Efferocytosis in health and disease
Open accessAbstract
The clearance of apoptotic cells by professional and non-professional phagocytes - a process termed 'efferocytosis' - is essential for the maintenance of tissue homeostasis. Accordingly, defective efferocytosis underlies a growing list of chronic inflammatory diseases. Although much has been learnt about the mechanisms of apoptotic cell recognition and uptake, several key areas remain incompletely understood. This Review focuses on new discoveries related to how phagocytes process the metabolic cargo they receive during apoptotic cell uptake; the links between efferocytosis and the resolution of inflammation in health and disease; and the roles of efferocytosis in host defence. Understanding these aspects of efferocytosis sheds light on key physiological and pathophysiological processes and suggests novel therapeutic strategies for diseases driven by defective efferocytosis and impaired inflammation resolution.
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Efferocytosis in other settings can promote fibrosis as part of tissue resolution, for example, by secreting TGF-β1.
“efferocytosis in other settings can promote fibrosis as part of the tissue resolution process, for example, by secreting TGF-β1 (12, 13).”
From Impaired TIM4-mediated efferocytosis by liver macrophages contributes to fibrosis in metabolic dysfunction–associated steatohepatitis (2025) · cites this paper as [12]
The Conclusions (page unavailable) say a fibrotic response can follow efferocytosis. In “Myocardial infarction and heart failure” (page unavailable), the review says efferocytic myofibroblasts upregulate Tgfb and that their TGFβ production may promote excessive fibrosis. It does not establish secretion of TGF-β1 specifically or characterize that fibrosis as part of tissue resolution; it cautions that the fibrosis may be harmful. (LLM, conf=0.86)
Experimental — accuracy not yet measuredAccumulation of dead cells in disease indicates impaired clearance by macrophages.
“The accumulation of dead cells in disease settings indicates impaired clearance of dead cells by macrophages (“efferocytosis”) (12, 13).”
From Impaired TIM4-mediated efferocytosis by liver macrophages contributes to fibrosis in metabolic dysfunction–associated steatohepatitis (2025) · cites this paper as [12]
Efferocytosis prevents dead cell accumulation and reprograms macrophages for tissue resolution, and its impairment contributes to many chronic inflammatory diseases.
“Efferocytosis not only prevents dead cell accumulation but also reprograms macrophages to execute tissue resolution functions, and impaired efferocytosis contributes to many human chronic inflammatory diseases (12, 13).”
From Impaired TIM4-mediated efferocytosis by liver macrophages contributes to fibrosis in metabolic dysfunction–associated steatohepatitis (2025) · cites this paper as [12]
Efferocytosis can reprogram macrophages toward a proresolving, disease-suppressing state.
“Efferocytosis can reprogram macrophages to a proresolving, disease-suppressing state (12, 39)”
From Impaired TIM4-mediated efferocytosis by liver macrophages contributes to fibrosis in metabolic dysfunction–associated steatohepatitis (2025) · cites this paper as [12]
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2 retracted
Martinez, J., Malireddi, R. K. S., Lu, Q., Cunha, L. D., Pelletier, S., Gingras, S., Orchard, R., Guan, J.-L., Tan, H., Peng, J., et al. (2015) · Nature Cell Biology · doi:10.1038/ncb3192 · Cited by 758 · see citing works
RetractedMartinez, J., Almendinger, J., Oberst, A., Ness, R., Dillon, C. P., Fitzgerald, P., Hengartner, M. O., & Green, D. R. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1113421108 · Cited by 655 · see citing works
RetractedFadok, 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 · see citing works
Regulatory T cells: mechanisms of differentiation and function
Josefowicz, S. Z., Lu, L.-F., & Rudensky, A. Y. (2012) · Annual Review of Immunology · doi:10.1146/annurev.immunol.25.022106.141623 · Cited by 2,866 · see citing works
Macrophages in the Pathogenesis of Atherosclerosis
Moore, K. J., & Tabas, I. (2011) · Cell · doi:10.1016/j.cell.2011.04.005 · Cited by 2,669 · see citing works
Self-citationDendritic cells acquire antigen from apoptotic cells and induce class I-restricted CTLs
Albert, M. L., Sauter, B., & Bhardwaj, N. (1998) · Nature · doi:10.1038/32183 · Cited by 2,350 · see citing works
Immunosuppressive effects of apoptotic cells
Voll, R. E., Herrmann, M., Roth, E. A., Stach, C., Kalden, J. R., & Girkontaite, I. (1997) · Nature · doi:10.1038/37022 · Cited by 1,787 · see citing works
Nucleotides released by apoptotic cells act as a find-me signal to promote phagocytic clearance
Elliott, M. R., Chekeni, F. B., Trampont, P. C., Lazarowski, E. R., Kadl, A., Walk, S. F., Park, D., Woodson, R. I., Ostankovich, M., Sharma, P., et al. (2009) · Nature · doi:10.1038/nature08296 · Cited by 1,654 · see citing works
Corpse clearance defines the meaning of cell death
Savill, J., & Fadok, V. A. (2000) · Nature · doi:10.1038/35037722 · Cited by 1,535 · see citing works
Endocytosis and the recycling of plasma membrane.
