Cell Structure and Function · doi:10.4199/c00081ed1v01y201304bbc004 · Cited by 3
Lacy‐Hulbert, A. (2009) · Springer eBooks · doi:10.1007/978-1-4020-9293-0_7 · Cited by 3
Maintenance of self-tolerance by apoptotic cell clearance
Tanaka, M. (2008) · Frontiers in bioscience · doi:10.2741/3135 · Cited by 4
The role of apoptosis and removal of apoptotic cells in the genesis of systemic lupus erythematosus
Fransen, J. H., Hilbrands, L. B., Koeter, C. M., & van der Vlag, J. (2009) · Cited by 4
Chloroquine Treatment Increases Detection of 5-Fluorouracil-Induced Apoptosis In Vivo
Nyati, M. K., Feng, F. Y.-C., Kanade, V. D., & Nayak, R. (2006) · Molecular Imaging · doi:10.2310/7290.2006.00017 · Cited by 4
Atherogenesis: The Development of Stable and Unstable Plaques
Mori, H., Finn, A. V., Kolodgie, F. D., Davis, H. R., Joner, M., & Virmani, R. (2017) · Springer eBooks · doi:10.1007/978-1-4471-5245-3_2 · Cited by 4
Crucial role of Mer tyrosine kinase in the maintenance of SIGN ‐R1+ marginal zone macrophages
Soni, C., Schell, S. L., Fasnacht, M. J., Chodisetti, S. B., & Rahman, Z. S. M. (2018) · Immunology and Cell Biology · doi:10.1111/imcb.12003 · Cited by 4
Wang, X., & Frye, S. V. (2014) · Annual reports in medicinal chemistry · doi:10.1016/b978-0-12-800167-7.00019-5 · Cited by 5
Zandman‐Goddard, G., & Blank, M. (2002) · PubMed · Cited by 4
Pollalis, D., Georgescu, C., Wren, J. D., Tombulyan, G., Leung, J., Lo, P.-A., Bloemhof, C. M., Lee, R. H., Bae, E., Bailey, J., et al. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.04.09.588773 · Cited by 4
Guillet, S., Lazarov, T., Jordan, N., Boisson, B., Tello‐Lafoz, M., Craddock, B. P., Zhou, T., Nishi, C., Bareja, R., Yang, H., et al. (2024) · eLife · doi:10.7554/elife.96085.2.sa0 · Cited by 3
Negro‐Demontel, M. L., Evans, F., Cawen, F. A., Fitzpatrick, Z., Mason, H. D., Alí‐Ruiz, D., López‐Vales, R., Lago, N., & Peluffo, H. (2025) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2025.106105 · Cited by 5
Progress of ADAM17 in Fibrosis‐Related Diseases
Yan, S., Zhao, Y., Yang, Y., Liu, B., Xu, W., Ma, Z., & Yang, Q. (2025) · Mediators of Inflammation · doi:10.1155/mi/9999723 · Cited by 4
Opposing role of phagocytic receptors MERTK and AXL in Progranulin deficient FTD
Clelland, C. D., Fan, L., Saloner, R., Etchegaray, J. I., Altobelli, C. R., Salomonsson, S. E., Birk, A. M., Sachdev, A., Zhu, J., Lee, S.-I., et al. (2025) · Communications Biology · doi:10.1038/s42003-025-08368-2 · Cited by 4
Serum growth arrest specific protein 6 and its receptor (Axl) in SLE patients
Bakr, S. I., Fedawy, S. F. E., Abbas, A. A., Shedid, N. H., & Ahmed, S. F. (2014) · The Egyptian Rheumatologist · doi:10.1016/j.ejr.2014.07.003 · Cited by 3
Cell Proliferation, Survival, Necrosis and Apoptosis
Mierke, C. T. (2020) · Biological and medical physics, biomedical engineering · doi:10.1007/978-3-030-58532-7_16 · Cited by 3
Su, C., Himes, J. E., & Kirsch, D. G. (2023) · International review of cytology · doi:10.1016/bs.ircmb.2023.03.006 · Cited by 3
Shi, H., Zhang, Z., Yuan, X., Liu, G., Fan, W., & Wang, W. (2024) · Aging · doi:10.18632/aging.205732 · Cited by 3
Lemke, G. (2015) · Springer eBooks · doi:10.1007/978-3-319-11888-8_2 · Cited by 3
Inhibitory Immunoreceptors on Mast Cells in Allergy and Inflammation
Shibuya, A., Nakahashi-Oda, C., & Tahara‐Hanaoka, S. (2015) · Springer eBooks · doi:10.1007/978-4-431-55651-0_8 · Cited by 3
A Possible Link Between Autoimmunity and Cancer
Cristaldi, E., Malaguarnera, G., Rando, A., & Malaguarner, M. (2011) · InTech eBooks · doi:10.5772/23988 · Cited by 3
