Apoptotic cells trigger a membrane-initiated pathway to increase ABCA1

Heart Disease and Stroke Statistics—2014 Update

Go, A. S., Mozaffarian, D., Roger, V. L., Benjamin, E. J., Berry, J. D., Blaha, M. J., Dai, S., Ford, E. S., Fox, C. S., Franco, S., et al. (2013) · Circulation · doi:10.1161/01.cir.0000441139.02102.80 · Cited by 5,207 · see citing works

CellProfiler: image analysis software for identifying and quantifying cell phenotypes

Carpenter, A. E., Jones, T. R., Lamprecht, M. R., Clarke, C., Kang, I. H., Friman, O., Guertin, D. A., Chang, J. H., Lindquist, R. A., Moffat, J., et al. (2006) · Genome biology · doi:10.1186/gb-2006-7-10-r100 · Cited by 5,077 · see citing works

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

Brooks-Wilson, A., Marcil, M., Clee, S. M., Zhang, L.-H., Roomp, K., van Dam, M., Yu, L., Brewer, C., Collins, J. A., Molhuizen, H. O. F., et al. (1999) · Nature Genetics · doi:10.1038/11905 · Cited by 1,687 · see citing works

Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery.

Ishibashi, S., Brown, M. S., Goldstein, J. L., Gerard, R. D., Hammer, R. E., & Herz, J. (1993) · Journal of Clinical Investigation · doi:10.1172/jci116663 · Cited by 1,612 · see citing works

Role of cholesterol and lipid organization in disease

Maxfield, F. R., & Tabas, I. A. (2005) · Nature · doi:10.1038/nature04399 · Cited by 1,298 · see citing works

Control of cellular cholesterol efflux by the nuclear oxysterol receptor LXRα

Venkateswaran, A., Laffitte, B. A., Joseph, S. B., Mak, P. A., Wilpitz, D. C., Edwards, P. A., & Tontonoz, P. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.200367697 · Cited by 1,005 · see citing works

Autoimmunity and the Clearance of Dead Cells

Nagata, S., Hanayama, R., & Kawane, K. (2010) · Cell · doi:10.1016/j.cell.2010.02.014 · Cited by 877 · 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

Apoptotic Cells Promote Their Own Clearance and Immune Tolerance through Activation of the Nuclear Receptor LXR

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

Metabolic control of cell death

Green, D. R., Galluzzi, L., & Kroemer, G. (2014) · Science · doi:10.1126/science.1250256 · Cited by 661 · see citing works

Engulfment of apoptotic cells: signals for a good meal

Ravichandran, K. S., & Lorenz, U. M. (2007) · Nature reviews. Immunology · doi:10.1038/nri2214 · Cited by 634 · see citing works

Liver X receptors in lipid metabolism: opportunities for drug discovery

Hong, C., & Tontonoz, P. (2014) · Nature Reviews Drug Discovery · doi:10.1038/nrd4280 · Cited by 587 · see citing works

Unconventional Rac-GEF activity is mediated through the Dock180–ELMO complex

Brugnera, E., Haney, L., Grimsley, C., Lu, M., Walk, S. F., Tosello-Trampont, A.-C., Macara, I. G., Madhani, H., Fink, G. R., & Ravichandran, K. S. (2002) · Nature Cell Biology · doi:10.1038/ncb824 · Cited by 576 · see citing works

Molecular Mechanisms of Cellular Cholesterol Efflux

Phillips, M. C. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.r114.583658 · Cited by 546 · see citing works

ATP-Binding Cassette Transporter A1: A Cell Cholesterol Exporter That Protects Against Cardiovascular Disease

Oram, J. F., & Heinecke, J. W. (2005) · Physiological Reviews · doi:10.1152/physrev.00005.2005 · Cited by 521 · see citing works

Cholesterol efflux pathways and other potential mechanisms involved in the athero‐protective effect of high density lipoproteins

Tall, A. R. (2008) · Journal of Internal Medicine · doi:10.1111/j.1365-2796.2007.01898.x · Cited by 436 · see citing works

Dietary induced atherogenesis in swine. Morphology of the intima in prelesion stages.