Steinman, R. M., Mellman, I., Müller, W. A., & Cohn, Z. A. (1983) · The Journal of Cell Biology · doi:10.1083/jcb.96.1.1 · Cited by 1,453 · see citing works
Homozygous C1q deficiency causes glomerulonephritis associated with multiple apoptotic bodies
Botto, M., Dell' Agnola, C., Bygrave, A. E., Thompson, E. M., Cook, H. T., Petry, F., Loos, M., Pandolfi, P. P., & Walport, M. J. (1998) · Nature Genetics · doi:10.1038/ng0598-56 · Cited by 1,434 · see citing works
Inflammation and its resolution in atherosclerosis: mediators and therapeutic opportunities
Bäck, M., Yurdagul, A., Tabas, I., Öörni, K., & Kovanen, P. T. (2019) · Nature Reviews Cardiology · doi:10.1038/s41569-019-0169-2 · Cited by 1,341 · see citing works
Self-citationApoptotic cell clearance: basic biology and therapeutic potential
Poon, I. K. H., Lucas, C. D., Rossi, A. G., & Ravichandran, K. S. (2014) · Nature Reviews Immunology · doi:10.1038/nri3607 · Cited by 1,223 · see citing works
Phagocytosis and clearance of apoptotic cells is mediated by MER
Scott, R. S., McMahon, E. J., Pop, S. M., Reap, E. A., Caricchio, R., Cohen, P. L., Earp, H. S., & Matsushima, G. K. (2001) · Nature · doi:10.1038/35075603 · Cited by 1,215 · see citing works
Immunogenic and tolerogenic cell death
Green, D. R., Ferguson, T., Zitvogel, L., & Kroemer, G. (2009) · Nature Reviews Immunology · doi:10.1038/nri2545 · Cited by 1,176 · see citing works
TAM Receptors Are Pleiotropic Inhibitors of the Innate Immune Response
Rothlin, C. V., Ghosh, S., Zuniga, E. I., Oldstone, M. B. A., & Lemke, G. (2007) · Cell · doi:10.1016/j.cell.2007.10.034 · Cited by 1,055 · see citing works
An estimation of the number of cells in the human body
Bianconi, E., Piovesan, A., Facchin, F., Beraudi, A., Casadei, R., Frabetti, F., Vitale, L., Pelleri, M. C., Tassani, S., Piva, F., et al. (2013) · Annals of Human Biology · doi:10.3109/03014460.2013.807878 · Cited by 1,012 · see citing works
Autoimmune Disease and Impaired Uptake of Apoptotic Cells in MFG-E8-Deficient Mice
Hanayama, R., Tanaka, M., Miyasaka, K., Aozasa, K., Koike, M., Uchiyama, Y., & Nagata, S. (2004) · Science · doi:10.1126/science.1094359 · Cited by 992 · see citing works
Phagocytosis of apoptotic cells in homeostasis
Arandjelovic, S., & Ravichandran, K. S. (2015) · Nature Immunology · doi:10.1038/ni.3253 · Cited by 959 · see citing works
Metabolic Reprograming in Macrophage Polarization
Galván-Peña, S., & O’Neill, L. A. J. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00420 · Cited by 944 · see citing works
CD4 + CD25 + Foxp3 + regulatory T cells induce alternative activation of human monocytes/macrophages
Tiemessen, M. M., Jagger, A. L., Evans, H. G., van Herwijnen, M. J. C., John, S., & Taams, L. S. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0706832104 · Cited by 856 · see citing works
BAI1 is an engulfment receptor for apoptotic cells upstream of the ELMO/Dock180/Rac module
Park, D., Tosello‐Trampont, A., Elliott, M. R., Lu, M., Haney, L. B., Ma, Z., Klibanov, A. L., Mandell, J. W., & Ravichandran, K. S. (2007) · Nature · doi:10.1038/nature06329 · Cited by 848 · see citing works
Inflammation and plaque vulnerability
Hansson, G. K., Libby, P., & Tabas, I. A. (2015) · Journal of Internal Medicine · doi:10.1111/joim.12406 · Cited by 809 · see citing works
Self-citationVaccinia Virus Uses Macropinocytosis and Apoptotic Mimicry to Enter Host Cells
Mercer, J., & Helenius, A. (2008) · Science · doi:10.1126/science.1155164 · Cited by 784 · see citing works
Ichimura, T., van Asseldonk, E. J. P., Humphreys, B. D., Gunaratnam, L., Duffield, J. S., & Bonventre, J. V. (2008) · Journal of Clinical Investigation · doi:10.1172/jci34487 · Cited by 768 · see citing works
Boulter, L., Govaere, O., Bird, T. G., Radulescu, S., Ramachandran, P., Pellicoro, A., Ridgway, R. A., Seo, S. S., Spee, B., Van Rooijen, N., et al. (2012) · Nature Medicine · doi:10.1038/nm.2667 · Cited by 747 · see citing works
Resolvin D1 binds human phagocytes with evidence for proresolving receptors
Krishnamoorthy, S., Recchiuti, A., Chiang, N., Yacoubian, S., Lee, C., Yang, R., Petasis, N. A., & Serhan, C. N. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907342107 · Cited by 738 · see citing works
Horckmans, M., Ring, L., Duchêne, J., Santovito, D., Schloss, M. J., Drechsler, M. D., Weber, C., Soehnlein, O., & Steffens, S. (2016) · European Heart Journal · doi:10.1093/eurheartj/ehw002 · Cited by 737 · see citing works
WAVE, a novel WASP‐family protein involved in actin reorganization induced by Rac
Miki, H., Suetsugu, S., & Takenawa, T. (1998) · The EMBO Journal · doi:10.1093/emboj/17.23.6932 · Cited by 709 · see citing works
Weirather, J., Hofmann, U., Beyersdorf, N., Ramos, G. C., Vogel, B., Frey, A., Ertl, G., Kerkau, T., & Frantz, S. (2014) · Circulation Research · doi:10.1161/circresaha.115.303895 · Cited by 705 · see citing works
Macrophage Dysfunction Impairs Resolution of Inflammation in the Wounds of Diabetic Mice
Khanna, S., Biswas, S., Shang, Y., Collard, E., Azad, A., Kauh, C., Bhasker, V., Gordillo, G. M., Sen, C. K., & Roy, S. (2010) · PLoS ONE · doi:10.1371/journal.pone.0009539 · Cited by 694 · see citing works
Fadok, V., de Cathelineau, A., Daleke, D. L., Henson, P., & Bratton, D. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m003649200 · Cited by 689 · see citing works