Efferocytosis in Retinoblastoma
Das, D., Bhattacharjee, H., Bhattacharjee, K., Tahiliani, P. S., Bhattacharyya, P., Barman, M., Barthakur, S. S., Deka, P., Deka, A., & Paul, R. (2013) · Journal of Cancer Therapy · doi:10.4236/jct.2013.49172 · Cited by 3
Beug, S. T., Vascotto, S. G., & Tsilfidis, C. (2006) · Developmental Dynamics · doi:10.1002/dvdy.20690 · Cited by 3
Engineering cross-presentation in vivo
Chattergoon, M. A., Shames, J. P., & Weiner, D. B. (2003) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.3.6.887 · Cited by 3
Origin and Distribution of Durum Wheat Genetic Diversity in the World
Bozzini, A., David, J., & Natoli, V. (2012) · Elsevier eBooks · doi:10.1016/b978-1-891127-65-6.50006-4 · Cited by 3
Qi, G., Hua, H., Gao, Y., Lin, Q., & Yu, G. (2007) · Chinese Medical Journal · doi:10.1097/00029330-200708020-00009 · Cited by 3
Emerging roles of tyrosine kinases in hepatic inflammatory diseases and therapeutic opportunities
Shaker, M. E., Gomaa, H. A. M., Abdelgawad, M. A., El‐Mesery, M., Shaaban, A. A., & Hazem, S. H. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.110373 · Cited by 3
Proteases from Inflammatory Cells: Regulation of Inflammatory Response
Pederzoli-Ribeil, M., Gabillet, J., & Witko‐Sarsat, V. (2011) · Springer eBooks · doi:10.1007/978-3-0348-0157-7_4 · Cited by 3
Ray, D., & Richardson, B. C. (2012) · doi:10.1002/9781118349045.ch13 · Cited by 3
Silverman, G. J. (2010) · Arthritis Research & Therapy · doi:10.1186/ar3162 · Cited by 3
Guttenberg, M. A., Vose, A. T., Birukova, A., Lewars, K., Cumming, R. I., Albright, M. C., Mark, J. I., Salazar, C. J., Swaminathan, S., Yu, Z., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.11.06.565865 · Cited by 3
Efferocytosis: a therapeutic strategy for diabetes and its vascular complications
Song, Y., Yuan, J., Li, Y., Liu, Y., & Qin, G. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1641748 · Cited by 2
Takeda, S., Sridhar, S., Schefer, D., Andreu-Agulló, C., Lo, P. C., Lee, M., Busby, R. W., Darst, D. M., Assmus, A., Anaganti, S., et al. (2026) · Cancer Research · doi:10.1158/0008-5472.can-25-2998 · Cited by 2
Myeloid Piezo1 Drives Cardiac Repair Through Orai1–Rac1-Dependent Efferocytosis
Liu, S., Xu, H., Deng, B., Jiang, J., He, Y., Fang, C., Zhang, Z., Pan, X., Luo, S., Wan, R., et al. (2026) · Circulation Research · doi:10.1161/circresaha.125.328012 · Cited by 2
Liang, R., Shaker, E., Zhao, M., King, G. E., & Moalli, P. (2024) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2024.02.282 · Cited by 3
Roux, E., Willms, R. J., Dycke, J. V., Calabuig, Á. C., Espen, L. V., Schoofs, G., Matthijnssens, J., Neyts, J. H., de Witte, P. A. M., Foley, E., et al. (2024) · Gut Microbes · doi:10.1080/19490976.2024.2431167 · Cited by 2
Autoimmune Diseases and the Role of MFG-E8
Hanayama, R. (2014) · Springer eBooks · doi:10.1007/978-94-017-8765-9_6 · Cited by 2
Immune Regulation by Dead Cell Clearance
Tanaka, M., & Nishitai, G. (2015) · Current topics in microbiology and immunology · doi:10.1007/82_2015_472 · Cited by 2
Autoimmunity, Atherosclerosis and Apoptotic Cell Clearance
Aprahamian, T. R. (2012) · InTech eBooks · doi:10.5772/25575 · Cited by 2
Lyar Is a New Ligand for Retinal Pigment Epithelial Phagocytosis
Guo, F., Ding, Y., Caberoy, N. B., Alvarado, G., Liu, R., Shen, C., Yu, J., Zhou, Y., Salero, E., LeBlanc, M. E., et al. (2015) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25089 · Cited by 2
Ito, M., Omoto, S., Kato, Y., Hayashi, T., Mori, N., & Fujii, Y. R. (2005) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2005.02809.x · Cited by 2