Gerrity, R. G., Naito, H. K., Richardson, M., & Schwartz, C. J. (1979) · PubMed Central · Cited by 396 · see citing works

Increased Atherosclerosis in Hyperlipidemic Mice With Inactivation of ABCA1 in Macrophages

Aiello, R. J., Brees, D., Bourassa, P.-A., Royer, L., Lindsey, S., Coskran, T., Haghpassand, M., & Francone, O. L. (2002) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/01.atv.0000014804.35824.da · Cited by 390 · see citing works

Leukocyte ABCA1 controls susceptibility to atherosclerosis and macrophage recruitment into tissues

Van Eck, M., Bos, I. S. T., Kaminski, W. E., Orsó, E., Rothe, G., Twisk, J., Böttcher, A., Van Amersfoort, E. S., Christiansen-Weber, T. A., Fung-Leung, W.-P., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.092327399 · Cited by 348 · see citing works

Modulation of Macrophage Efferocytosis in Inflammation

Johnson, D. K., Frasch, S. C., Fernandez-Boyanapalli, R. F., Henson, P. M., & Bratton, D. L. (2011) · Frontiers in Immunology · doi:10.3389/fimmu.2011.00057 · Cited by 346 · see citing works

Rac1 Deletion in Mouse Neutrophils Has Selective Effects on Neutrophil Functions

Glogauer, M., Marchal, C. C., Zhu, F., Worku, A. D., Clausen, B. E., Foerster, I., Marks, P. W., Downey, G. P., Dinauer, M. C., & Kwiatkowski, D. J. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.11.5652 · Cited by 315 · see citing works

Role of ABC transporters in lipid transport and human disease

Tarling, E. J., Vallim, T. Q. D. A., & Edwards, P. A. (2013) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2013.01.006 · Cited by 301 · see citing works

Apoptotic cell clearance by bronchial epithelial cells critically influences airway inflammation

Juncadella, I. J., Kadl, A., Sharma, A. K., Shim, Y. M., Hochreiter, A. E., Borish, L., & Ravichandran, K. S. (2012) · Nature · doi:10.1038/nature11714 · Cited by 287 · see citing works

Phosphatidylserine receptor BAI1 and apoptotic cells as new promoters of myoblast fusion

Hochreiter, A. E., Lee, C. S., Kinchen, J. M., Sokolowski, J. D., Arandjelovic, S., Call, J. A., Klibanov, A. L., Yan, Z., Mandell, J. W., & Ravichandran, K. S. (2013) · Nature · doi:10.1038/nature12135 · Cited by 286 · see citing works

Two pathways converge at CED-10 to mediate actin rearrangement and corpse removal in C. elegans

Kinchen, J. M., Cabello, J., Klingele, D., Wong, K., Feichtinger, R., Schnabel, H., Schnabel, R., & Hengartner, M. O. (2005) · Nature · doi:10.1038/nature03263 · Cited by 266 · see citing works

ATP-Binding Cassette Transporters, Atherosclerosis, and Inflammation

Westerterp, M., Bochem, A. E., Yvan‐Charvet, L., Murphy, A. J., Wang, N., & Tall, A. R. (2014) · Circulation Research · doi:10.1161/circresaha.114.300738 · Cited by 257 · see citing works

Promoter-Specific Roles for Liver X Receptor/Corepressor Complexes in the Regulation of ABCA1 and SREBP1 Gene Expression

Wagner, B. L., Valledor, A. F., Shao, G. Q., Daige, C. L., Bischoff, E. D., Petrowski, M. L., Jepsen, K., Baek, S. H., Heyman, R. A., Rosenfeld, M. G., et al. (2003) · Molecular and Cellular Biology · doi:10.1128/mcb.23.16.5780-5789.2003 · Cited by 245 · see citing works

T and B cell hyperactivity and autoimmunity associated with niche-specific defects in apoptotic body clearance in TIM-4-deficient mice

Rodriguez‐Manzanet, R., Sanjuán, M. A. F., Wu, H. Y., Quintana, F. J., Xiao, S., Anderson, A. C., Weiner, H. L., Green, D. R., & Kuchroo, V. K. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0910359107 · Cited by 182 · see citing works

Unexpected requirement for ELMO1 in clearance of apoptotic germ cells in vivo

Elliott, M. R., Zheng, S., Park, D., Woodson, R. I., Reardon, M. A., Juncadella, I. J., Kinchen, J. M., Zhang, J., Lysiak, J. J., & Ravichandran, K. S. (2010) · Nature · doi:10.1038/nature09356 · Cited by 175 · see citing works

The Phosphatidylserine Receptor TIM-4 Does Not Mediate Direct Signaling

Park, D., Hochreiter, A. E., & Ravichandran, K. S. (2009) · Current Biology · doi:10.1016/j.cub.2009.01.042 · Cited by 158 · see citing works

Activation of LXRs prevents bile acid toxicity and cholestasis in female mice

Uppal, H., Saini, S. P. S., Moschetta, A., Mu, Y., Zhou, J., Gong, H., Zhai, Y., Ren, S., Michalopoulos, G. K., Mangelsdorf, D. J., et al. (2007) · Hepatology · doi:10.1002/hep.21494 · Cited by 149 · see citing works