CD47-blocking antibodies restore phagocytosis and prevent atherosclerosis
Kojima, Y., Volkmer, J.-P., McKenna, K., Civelek, M., Lusis, A. J., Miller, C. L., Direnzo, D., Nanda, V., Ye, J., Connolly, A. J., et al. (2016) · Nature · doi:10.1038/nature18935 · Cited by 683 · see citing works
A-González, N., Bensinger, S. J., Hong, C., Beceiro, S., Bradley, M. N., Zelcer, N., Deniz, J. M., Ramírez, C. M., Díaz, M., Gallardo, G., et al. (2009) · Immunity · doi:10.1016/j.immuni.2009.06.018 · Cited by 674 · see citing works
Geng, Y., & Libby, P. (1995) · PubMed · Cited by 641 · see citing works
Godson, C., Mitchell, S., Harvey, K., Petasis, N. A., Hogg, N., & Brady, H. R. (2000) · The Journal of Immunology · doi:10.4049/jimmunol.164.4.1663 · Cited by 638 · see citing works
Phagocytosis and innate immunity
Greenberg, S., & Grinstein, S. (2002) · Current Opinion in Immunology · doi:10.1016/s0952-7915(01)00309-0 · Cited by 581 · see citing works
Ghisletti, S., Huang, W., Ogawa, S., Pascual, G., Lin, M.-E., Willson, T. M., Rosenfeld, M. G., & Glass, C. K. (2007) · Molecular Cell · doi:10.1016/j.molcel.2006.11.022 · Cited by 561 · see citing works
Dalli, J., & Serhan, C. N. (2012) · Blood · doi:10.1182/blood-2012-04-423525 · Cited by 556 · see citing works
Apoptosis facilitates antigen presentation to T lymphocytes through MHC-I and CD1 in tuberculosis
Schaible, U. E., Winau, F., Sieling, P. A., Fischer, K., Collins, H. L., Hagens, K., Modlin, R. L., Brinkmann, V., & Kaufmann, S. H. E. (2003) · Nature Medicine · doi:10.1038/nm906 · Cited by 546 · see citing works
Phagocytosis of apoptotic cells by macrophages is impaired in atherosclerosis
Schrijvers, D. M., De Meyer, G. R. Y., Kockx, M. M., Herman, A. G., & Martinet, W. (2005) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/01.atv.0000166517.18801.a7 · Cited by 509 · see citing works
Clearing the Dead: Apoptotic Cell Sensing, Recognition, Engulfment, and Digestion
Hochreiter-Hufford, A., & Ravichandran, K. S. (2013) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a008748 · Cited by 503 · see citing works
Zhang, S., Weinberg, S., DeBerge, M., Gainullina, A., Schipma, M., Kinchen, J. M., Ben-Sahra, I., Gius, D. R., Yvan-Charvet, L., Chandel, N. S., et al. (2019) · Cell Metabolism · doi:10.1016/j.cmet.2018.12.004 · Cited by 485 · see citing works
CX3CL1/fractalkine is released from apoptotic lymphocytes to stimulate macrophage chemotaxis
Truman, L. A., Ford, C. A., Pasikowska, M., Pound, J. D., Wilkinson, S. J., Dumitriu, I. E., Melville, L., Melrose, L. A., Ogden, C. A., Nibbs, R., et al. (2008) · Blood · doi:10.1182/blood-2008-06-162404 · Cited by 473 · see citing works
Rapid cell corpse clearance by stabilin-2, a membrane phosphatidylserine receptor
Park, S.-Y., Jung, M.-Y., Kim, H.-J., Lee, S., Kim, S.-Y., Lee, B.-H., Kwon, T.-H., Park, R. W., & Kim, I. T. (2007) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4402242 · Cited by 464 · see citing works
Uptake of apoptotic cells drives the growth of a pathogenic trypanosome in macrophages
Freire-de-Lima, C. G., Nascimento, D. O., Soares, M. B. P., Bozza, P. T., Castro-Faria-Neto, H. C., Mello, F. G. D., DosReis, G. A., & Lopes, M. F. (2000) · Nature · doi:10.1038/35003208 · Cited by 455 · see citing works
Regulatory T Cells Promote Macrophage Efferocytosis during Inflammation Resolution
Proto, J. D., Doran, A. C., Gusarova, G., Yurdagul, A., Sozen, E., Subramanian, M., Islam, M. N., Rymond, C. C., Du, J., Hook, J., et al. (2018) · Immunity · doi:10.1016/j.immuni.2018.07.015 · Cited by 441 · see citing works
Self-citationEfferocytosis Signaling in the Regulation of Macrophage Inflammatory Responses
Elliott, M. R., Koster, K. M., & Murphy, P. S. (2017) · The Journal of Immunology · doi:10.4049/jimmunol.1601520 · Cited by 440 · see citing works
Fredman, G., Hellmann, J., Proto, J. D., Kuriakose, G., Colas, R. A., Dorweiler, B., Connolly, E. S., Solomon, R., Jones, D. M., Heyer, E. J., et al. (2016) · Nature Communications · doi:10.1038/ncomms12859 · Cited by 411 · see citing works
Self-citationJorgensen, I., Zhang, Y., Krantz, B. A., & Miao, E. A. (2016) · Journal of Experimental Medicine · doi:10.1084/jem.20151613 · Cited by 403 · see citing works
Apoptotic cell removal in development and tissue homeostasis
Henson, P. M., & Hume, D. A. (2006) · Trends in Immunology · doi:10.1016/j.it.2006.03.005 · Cited by 388 · see citing works
Identification of resolvin D2 receptor mediating resolution of infections and organ protection
Chiang, N., Dalli, J., Colas, R. A., & Serhan, C. N. (2015) · The Journal of Experimental Medicine · doi:10.1084/jem.20150225 · Cited by 388 · see citing works
Wan, E. Y., Yeap, X. Y., Dehn, S., Terry, R. L., Novak, M. L., Zhang, S., Iwata, S., Han, X., Homma, S., Drosatos, K., et al. (2013) · Circulation Research · doi:10.1161/circresaha.113.301198 · Cited by 385 · see citing works
Efferocytosis induces a novel SLC program to promote glucose uptake and lactate release
Morioka, S., Perry, J. S. A., Raymond, M. H., Medina, C. B., Zhu, Y., Zhao, L., Serbulea, V., Önengüt-Gümüşcü, S., Leitinger, N., Kucenas, S., et al. (2018) · Nature · doi:10.1038/s41586-018-0735-5 · Cited by 370 · see citing works
KIM-1–mediated phagocytosis reduces acute injury to the kidney
Yang, L., Brooks, C. R., Xiao, S., et al. (2015) · Journal of Clinical Investigation · doi:10.1172/jci75417 · Cited by 368 · see citing works