Phagocytosis: Invitation to a Feast
Henson, P. M. (2009) · Current Biology · doi:10.1016/j.cub.2009.09.031 · Cited by 2
Drug discovery in academic institutions
Frye, S. V. (2013) · Hematology · doi:10.1182/asheducation-2013.1.300 · Cited by 2
Role of Mertk in RPE Phagocytosis and Retinal Disease
Vollrath, D., & Feng, W. (2004) · WORLD SCIENTIFIC eBooks · doi:10.1142/9789812561756_0013 · Cited by 2
Animal Models of Autoimmune Disease
von Herrath, M., & Tsokos, G. C. (2006) · Elsevier eBooks · doi:10.1016/b978-012595961-2/50029-9 · Cited by 2
Cell Survival and Death in Rheumatic Diseases
Elkon, K. B. (2013) · Elsevier eBooks · doi:10.1016/b978-1-4377-1738-9.00027-x · Cited by 2
PEGylation of anti-MerTK Antibody Modulates Ocular Biodistribution
Vollmar, B. S., Fei, M., Liang, W., Bravo, D. D., Wang, J., Yu, L., Corr, N., Zhang, G., McNamara, E., Masih, S., et al. (2022) · Bioconjugate Chemistry · doi:10.1021/acs.bioconjchem.2c00276 · Cited by 2
Targeted Phagocytosis Induction for Cancer Immunotherapy via Bispecific MerTK-Engaging Antibodies
Carrara, S. C., Bogen, J. P., Fiebig, D., Grzeschik, J., Hock, B. M., & Kolmar, H. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms232415673 · Cited by 2
Yan, L., Chen, C., Wang, L., Hong, H., Wu, C., Huang, J., Jiang, J., Chen, J., Xu, G., & Cui, Z. (2024) · Experimental and Therapeutic Medicine · doi:10.3892/etm.2024.12581 · Cited by 2
MerTK signaling in human primary T cells modulates memory potential and improves recall response
Rahbech, A., Kurzay, A., Saló, S. F., Seremet, T., Debets, R., Met, Ö., Peeters, M. J. W., & Straten, P. T. (2024) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiae226 · Cited by 2
Interaction Between Dendritic Cells and Apoptotic Cells
Larregina, A. T., & Morelli, A. E. (2006) · doi:10.1002/9783527619696.ch29 · Cited by 2
Metadata
- Authors
- Scott, R. S., McMahon, E. J., Pop, S. M., Reap, E. A., Caricchio, R., Cohen, P. L., Earp, H. S., & Matsushima, G. K.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- AlphaVax (United States) (US)
- University of Pennsylvania (US)
- UNC Lineberger Comprehensive Cancer Center (US)
- Corresponding author
- Matsushima, Glenn K.
- Venue
- Nature
- Published
- 2001-05
- Volume
- 411
- Issue
- 6834
- Pages
- 207-211
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2011617127
- Cited by
- 1,215
- References
- 31
- Citations by year
- 2026: 27 · 2025: 32 · 2024: 61 · 2023: 44 · 2022: 29 · 2021: 39 · 2020: 61 · 2019: 50 · 2018: 40 · 2017: 50 · 2016: 39 · 2015: 44 · 2014: 60 · 2013: 51 · 2012: 45
- FWCI
- 21.24
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- Research Councils UK
- Biotechnology and Biological Sciences Research Council
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- Mer receptor tyrosine kinase, efferocytosis, phagocytosis, macrophages, systemic lupus erythematosus, autoimmunity, inflammation, thymocytes
- MeSH terms
- c-Mer Tyrosine Kinase, Animals, Antibodies, Antinuclear, Cell Adhesion, Cells, Cultured, Crosses, Genetic, Cytochalasin B, Dexamethasone, Female, Flow Cytometry, Immunohistochemistry, Listeria monocytogenes, Male, Mice, Inbred C57BL, Mice, Mutant Strains, Microscopy, Electron, Scanning, Microspheres, Mutation, Phagocytosis, Protein-Tyrosine Kinases, Proto-Oncogene Proteins, Radiation Chimera, Receptors, Fc, Thymus Gland, Bone Marrow Transplantation, Apoptosis, Macrophages, Peritoneal, Receptor Protein-Tyrosine Kinases, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review