The involvement of the monocytes/macrophages in chronic inflammation associated with atherosclerosis

Fenyo, I. M., & Gafencu, A. V. (2013) · Immunobiology · doi:10.1016/j.imbio.2013.06.005 · Cited by 144 · 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

Variations on a Gene: Rare and Common Variants in ABCA1 and Their Impact on HDL Cholesterol Levels and Atherosclerosis

Brunham, L. R., Singaraja, R. R., & Hayden, M. R. (2006) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.26.061505.111214 · Cited by 142 · see citing works

Transglutaminase 2 Is Needed for the Formation of an Efficient Phagocyte Portal in Macrophages Engulfing Apoptotic Cells

Tóth, B. B., Garabuczi, É., Sarang, Z., Vereb, G., Vámosi, G., Aeschlimann, D. P., Blaskó, B., Bécsi, B., Erdődi, F., Lacy‐Hulbert, A., et al. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0803444 · Cited by 137 · see citing works

Regulation of macrophage function in inflammation and atherosclerosis

Shibata, N., & Glass, C. K. (2008) · Journal of Lipid Research · doi:10.1194/jlr.r800063-jlr200 · Cited by 124 · 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

Illuminating HDL — Is It Still a Viable Therapeutic Target?

Rader, D. J. (2007) · New England Journal of Medicine · doi:10.1056/nejme0707210 · Cited by 119 · see citing works

Regulation of reverse cholesterol transport - a comprehensive appraisal of available animal studies

Annema, W., & Tietge, U. (2012) · Nutrition and Metabolism · doi:10.1186/1743-7075-9-25 · Cited by 108 · see citing works

The role of macrophages and dendritic cells in the clearance of apoptotic cells in advanced atherosclerosis

Thorp, E., Subramanian, M., & Tabas, I. (2011) · European Journal of Immunology · doi:10.1002/eji.201141719 · Cited by 107 · see citing works

Molecular basis of cholesterol homeostasis: lessons from Tangier disease and ABCA1

Oram, J. F. (2002) · Trends in Molecular Medicine · doi:10.1016/s1471-4914(02)02289-x · Cited by 104 · see citing works

Microenvironmental influences of apoptosis in vivo and in vitro

Gregory, C. D., & Pound, J. D. (2010) · APOPTOSIS · doi:10.1007/s10495-010-0485-9 · Cited by 101 · see citing works

Discovery of Tertiary Sulfonamides as Potent Liver X Receptor Antagonists

Zuercher, W. J., Buckholz, R. G., Campobasso, N., Collins, J. L., Galardi, C. M., Gampe, R. T., Hyatt, S. M., Merrihew, S., Moore, J. T., Oplinger, J. A., et al. (2010) · Journal of Medicinal Chemistry · doi:10.1021/jm901797p · Cited by 97 · see citing works

In Vivo Reverse Cholesterol Transport From Macrophages Lacking ABCA1 Expression Is Impaired

Wang, M., Franklin, V., & Marcel, Y. L. (2007) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.107.146068 · Cited by 78 · see citing works

Myeloid cells in atherosclerosis

Koltsova, E. K., Hedrick, C. C., & Ley, K. F. (2013) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e328363d298 · Cited by 67 · see citing works

Endothelial expression of human ABCA1 in mice increases plasma HDL cholesterol and reduces diet-induced atherosclerosis

Vaisman, B. L., Demosky, S. J., Stonik, J. A., Ghias, M., Knapper, C., Sampson, M. L., Dai, C., Levine, S. J., & Remaley, A. T. (2011) · Journal of Lipid Research · doi:10.1194/jlr.m018713 · Cited by 55 · see citing works

Dancing with the sterols: Critical roles for ABCG1, ABCA1, miRNAs, and nuclear and cell surface receptors in controlling cellular sterol homeostasis

Tarling, E. J., & Edwards, P. A. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2011.07.011 · Cited by 54 · see citing works

Current concept of reverse cholesterol transport and novel strategy for atheroprotection.

Ono, K. (2012) · Journal of Cardiology · doi:10.1016/j.jjcc.2012.07.014 · Cited by 51 · see citing works

Cellular Regulation of the Inflammatory Response

Janssen, W. J., & Henson, P. M. (2011) · Toxicologic Pathology · doi:10.1177/0192623311428477 · Cited by 50 · see citing works

Identification and Characterization of a Dimerization Domain in CED-6, an Adapter Protein Involved in Engulfment of Apoptotic Cells

Su, H.-P., Brugnera, E., Criekinge, W. V., Smits, E., Hengartner, M. O., Bogaert, T., & Ravichandran, K. S. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.13.9542 · Cited by 49 · see citing works