PPAR-δ senses and orchestrates clearance of apoptotic cells to promote tolerance
Mukundan, L., Odegaard, J. I., Morel, C. R., Heredia, J. E., Mwangi, J. W., Ricardo-Gonzalez, R. R., Goh, Y. P. S., Eagle, A. R., Dunn, S. E., Awakuni, J. U. H., et al. (2009) · Nature Medicine · doi:10.1038/nm.2048 · Cited by 368 · see citing works
Innate immune recognition of infected apoptotic cells directs TH17 cell differentiation
Torchinsky, M. B., Garaude, J., Martin, A. P., & Blander, J. M. (2009) · Nature · doi:10.1038/nature07781 · Cited by 364 · see citing works
Gude, D., Alvarez, S. E., Paugh, S. W., Mitra, P., Yu, J., Griffiths, R., Barbour, S. E., Milstien, S., & Spiegel, S. (2008) · The FASEB Journal · doi:10.1096/fj.08-107169 · Cited by 364 · see citing works
Mitochondrial fission promotes the continued clearance of apoptotic cells by macrophages
Wang, Y., Subramanian, M., Yurdagul, A., Barbosa-Lorenzi, V. C., Cai, B., de Juan-Sanz, J., Ryan, T. A., Nomura, M., Maxfield, F. R., & Tabas, I. (2017) · Cell · doi:10.1016/j.cell.2017.08.041 · Cited by 364 · see citing works
Self-citationFredman, G., Kamaly, N., Spolitu, S., Milton, J., Ghorpade, D. S., Chiasson, R., Kuriakose, G., Perretti, M., Farokhzad, O. C., & Tabas, I. A. (2015) · Science Translational Medicine · doi:10.1126/scitranslmed.aaa1065 · Cited by 360 · see citing works
Self-citationThorp, E., Cui, D., Schrijvers, D. M., Kuriakose, G., & Tabas, I. (2008) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.108.167197 · Cited by 357 · see citing works
Self-citationSather, S., Kenyon, K. D., Lefkowitz, J. B., Liang, X., Varnum, B. C., Henson, P. M., & Graham, D. K. (2006) · Blood · doi:10.1182/blood-2006-05-021634 · Cited by 333 · see citing works
TGF-β: Guardian of T Cell Function
Oh, S. A., & Li, M. O. (2013) · The Journal of Immunology · doi:10.4049/jimmunol.1301843 · Cited by 320 · see citing works
The Dynamics of Apoptotic Cell Clearance
Elliott, M. R., & Ravichandran, K. S. (2016) · Developmental Cell · doi:10.1016/j.devcel.2016.06.029 · Cited by 314 · see citing works
Mechanisms and Consequences of Defective Efferocytosis in Atherosclerosis
Yurdagul, A., Doran, A. C., Cai, B., Fredman, G., & Tabas, I. A. (2018) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2017.00086 · Cited by 300 · see citing works
Self-citationThorp, E., Vaisar, T., Subramanian, M., Mautner, L., Blobel, C., & Tabas, I. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.263020 · Cited by 298 · see citing works
Self-citationLiu, M., O’Connor, R. S., Trefely, S., Graham, K. L., Snyder, N. W., & Beatty, G. L. (2019) · Nature Immunology · doi:10.1038/s41590-018-0292-y · Cited by 294 · see citing works
IL-10 Potentiates Differentiation of Human Induced Regulatory T Cells via STAT3 and Foxo1
Hsu, P. S., Santner‐Nanan, B., Hu, M., Skarratt, K. K., Lee, C. H., Stormon, M., Wong, M., Fuller, S. J., & Nanan, R. K. H. (2015) · The Journal of Immunology · doi:10.4049/jimmunol.1402898 · Cited by 288 · see citing works
Mitchell, S., Thomas, G., Harvey, K., Cottell, D., Reville, K., Berlasconi, G., Petasis, N. A., Erwig, L., Rees, A. J., Savill, J., et al. (2002) · Journal of the American Society of Nephrology · doi:10.1097/01.asn.0000032417.73640.72 · Cited by 287 · see citing works
Efferocytosis Is an Innate Antibacterial Mechanism
Martin, C. J., Booty, M. G., Rosebrock, T. R., Nunes-Alves, C., Desjardins, D. M., Keren, I., Fortune, S. M., Remold, H. G., & Behar, S. M. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.06.010 · Cited by 285 · see citing works
The role of non-resolving inflammation in atherosclerosis
Kasikara, C., Doran, A. C., Cai, B., & Tabas, I. (2018) · Journal of Clinical Investigation · doi:10.1172/jci97950 · Cited by 266 · see citing works
Self-citationMerTK receptor cleavage promotes plaque necrosis and defective resolution in atherosclerosis
Cai, B., Thorp, E. B., Doran, A. C., Sansbury, B. E., Daemen, M. J. A. P., Dorweiler, B., Spite, M., Fredman, G., & Tabas, I. (2017) · Journal of Clinical Investigation · doi:10.1172/jci90520 · Cited by 262 · see citing works
Self-citationMerTK cleavage limits proresolving mediator biosynthesis and exacerbates tissue inflammation
Cai, B., Thorp, E. B., Doran, A. C., Subramanian, M., Sansbury, B. E., Lin, C., Spite, M. R., Fredman, G., & Tabas, I. A. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1524292113 · Cited by 253 · see citing works
Self-citationTwist mediates suppression of inflammation by type I IFNs and Axl
Sharif, M. N., Šošić, D., Rothlin, C. V., Kelly, E., Lemke, G., Olson, E. N., & Ivashkiv, L. B. (2006) · The Journal of Experimental Medicine · doi:10.1084/jem.20051725 · Cited by 251 · see citing works
Continued clearance of apoptotic cells critically depends on the phagocyte Ucp2 protein
Park, D., Han, C. Z., Elliott, M. R., Kinchen, J. M., Trampont, P. C., Das, S., Collins, S., Lysiak, J. J., Hoehn, K. L., & Ravichandran, K. S. (2011) · Nature · doi:10.1038/nature10340 · Cited by 250 · see citing works
Resolvin D3 and Aspirin-Triggered Resolvin D3 Are Potent Immunoresolvents
Dalli, J., Winkler, J. W., Colas, R. A., Arnardottir, H. H., Cheng, C.-Y. C., Chiang, N., Petasis, N. A., & Serhan, C. N. (2013) · Chemistry & Biology · doi:10.1016/j.chembiol.2012.11.010 · Cited by 246 · see citing works