Regulation of cholesterol efflux from macrophages

Marcel, Y. L., Ouimet, M. I., & Wang, M. (2008) · Current Opinion in Lipidology · doi:10.1097/mol.0b013e32830f4a1d · Cited by 45 · see citing works

Nuclear Receptors and Clearance of Apoptotic Cells: Stimulating the Macrophage’s Appetite

A-González, N., & Hidalgo, A. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00211 · Cited by 34 · see citing works

Myeloid Cell–Specific ATP-Binding Cassette Transporter A1 Deletion Has Minimal Impact on Atherogenesis in Atherogenic Diet–Fed Low-Density Lipoprotein Receptor Knockout Mice

Bi, X., Zhu, X., Gao, C., Shewale, S. V., Cao, Q., Liu, M., Boudyguina, E. Y., Gebre, A. K., Wilson, M. D., Brown, A. L., et al. (2014) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.114.303791 · Cited by 31 · see citing works

Participation of Innate and Acquired Immunity in Atherosclerosis

Curtiss, L. K., Kubo, N., Schiller, N. K., & Boisvert, W. A. (2000) · Immunologic Research · doi:10.1385/ir:21:2-3:167 · Cited by 28 · see citing works

ATP-binding cassette transporter A1: key player in cardiovascular and metabolic disease at local and systemic level

van Eck, M. (2014) · Current Opinion in Lipidology · doi:10.1097/mol.0000000000000088 · Cited by 25 · see citing works

Effects of Deletion of Macrophage ABCA7 on Lipid Metabolism and the Development of Atherosclerosis in the Presence and Absence of ABCA1

Meurs, I., Calpe‐Berdiel, L., Habets, K. L. L., Zhao, Y., Korporaal, S. J. A., Mommaas, A. M., Josselin, E., Hildebrand, R. B., Ye, D., Out, R., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0030984 · Cited by 24 · see citing works

High Density Lipoproteins Put Out the Fire

Moore, K., & Fisher, E. (2014) · Cell Metabolism · doi:10.1016/j.cmet.2014.01.009 · Cited by 12 · see citing works

Recognition of apoptotic cells by viable cells is specific, ubiquitous, and species independent: analysis using photonic crystal biosensors

Pattabiraman, G., Lidstone, E. A., Palasiewicz, K., Cunningham, B. T., & Ucker, D. S. (2014) · Molecular Biology of the Cell · doi:10.1091/mbc.e13-11-0700 · Cited by 9 · see citing works

Efferocytosis in health and disease

Doran, A. C., Yurdagul, A., & Tabas, I. (2020) · Nature Reviews Immunology · doi:10.1038/s41577-019-0240-6 · Cited by 1,066 · 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

Phagocytosis: An Immunobiologic Process

Gordon, S. (2016) · Immunity · doi:10.1016/j.immuni.2016.02.026 · Cited by 902 · see citing works

The clearance of dead cells by efferocytosis

Boada-Romero, E., Martinez, J., Heckmann, B. L., & Green, D. R. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-0232-1 · Cited by 893 · see citing works

Macrophage Metabolism of Apoptotic Cell-Derived Arginine Promotes Continual Efferocytosis and Resolution of Injury

Yurdagul, A., Subramanian, M., Wang, X., Crown, S. B., Ilkayeva, O. R., Darville, L., Kolluru, G. K., Rymond, C. C., Gerlach, B. D., Zheng, Z., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2020.01.001 · Cited by 525 · see citing works

Drugging the efferocytosis process: concepts and opportunities

Mehrotra, P., & Ravichandran, K. S. (2022) · Nature Reviews Drug Discovery · doi:10.1038/s41573-022-00470-y · Cited by 459 · see citing works

Efferocytosis 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

Living on the Edge: Efferocytosis at the Interface of Homeostasis and Pathology

Morioka, S., Maueröder, C., & Ravichandran, K. S. (2019) · Immunity · doi:10.1016/j.immuni.2019.04.018 · Cited by 391 · 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

Intracellular and Intercellular Aspects of Macrophage Immunometabolism in Atherosclerosis

Tabas, I. A., & Bornfeldt, K. (2020) · Circulation Research · doi:10.1161/circresaha.119.315939 · Cited by 249 · see citing works

Liver X receptors link lipid metabolism and inflammation

Schulman, I. G. (2017) · FEBS Letters · doi:10.1002/1873-3468.12702 · Cited by 244 · see citing works

Apoptotic cell recognition receptors and scavenger receptors

Penberthy, K. K., & Ravichandran, K. S. (2015) · Immunological Reviews · doi:10.1111/imr.12376 · Cited by 202 · see citing works