Yrlid, U., & Wick, M. J. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.191.4.613 · Cited by 244 · see citing works
DeBerge, M., Yeap, X. Y., Dehn, S., Zhang, S., Grigoryeva, L. S., Misener, S., Procissi, D., Zhou, X., Lee, D. C., Müller, W. A., et al. (2017) · Circulation Research · doi:10.1161/circresaha.117.311327 · Cited by 241 · see citing works
Self-citationApoptotic cells induce Mer tyrosine kinase–dependent blockade of NF-κB activation in dendritic cells
Sen, P., Wallet, M. A., Yi, Z., Huang, Y., Henderson, M., Mathews, C. E., Earp, H. S., Matsushima, G. K., Baldwin, A. S., & Tisch, R. (2006) · Blood · doi:10.1182/blood-2006-04-017368 · Cited by 237 · see citing works
Schif‐Zuck, S., Gross, N., Assi, S., Rostoker, R., Serhan, C. N., & Ariel, A. (2010) · European Journal of Immunology · doi:10.1002/eji.201040801 · Cited by 236 · see citing works
Dallenga, T. K., Repnik, U., Corleis, B., Eich, J., Reimer, R., Griffiths, G. W., & Schaible, U. E. (2017) · Cell Host & Microbe · doi:10.1016/j.chom.2017.09.003 · Cited by 231 · see citing works
Erythropoeitin Signaling in Macrophages Promotes Dying Cell Clearance and Immune Tolerance
Luo, B., Gan, W., Liu, Z., Shen, Z., Wang, J., Shi, R., Liu, Y., Liu, Y., Jiang, M., Zhang, Z., et al. (2016) · Immunity · doi:10.1016/j.immuni.2016.01.002 · Cited by 229 · see citing works
Different tissue phagocytes sample apoptotic cells to direct distinct homeostasis programs
Cummings, R. J., Barbet, G., Bongers, G., Hartmann, B. M., Gettler, K., Muniz, L., Furtado, G. C., Cho, J., Lira, S. A., & Blander, J. M. (2016) · Nature · doi:10.1038/nature20138 · Cited by 228 · see citing works
Phagocytosis of apoptotic cells and the resolution of inflammation
MADERNA, P., & Godson, C. (2003) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2003.09.004 · Cited by 223 · see citing works
Contrasting phagosome pH regulation and Maturation in Human M1 and M2 macrophages
Canton, J., Khezri, R., Glogauer, M., & Grinstein, S. (2014) · Molecular Biology of the Cell · doi:10.1091/mbc.e14-05-0967 · Cited by 221 · see citing works
Loynes, C. A., Lee, J. A., Robertson, A. L., Steel, M. J., Ellett, F. E., Feng, Y., Levy, B. D., Whyte, M. K. B., & Renshaw, S. A. (2018) · Science Advances · doi:10.1126/sciadv.aar8320 · Cited by 221 · see citing works
Ye, Z.-M., Yang, S., Xia, Y., Hu, R., Chen, S., Li, B., Chen, S.-L., Luo, X., Mao, L., Li, Y., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1409-4 · Cited by 208 · see citing works
Otsuka, F., Kramer, M. C. A., Woudstra, P., Yahagi, K., Ladich, E. R., Finn, A. V., de Winter, R. J., Kolodgie, F. D., Wight, T. N., Davis, H. R., et al. (2015) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2015.05.011 · Cited by 199 · see citing works
Cholesterol in health and disease
Tabas, I. A. (2002) · Journal of Clinical Investigation · doi:10.1172/jci0216381 · Cited by 190 · see citing works
Self-citationAit-Oufella, H., Pouresmail, V., Simon, T., Blanc-Brude, O., Kinugawa, K., Merval, R., Offenstadt, G., Lesèche, G., Cohen, P. L., Tedgui, A., et al. (2008) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.108.169078 · Cited by 187 · see citing works
Greenlee‐Wacker, M. C., Rigby, K. M., Kobayashi, S. D., Porter, A. R., DeLeo, F. R., & Nauseef, W. M. (2014) · The Journal of Immunology · doi:10.4049/jimmunol.1302692 · Cited by 185 · see citing works
Ariel, A., & Serhan, C. N. (2012) · Frontiers in Immunology · doi:10.3389/fimmu.2012.00004 · Cited by 184 · see citing works
Macrophages clean up: efferocytosis and microbial control
Martin, C. J., Peters, K. N., & Behar, S. M. (2013) · Current Opinion in Microbiology · doi:10.1016/j.mib.2013.10.007 · Cited by 177 · see citing works
The Role of TLR2, TLR4, and TLR9 in the Pathogenesis of Atherosclerosis
Roshan, M. H. K., Tambo, A., & Pace, N. P. (2016) · International Journal of Inflammation · doi:10.1155/2016/1532832 · Cited by 177 · see citing works
Cai, B., Kasikara, C., Doran, A. C., Ramakrishnan, R., Birge, R. B., & Tabas, I. (2018) · Science Signaling · doi:10.1126/scisignal.aar3721 · Cited by 175 · see citing works
Self-citationBoosting Inflammation Resolution in Atherosclerosis
Fredman, G., & Tabas, I. A. (2017) · American Journal Of Pathology · doi:10.1016/j.ajpath.2017.01.018 · Cited by 173 · see citing works
Self-citationBosnjak, L., Miranda‐Saksena, M., Koelle, D. M., et al. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.4.2220 · Cited by 169 · see citing works
Macrophage LRP-1 Controls Plaque Cellularity by Regulating Efferocytosis and Akt Activation
Yancey, P. G., Blakemore, J., Ding, L., Fan, D., Overton, C. D., Zhang, Y., Linton, M. F., & Fazio, S. (2010) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.109.202051 · Cited by 168 · see citing works
Li, S., Sun, Y., Liang, C., Thorp, E. B., Han, S., Jehle, A. W., Saraswathi, V., Pridgen, B. C., Kanter, J. E., Li, R., et al. (2009) · Circulation Research · doi:10.1161/circresaha.109.199570 · Cited by 168 · see citing works
Self-citationCholesterol in health and disease
Tabas, I. A. (2002) · Journal of Clinical Investigation · doi:10.1172/jci16381 · Cited by 167 · see citing works
Self-citationCa2+ and synaptotagmin VII–dependent delivery of lysosomal membrane to nascent phagosomes
Czibener, C., Sherer, N. M., Becker, S. M., Pypaert, M., Hui, E., Chapman, E. R., Mothes, W., & Andrews, N. W. (2006) · The Journal of Cell Biology · doi:10.1083/jcb.200605004 · Cited by 165 · see citing works