Dendritic cell maturation in cancer

Moon, C. Y., Belabed, M., Park, M. D., Mattiuz, R., Puleston, D. J., & Mérad, M. (2025) · Nature reviews. Cancer · doi:10.1038/s41568-024-00787-3 · Cited by 186 · see citing works

Liver X Receptors: Regulators of Cholesterol Metabolism, Inflammation, Autoimmunity, and Cancer

Bilotta, M. T., Petillo, S., Santoni, A., & Cippitelli, M. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.584303 · Cited by 174 · see citing works

Efferocytosis in atherosclerosis

Adkar, S. S., & Leeper, N. J. (2024) · Nature Reviews Cardiology · doi:10.1038/s41569-024-01037-7 · Cited by 166 · 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

Extracellular vesicles arising from apoptosis: forms, functions, and applications

Gregory, C. D., & Rimmer, M. P. (2023) · The Journal of Pathology · doi:10.1002/path.6138 · Cited by 140 · see citing works

Granulopoiesis and Neutrophil Homeostasis: A Metabolic, Daily Balancing Act

Yvan‐Charvet, L., & Ng, L. G. (2019) · Trends in Immunology · doi:10.1016/j.it.2019.05.004 · Cited by 130 · see citing works

Deficiency of ATP-Binding Cassette Transporters A1 and G1 in Endothelial Cells Accelerates Atherosclerosis in Mice

Westerterp, M., Tsuchiya, K., Tattersall, I. W., Fotakis, P., Bochem, A. E., Molusky, M. M., Ntonga, V., Abramowicz, S., Parks, J. S., Welch, C. L., et al. (2016) · Arteriosclerosis, Thrombosis, and Vascular Biology · doi:10.1161/atvbaha.115.306670 · Cited by 114 · see citing works

The Phagocytic Code Regulating Phagocytosis of Mammalian Cells

Cockram, T. O. J., Dundee, J. M., Popescu, A. S., & Brown, G. C. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.629979 · Cited by 111 · see citing works

LXR signaling controls homeostatic dendritic cell maturation

Bosteels, V., Maréchal, S., Nolf, C. D., Rennen, S., Maelfait, J., Tavernier, S. J., Vetters, J., Velde, E. V. D., Fayazpour, F., Deswarte, K., et al. (2023) · Science Immunology · doi:10.1126/sciimmunol.add3955 · Cited by 111 · see citing works

Interpreting an apoptotic corpse as anti-inflammatory involves a chloride sensing pathway

Perry, J. S. A., Morioka, S., Medina, C. B., Etchegaray, J. I., Barron, B. J., Raymond, M. H., Lucas, C. D., Önengüt-Gümüşcü, S., Delpire, E. J., & Ravichandran, K. S. (2019) · Nature Cell Biology · doi:10.1038/s41556-019-0431-1 · Cited by 105 · see citing works

First we eat, then we do everything else: The dynamic metabolic regulation of efferocytosis

Trzeciak, A. J., Wang, Y., & Perry, J. S. A. (2021) · Cell Metabolism · doi:10.1016/j.cmet.2021.08.001 · Cited by 107 · see citing works

Clearance of Dying Cells by Phagocytes: Mechanisms and Implications for Disease Pathogenesis

Fond, A. M., & Ravichandran, K. S. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-39406-0_2 · Cited by 92 · see citing works

Effect of high fat diet on phenotype, brain transcriptome and lipidome in Alzheimer’s model mice

Nam, K. N., Mounier, A., Wolfe, C. M., Fitz, N. F., Carter, A. Y., Castranio, E. L., Kamboh, H., Reeves, V. L., Wang, J., Han, X., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-04412-2 · Cited by 94 · see citing works

Targeting Efferocytosis in Inflammaging

Poon, I. K. H., & Ravichandran, K. S. (2023) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev-pharmtox-032723-110507 · Cited by 92 · see citing works

Cellular Responses to the Efferocytosis of Apoptotic Cells

Yin, C., & Heit, B. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.631714 · Cited by 92 · 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

Polyamine import and accumulation causes immunomodulation in macrophages engulfing apoptotic cells

McCubbrey, A. L., McManus, S. A., McClendon, J. D., Thomas, S. M., Chatwin, H. B., Reisz, J. A., D’Alessandro, A., Mould, K. J., Bratton, D. L., Henson, P. M., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2021.110222 · Cited by 81 · see citing works

Luteolin Attenuates Foam Cell Formation and Apoptosis in Ox-LDL-Stimulated Macrophages by Enhancing Autophagy

Zhang, B., Zhang, C.-W., Wang, C., Pan, D.-F., Xu, T.-D., & Li, D.-Y. (2016) · Cellular Physiology and Biochemistry · doi:10.1159/000447902 · Cited by 80 · see citing works