Deletion of Macrophage LDL Receptor–Related Protein Increases Atherogenesis in the Mouse
Overton, C. D., Yancey, P. G., Major, A. S., Linton, M. F., & Fazio, S. (2007) · Circulation Research · doi:10.1161/01.res.0000260204.40510.aa · Cited by 159 · see citing works
Apoptotic Cells Deliver Processed Antigen to Dendritic Cells for Cross-Presentation
Blachère, N. E., Darnell, R. B., & Albert, M. L. (2005) · PLoS Biology · doi:10.1371/journal.pbio.0030185 · Cited by 153 · see citing works
Membrane recruitment of Rac1 triggers phagocytosis
Castellano, F., Montcourrier, P., & Chavrier, P. (2000) · Journal of Cell Science · doi:10.1242/jcs.113.17.2955 · Cited by 153 · see citing works
Intravenous apoptotic spleen cell infusion induces a TGF-β-dependent regulatory T-cell expansion
Kleinclauss, F., Perruche, S., Masson, E., Bittencourt, M. D. C., Biichlé, S., Remy-Martin, J.-P., Ferrand, C., Martin, M., Bittard, H., Chalopin, J. M., et al. (2005) · Cell Death and Differentiation · doi:10.1038/sj.cdd.4401699 · Cited by 146 · see citing works
Metabolic Connections during Apoptotic Cell Engulfment
Han, C. Z., & Ravichandran, K. S. (2011) · Cell · doi:10.1016/j.cell.2011.12.006 · Cited by 144 · see citing works
Liver X receptors as regulators of macrophage inflammatory and metabolic pathways
A-González, N., & Castrillo, A. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2010.12.015 · Cited by 139 · see citing works
Cardiac myofibroblast engulfment of dead cells facilitates recovery after myocardial infarction
Nakaya, M., Watari, K., Tajima, M., Nakaya, T., Matsuda, S., Ohara, H., Nishihara, H., Yamaguchi, H., Hashimoto, A. S., Nishida, M., et al. (2016) · Journal of Clinical Investigation · doi:10.1172/jci83822 · Cited by 136 · see citing works
Fernandez-Boyanapalli, R. F., Frasch, S. C., McPhillips, K. A., Vandivier, R. W., Harry, B. L., Riches, D. W. H., Henson, P. M., & Bratton, D. L. (2008) · Blood · doi:10.1182/blood-2008-05-160564 · Cited by 133 · see citing works
T Cell Zone Resident Macrophages Silently Dispose of Apoptotic Cells in the Lymph Node
Baratin, M., Simon, L., Jorquera, A., Ghigo, C., Dembélé, D., Nowak, J., Gentek, R., Wienert, S., Klauschen, F., MALISSEN, B., et al. (2017) · Immunity · doi:10.1016/j.immuni.2017.07.019 · Cited by 131 · see citing works
Resolvin D1 promotes the targeting and clearance of necroptotic cells
Gerlach, B. D., Marinello, M., Heinz, J., Rymut, N., Sansbury, B. E., Riley, C. O., Sadhu, S., Hosseini, Z., Kojima, Y., Tang, D. D., et al. (2019) · Cell Death and Differentiation · doi:10.1038/s41418-019-0370-1 · Cited by 128 · see citing works
Differential use of endoplasmic reticulum membrane for phagocytosis in J774 macrophages
Becker, T., Volchuk, A., & Rothman, J. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0409219102 · Cited by 125 · see citing works
Impaired Clearance of Apoptotic Cells in Chronic Inflammatory Diseases: Therapeutic Implications
Szondy, Z., Garabuczi, Ã., Joós, G., Tsay, G. J., & Sarang, Z. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00354 · Cited by 124 · see citing works
An AXL/LRP-1/RANBP9 complex mediates DC efferocytosis and antigen cross-presentation in vivo
Subramanian, M., Hayes, C. D., Thome, J. J. C., Thorp, E. B., Matsushima, G. K., Herz, J., Färber, D. L., Liu, K., Lakshmana, M. K., & Tabas, I. A. (2014) · Journal of Clinical Investigation · doi:10.1172/jci72051 · Cited by 123 · see citing works
Self-citationMaekawa, T., Hosur, K. B., Abe, T., Kantarcı, A., Ziogas, A., Wang, B., Dyke, T. E. V., Chavakis, T., & Hajishengallis, G. (2015) · Nature Communications · doi:10.1038/ncomms9272 · Cited by 121 · see citing works
Macrophage Proresolving Mediators—the When and Where
Dalli, J., & Serhan, C. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.mchd-0001-2014 · Cited by 121 · see citing works
Larsson, M., Fonteneau, J., Lirvall, M., et al. (2002) · AIDS · doi:10.1097/00002030-200207050-00003 · Cited by 120 · see citing works
Lysosomal Cholesterol Hydrolysis Couples Efferocytosis to Anti-Inflammatory Oxysterol Production
Viaud, M., Ivanov, S., Vujić, N., Duta-Mare, M., Aira, L., Barouillet, T., Garcia, E., Orange, F., Dugail, I., Hainault, I., et al. (2018) · Circulation Research · doi:10.1161/circresaha.117.312333 · Cited by 120 · see citing works
Apoptotic Cells Induce a Phosphatidylserine-Dependent Homeostatic Response from Phagocytes
Kiss, R. S., Elliott, M. R., Ma, Z., Marcel, Y. L., & Ravichandran, K. S. (2006) · Current Biology · doi:10.1016/j.cub.2006.09.043 · Cited by 119 · see citing works
Suresh Babu, S., Thandavarayan, R. A., Joladarashi, D., Jeyabal, P., Krishnamurthy, S., Bhimaraj, A., Youker, K. A., & Krishnamurthy, P. (2016) · Scientific Reports · doi:10.1038/srep36207 · Cited by 119 · see citing works
Apoptotic cells trigger a membrane-initiated pathway to increase ABCA1
Fond, A. M., Lee, C. S., Schulman, I. G., Kiss, R. S., & Ravichandran, K. S. (2015) · Journal of Clinical Investigation · doi:10.1172/jci80300 · Cited by 114 · see citing works
Doran, A. C., Özcan, L., Cai, B., Zheng, Z., Fredman, G., Rymond, C. C., Dorweiler, B., Sluimer, J. C., Hsieh, J., Kuriakose, G., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci94735 · Cited by 113 · see citing works
Self-citationJennewein, C., Kühn, A., Schmidt, M. V., Meilladec-Jullig, V., von Knethen, A., Gonzalez, F. J., & Brüne, B. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.181.8.5646 · Cited by 110 · see citing works
Cell death and autophagy in tuberculosis
Moraco, A. H., & Kornfeld, H. (2014) · Seminars in Immunology · doi:10.1016/j.smim.2014.10.001 · Cited by 106 · see citing works
Requirement of Adaptor Protein GULP during Stabilin-2-mediated Cell Corpse Engulfment
Park, S., Kang, K.-B., Thapa, N., Kim, S.-Y., Lee, S.-J., & Kim, I. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.m709105200 · Cited by 105 · see citing works
Apoptosis in response to microbial infection induces autoreactive TH17 cells
Campisi, L., Barbet, G., Ding, Y., Esplugues, E., Flavell, R. A., & Blander, J. M. (2016) · Nature Immunology · doi:10.1038/ni.3512 · Cited by 105 · see citing works
The innate immune system and the clearance of apoptotic cells
Devitt, A., & Marshall, L. J. (2011) · Journal of Leukocyte Biology · doi:10.1189/jlb.0211095 · Cited by 103 · see citing works
Xian, X., Ding, Y., Dieckmann, M., Zhou, L., Plattner, F., Liu, M., Parks, J. S., Hammer, R. E., Boucher, P., Tsai, S. X., et al. (2017) · eLife · doi:10.7554/elife.29292 · Cited by 103 · see citing works
Jondle, C. N., Gupta, K., Mishra, B. B., & Sharma, J. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1007338 · Cited by 101 · see citing works
Arrode, G., Boccaccio, C., Lulé, J., et al. (2000) · Journal of Virology · doi:10.1128/jvi.74.21.10018-10024.2000 · Cited by 95 · see citing works
Tzelepis, F., Verway, M. J., Daoud, J., Gillard, J., Hassani‐Ardakani, K., Dunn, J. L., Downey, J., Gentile, M., Jaworska, J., Sanchez, A. M. J., et al. (2014) · Journal of Clinical Investigation · doi:10.1172/jci77014 · Cited by 93 · see citing works
Efferocytosis and autoimmune disease
Kawano, M., & Nagata, S. (2018) · International Immunology · doi:10.1093/intimm/dxy055 · Cited by 89 · see citing works
Driscoll, W. S., Vaisar, T., Tang, J., Wilson, C. L., & Raines, E. W. (2013) · Circulation Research · doi:10.1161/circresaha.112.300683 · Cited by 87 · see citing works
Rinne, P., Guillamat‐Prats, R., Rami, M., Bîndilă, L., Ring, L., Lyytikäinen, L., Raitoharju, E., Oksala, N., Lehtimäki, T. J., Weber, C., et al. (2018) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.118.311185 · Cited by 87 · see citing works
Mechanism of Enhanced MerTK-Dependent Macrophage Efferocytosis by Extracellular Vesicles
de Couto, G., Jaghatspanyan, E., DeBerge, M., Liu, W., Luther, K. M., Wang, Y., Tang, J., Thorp, E. B., & Marbán, E. (2019) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.119.313115 · Cited by 85 · see citing works
The many ways tissue phagocytes respond to dying cells
Blander, J. M. (2017) · Immunological Reviews · doi:10.1111/imr.12537 · Cited by 84 · see citing works
How to Eat Something Bigger than Your Head
Aderem, A. A. (2002) · Cell · doi:10.1016/s0092-8674(02)00819-x · Cited by 83 · see citing works
Yancey, P. G., Ding, Y., Fan, D., Blakemore, J. L., Zhang, Y., Ding, L., Zhang, J., Linton, M. F., & Fazio, S. (2011) · Circulation · doi:10.1161/circulationaha.111.032268 · Cited by 83 · see citing works
Maxed out macs: physiologic cell clearance as a function of macrophage phagocytic capacity
Zent, C. S., & Elliott, M. R. (2016) · FEBS Journal · doi:10.1111/febs.13961 · Cited by 79 · see citing works
Campbell‐Valois, F., Trost, M., Chemali, M., Dill, B. D., Laplante, A., Duclos, S., Sadeghi, S., Rondeau, C., Morrow, I. C., Bell, C., et al. (2012) · Molecular & Cellular Proteomics · doi:10.1074/mcp.m111.016378 · Cited by 77 · see citing works
Zhang, Y., Wang, Y., Zhou, D. F., Zhang, L.-S., Deng, F., Shu, S., Wang, L., Wu, Y., Guo, N., Zhou, J., et al. (2019) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00145.2019 · Cited by 76 · see citing works
Cui, D., Thorp, E., Li, Y., Wang, N., Yvan-Charvet, L., Tall, A. R., & Tabas, I. (2007) · Journal of Leukocyte Biology · doi:10.1189/jlb.0307192 · Cited by 73 · see citing works
Self-citationGarbin, U., Baggio, E., Stranieri, C., Pasini, A., Manfro, S., Mozzini, C., Vallerio, P., Lipari, G., Merigo, F., Guidi, G. C., et al. (2012) · Cardiovascular Research · doi:10.1093/cvr/cvs301 · Cited by 72 · see citing works
Brophy, M. L., Dong, Y., Tao, H., Yancey, P. G., Song, K., Zhang, K., Wen, A., Wu, H., Lee, Y., Malovichko, M. V., et al. (2018) · Circulation Research · doi:10.1161/circresaha.118.313028 · Cited by 65 · see citing works
Zhang, S., Yeap, X., DeBerge, M., Naresh, N. K., Wang, K., Jiang, Z., Wilcox, J. E., White, S. M., Morrow, J., Burridge, P. W., et al. (2017) · JACC Basic to Translational Science · doi:10.1016/j.jacbts.2017.03.013 · Cited by 63 · see citing works
Attraction of phagocytes by apoptotic cells is mediated by lysophosphatidylcholine
Müeller, R. B., Sheriff, A., Gaipl, U. S., Wesselborg, S., & Lauber, K. (2007) · Autoimmunity · doi:10.1080/08916930701356911 · Cited by 62 · see citing works
Myc‐nick promotes efferocytosis through M2 macrophage polarization during resolution of inflammation
Zhong, X., Lee, H., Kim, S. H., Park, S., Kim, W., Cha, Y., & Surh, Y. (2018) · The FASEB Journal · doi:10.1096/fj.201800223r · Cited by 62 · see citing works
Lumbroso, D., Soboh, S., Maimon, A., Schif‐Zuck, S., Ariel, A., & Burstyn‐Cohen, T. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00358 · Cited by 62 · see citing works