Transcriptional control of apoptotic cell clearance by macrophage nuclear receptors

Rőszer, T. (2016) · APOPTOSIS · doi:10.1007/s10495-016-1310-x · Cited by 80 · 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

The ABCA1-efferocytosis axis: A new strategy to protect against atherosclerosis

Chen, W., Li, L., Wang, J., Zhang, R., Zhang, T., Wu, Y., Wang, S., & Xing, D. (2021) · Clinica Chimica Acta · doi:10.1016/j.cca.2021.02.025 · Cited by 84 · see citing works

After cell death: the molecular machinery of efferocytosis

Moon, B., Yang, S., Moon, H., Lee, J., & Park, D. (2023) · Experimental & Molecular Medicine · doi:10.1038/s12276-023-01070-5 · Cited by 78 · see citing works

Cholesterol 25-hydroxylase promotes efferocytosis and resolution of lung inflammation

Madenspacher, J. H., Morrell, E. D., Gowdy, K. M., McDonald, J. G., Thompson, B. M., Muse, G. W., Martinez, J., Thomas, S. Y., Mikacenic, C. R., Nick, J. A., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.137189 · Cited by 73 · see citing works

Regulation of ATP binding cassette transporter A1 (ABCA1) expression: cholesterol-dependent and – independent signaling pathways with relevance to inflammatory lung disease

He, P., Gelissen, I. C., & Ammit, A. J. (2020) · Respiratory Research · doi:10.1186/s12931-020-01515-9 · Cited by 70 · see citing works

Dysregulated cellular metabolism in atherosclerosis: mediators and therapeutic opportunities

Stroope, C., Nettersheim, F. S., Coon, B. G., Finney, A. C., Schwartz, M. A., Ley, K. F., Rom, O., & Yurdagul, A. (2024) · Nature Metabolism · doi:10.1038/s42255-024-01015-w · Cited by 72 · see citing works

Eating the dead to keep atherosclerosis at bay

Brophy, M. L., Dong, Y., Wu, H., Rahman, H. N. A., Song, K., & Chen, H. (2017) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2017.00002 · Cited by 68 · see citing works

The adhesion GPCR BAI1 mediates macrophage ROS production and microbicidal activity against Gram-negative bacteria

Billings, E. A., Lee, C. S., Owen, K. A., D’Souza, R. S., Ravichandran, K. S., & Casanova, J. E. (2016) · Science Signaling · doi:10.1126/scisignal.aac6250 · Cited by 68 · see citing works

Adhesion GPCRs in Regulating Immune Responses and Inflammation

Lin, H., Hsiao, C., Pabst, C., Hébert, J., Schöneberg, T., & Hamann, J. (2017) · Advances in immunology · doi:10.1016/bs.ai.2017.05.005 · Cited by 67 · see citing works

Adiponectin and Adiponectin Receptors in Atherosclerosis

Gianopoulos, I., Mantzoros, C. S., & Daskalopoulou, S. S. (2024) · Endocrine Reviews · doi:10.1210/endrev/bnae021 · Cited by 71 · see citing works

Regulation of Apoptotic Cell Clearance During Resolution of Inflammation

Arienti, S., Barth, N. D., Dorward, D. A., Rossi, A. G., & Dransfield, I. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00891 · Cited by 64 · see citing works

MicroRNA regulation of macrophages in human pathologies

Wei, Y., & Schober, A. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-016-2254-6 · Cited by 63 · see citing works

Clearance of Apoptotic Cells by Tissue Epithelia: A Putative Role for Hepatocytes in Liver Efferocytosis

Davies, S. P., Reynolds, G. M., & Stamataki, Z. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00044 · Cited by 61 · see citing works

ATP binding cassette A1 (ABCA1) mediates microparticle formation during high-density lipoprotein (HDL) biogenesis

Hafiane, A., & Genest, J. J. (2017) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2017.01.013 · Cited by 57 · see citing works

Rethinking Phagocytes: Clues from the Retina and Testes

Penberthy, K. K., Lysiak, J. J., & Ravichandran, K. S. (2018) · Trends in Cell Biology · doi:10.1016/j.tcb.2018.01.004 · Cited by 57 · see citing works

Immunomodulation of wound healing leading to efferocytosis

Zhao, Y., Li, M., Mao, J., Su, Y., Huang, X., Xia, W., Leng, X., & Zan, T. (2024) · Smart Medicine · doi:10.1002/smmd.20230036 · Cited by 52 · see citing works

Adhesion GPCRs as Modulators of Immune Cell Function

Hamann, J., Hsiao, C., Lee, C. S., Ravichandran, K. S., & Lin, H. (2016) · Handbook of experimental pharmacology · doi:10.1007/978-3-319-41523-9_15 · Cited by 52 · see citing works

Efferocytosis by macrophages in physiological and pathological conditions: regulatory pathways and molecular mechanisms

Sheng, Y.-R., Hu, W.-T., Chen, S.-M., & Zhu, X.-Y. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1275203 · Cited by 41 · see citing works

Microenvironmental Effects of Cell Death in Malignant Disease

Gregory, C. D., Ford, C. A., & Voss, J. J. L. P. (2016) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-39406-0_3 · Cited by 41 · see citing works

A Novel Function for 15-Lipoxygenases in Cholesterol Homeostasis and CCL17 Production in Human Macrophages

Snodgrass, R. G., Zezina, E. A., Namgaladze, D., Gupta, S., Angioni, C., Geißlinger, G., Lütjohann, D., & Brüne, B. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01906 · Cited by 42 · see citing works

Identification of direct target genes of miR-7, miR-9, miR-96, and miR-182 in the human breast cancer cell lines MCF-7 and MDA-MB-231

Moazzeni, H., Najafi, A., & Khani, M. (2017) · Molecular and Cellular Probes · doi:10.1016/j.mcp.2017.05.005 · Cited by 41 · see citing works

Tumour‐associated macrophage‐derived DOCK7‐enriched extracellular vesicles drive tumour metastasis in colorectal cancer via the RAC1/ABCA1 axis

Chen, W. T., Zhou, M., Guan, B., Xie, B., Liu, Y., He, J., Zhao, J., Zhao, Q., & Yan, D. (2024) · Clinical and Translational Medicine · doi:10.1002/ctm2.1591 · Cited by 40 · see citing works

Apoptotic cell induction of miR-10b in macrophages contributes to advanced atherosclerosis progression in ApoE−/− mice

Wang, D.-L., Wang, W.-T., Lin, W.-Q., Yang, W., Zhang, P., Chen, M., Ding, D., Liu, C.-Q., Zheng, J., & Ling, W. (2018) · Cardiovascular Research · doi:10.1093/cvr/cvy132 · Cited by 33 · see citing works

Phosphatidylserine in atherosclerosis

Darabi, M., & Kontush, A. (2016) · Current Opinion in Lipidology · doi:10.1097/mol.0000000000000298 · Cited by 38 · see citing works

Phosphatidylserine enhances anti‐inflammatory effects of reconstituted HDL in macrophages via distinct intracellular pathways

Darabi, M., Lhomme, M., Dahik, V. D., Guillas, I., Frisdal, É., Tubeuf, E., Poupel, L., Patel, M., Gautier, E. L., Huby, T., et al. (2022) · The FASEB Journal · doi:10.1096/fj.201800810r · Cited by 32 · see citing works

Pharmacological mechanisms by which baicalin ameliorates cardiovascular disease

Si, L., & Lai, Y. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1415971 · Cited by 34 · see citing works

Context-dependent compensation among phosphatidylserine-recognition receptors

Penberthy, K. K., Rival, C., Shankman, L. S., Raymond, M. H., Zhang, J., Perry, J. S. A., Lee, C. S., Han, C. Z., Onengut-Gumuscu, S., Palczewski, K., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-15191-1 · Cited by 30 · see citing works

Hijacking homeostasis: Regulation of the tumor microenvironment by apoptosis

Gregory, C. D. (2023) · Immunological Reviews · doi:10.1111/imr.13259 · Cited by 28 · see citing works

Silencing SGK1 alleviates osteoarthritis through epigenetic regulation of CREB1 and ABCA1 expression

Wang, Z., Ni, S., Zhang, H., Fan, Y., Xia, L., & Li, N. (2020) · Life Sciences · doi:10.1016/j.lfs.2020.118733 · Cited by 27 · see citing works

Participation of ABCA1 Transporter in Pathogenesis of Chronic Obstructive Pulmonary Disease

Kotlyarov, S. N. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22073334 · Cited by 27 · see citing works

Microneedle delivery of CAR-M-like engineered macrophages alleviates intervertebral disc degeneration through enhanced efferocytosis capacity

Zhou, X., Zhu, D., Wu, D., Li, G., Liang, H., Zhang, W., Wu, Y., Xu, H., Zhang, Z., Tong, B., et al. (2025) · Cell Reports Medicine · doi:10.1016/j.xcrm.2025.102079 · Cited by 26 · see citing works

Sensing of apoptotic cells through Axl causes lung basal cell proliferation in inflammatory diseases

Fujino, N., Brand, O. J., Morgan, D. J., Fujimori, T., Grabiec, A. M., Jagger, C. P., Maciewicz, R. A., Yamada, M., Itakura, K., Sugiura, H., et al. (2019) · The Journal of Experimental Medicine · doi:10.1084/jem.20171978 · Cited by 25 · see citing works

Effect of nitroprusside on arteriolar constriction after retinal branch vein occlusion.