Rab17 mediates differential antigen sorting following efferocytosis and phagocytosis
Yin, C., Kim, Y., Argintaru, D., & Heit, B. (2016) · Cell Death and Disease · doi:10.1038/cddis.2016.431 · Cited by 55 · see citing works
Evans, I. R., Ghai, P. A., Urbančič, V., Tan, K. L., & Wood, W. (2013) · Cell Death and Differentiation · doi:10.1038/cdd.2012.166 · Cited by 53 · see citing works
Codo, A. C., Saraiva, A. C., dos Santos, L. L., Visconde, M. F., Gales, A. C., Zamboni, D. S., & de Medeiros, A. I. (2018) · Cell Death and Disease · doi:10.1038/s41419-018-1214-5 · Cited by 49 · see citing works
Tajbakhsh, A., Hayat, S. M. G., Butler, A. E., & Sahebkar, A. (2019) · Ageing Research Reviews · doi:10.1016/j.arr.2019.01.007 · Cited by 49 · see citing works
Thymosin β4 is involved in stabilin‐2‐mediated apoptotic cell engulfment
Lee, S.-J., So, I.-S., Park, S., & Kim, I. (2008) · FEBS Letters · doi:10.1016/j.febslet.2008.03.058 · Cited by 48 · see citing works
Luo, B., Wang, Z., Zhang, Z., Shen, Z., & Zhang, Z. (2018) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2018.10.005 · Cited by 42 · see citing works
Dejani, N. N., Orlando, A. B., Niño-Castaño, V. E., Penteado, L. D. A., Verdan, F. F., Bazzano, J. M. R., Codo, A. C., Salina, A. C. G., Saraiva, A. C., Avelar, M. R., et al. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1722016115 · Cited by 41 · see citing works
Lumbroso, D., Soboh, S., Maimon, A., Schif‐Zuck, S., Ariel, A., & Burstyn‐Cohen, T. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.412281 · Cited by 40 · see citing works
Increased lymphocyte activation and atherosclerosis in CD47-deficient mice
Engelbertsen, D., Autio, A. K., Verwilligen, R. A. F., Depuydt, M. A. C., Newton, G. A., Rattik, S., Levinsohn, E. A., Saggu, G., Jarolı́m, P., Wang, H., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-46942-x · Cited by 32 · see citing works
Salina, A. C. G., de Souza, T. P., Serezani, C. H., & de Medeiros, A. I. (2016) · Innate Immunity · doi:10.1177/1753425916684934 · Cited by 28 · see citing works
Manega, C. M., Fiorelli, S., Porro, B., Turnu, L., Cavalca, V., Bonomi, A., Cosentino, N., Minno, A. D., Marenzi, G., Tremoli, E., et al. (2019) · Pharmacological Research · doi:10.1016/j.phrs.2019.03.012 · Cited by 28 · see citing works
Penteado, L. D. A., Dejani, N. N., Verdan, F. F., Orlando, A. B., Niño-Castaño, V. E., Dias, F. D. N., Salina, A. C. G., & de Medeiros, A. I. (2017) · Immunology · doi:10.1111/imm.12731 · Cited by 27 · see citing works
Blander, J. M., Torchinsky, M. B., & Campisi, L. (2012) · Immunologic Research · doi:10.1007/s12026-012-8311-9 · Cited by 25 · see citing works
Rab17 mediates intermixing of phagocytosed apoptotic cells with recycling endosomes
Yin, C., Argintaru, D., & Heit, B. (2017) · Small GTPases · doi:10.1080/21541248.2017.1308852 · Cited by 24 · see citing works
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Mehrotra, P., & Ravichandran, K. S. (2022) · Nature Reviews Drug Discovery · doi:10.1038/s41573-022-00470-y · Cited by 459 · see citing works
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Gerlach, B. D., Ampomah, P. B., Yurdagul, A., Liu, C., Lauring, M. C., Wang, X., Kasikara, C., Kong, N., Shi, J., Tao, W., et al. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.10.015 · Cited by 360 · see citing works
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Podleśny-Drabiniok, A., Marcora, E., & Goate, A. M. (2020) · Trends in Neurosciences · doi:10.1016/j.tins.2020.10.002 · Cited by 211 · see citing works
Mederacke, I., Filliol, A., Affo, S., Nair, A., Hernandez, C., Sun, Q., Hamberger, F., Brundu, F., Chen, Y., Ravichandra, A., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abe5795 · Cited by 103 · see citing works
Self-citationShi, H., Wang, X., Li, F., Gerlach, B. D., Yurdagul, A., Moore, M. P., Zeldin, S., Zhang, H., Cai, B., Zheng, Z., et al. (2022) · Science Translational Medicine · doi:10.1126/scitranslmed.abp8309 · Cited by 85 · see citing works
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- Authors
- Doran, A. C., Yurdagul, A., & Tabas, I.
- Affiliations
- Vanderbilt University (US)
- Columbia University Irving Medical Center (US)
- Corresponding author
- Tabas, Ira
- Venue
- Nature Reviews Immunology
- Published
- 2019-12-10
- Volume
- 20
- Issue
- 4
- Pages
- 254-267
- ISSN
- 1474-1733 (ISSN-L)
- 1474-1741
- PMC
- PMC7667664
- OpenAlex
- W2995149669
- Cited by
- 1,066
- References
- 163
- Citations by year
- 2026: 208 · 2025: 240 · 2024: 184 · 2023: 174 · 2022: 125 · 2021: 93 · 2020: 42
- FWCI
- 5.60
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature reviews. Immunology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Heart, Lung, and Blood Institute (K99HL145131, R01HL127464, P01HL087123, R35HL145228)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Phagocytosis and Immune Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
- Keywords
- efferocytosis, phagocytes, tissue homeostasis, inflammation resolution, chronic inflammatory diseases, apoptotic cell recognition, host defense, treatment options
- MeSH terms
- Homeostasis, Humans, Inflammation, Phagocytes, Phagocytosis, Apoptosis
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 ›
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