Donati, G., Pournaras, C. J., & Tsacopoulos, M. (1998) · PubMed · Cited by 26 · see citing works

Phytochemical-mediated efferocytosis and autophagy in inflammation control

Vafadar, A., Tajbakhsh, A., Hosseinpour-Soleimani, F., Savardshtaki, A., & Hashempur, M. H. (2024) · Cell Death Discovery · doi:10.1038/s41420-024-02254-2 · Cited by 27 · see citing works

Having an Old Friend for Dinner: The Interplay between Apoptotic Cells and Efferocytes

Lam, A. L., & Heit, B. (2021) · Cells · doi:10.3390/cells10051265 · Cited by 22 · see citing works

Cellular mechanisms underlying the impairment of macrophage efferocytosis

Ma, Y., Kemp, S. S., Yang, X., Wu, M. H., & Yuan, S. Y. (2023) · Immunology Letters · doi:10.1016/j.imlet.2023.02.001 · Cited by 22 · see citing works

Immunometabolism in atherosclerotic disorders

Fleetwood, A. J., Noonan, J. E., Gruta, N. L. L., Kallies, A., & Murphy, A. J. (2024) · Nature Cardiovascular Research · doi:10.1038/s44161-024-00473-5 · Cited by 22 · see citing works

Understanding the Role of the BAI Subfamily of Adhesion G Protein-Coupled Receptors (GPCRs) in Pathological and Physiological Conditions

Moon, S. Y., Shin, S.-A., Oh, Y., Park, H. H., & Lee, C. S. (2018) · Genes · doi:10.3390/genes9120597 · Cited by 21 · see citing works

Regulatory roles of brain-specific angiogenesis inhibitor 1(BAI1) protein in inflammation, tumorigenesis and phagocytosis: A brief review

Mathema, V. B., & Na‐Bangchang, K. (2017) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2017.01.006 · Cited by 22 · see citing works

Lipid metabolism as a mechanism of immunomodulation in macrophages: the role of liver X receptors

Leußink, S., Aranda-Pardos, I., & A-González, N. (2020) · Current Opinion in Pharmacology · doi:10.1016/j.coph.2020.02.003 · Cited by 21 · see citing works

Apoptotic cells trigger the ABCA1/STAT6 pathway leading to PPAR-γ expression and activation in macrophages

Kim, M.-J., Lee, Y.-J., Yoon, Y.-S., Kim, M., Choi, J. H., Kim, H.-S., & Kang, J. L. (2018) · Journal of Leukocyte Biology · doi:10.1002/jlb.2a0817-341rr · Cited by 21 · see citing works

What’s the deal with efferocytosis and asthma?

Martinez, J., & Cook, D. N. (2021) · Trends in Immunology · doi:10.1016/j.it.2021.08.004 · Cited by 19 · see citing works

Role of Adhesion G Protein-Coupled Receptors in Immune Dysfunction and Disorder

Tseng, W.-Y., Stacey, M. A., & Lin, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24065499 · Cited by 19 · see citing works

Metabolic reprogramming in efferocytosis

Yan, Q., Li, K., Chen, L., Wang, A., Xi, Y., Xiao, H., & Yuan, L. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1677028 · Cited by 18 · see citing works

Components of the Engulfment Machinery Have Distinct Roles in Corpse Processing

Meehan, T. L., Joudi, T. F., Timmons, A. K., Taylor, J. D., Habib, C. S., Peterson, J. S., Emmanuel, S. N., Franc, N. C., & McCall, K. (2016) · PLoS ONE · doi:10.1371/journal.pone.0158217 · Cited by 18 · see citing works

Ghost messages: cell death signals spread

Zhang, M., Lin, Y., Chen, R., Yu, H., Li, Y., Chen, M., Dou, C., Yin, P., Zhang, L., & Tang, P. (2023) · Cell Communication and Signaling · doi:10.1186/s12964-022-01004-0 · Cited by 18 · see citing works

Age-dependent differences in efferocytosis determine the outcome of opsonophagocytic protection from invasive pathogens

Bee, G. C. W., Lokken-Toyli, K. L., Yeung, S. T., Rodriguez, L., Zangari, T., Anderson, E. E., Ghosh, S., Rothlin, C. V., Brodin, P., Khanna, K. M., et al. (2023) · Immunity · doi:10.1016/j.immuni.2023.03.018 · Cited by 17 · see citing works

ELMO1 ameliorates intestinal epithelial cellular senescence via SIRT1/p65 signaling in inflammatory bowel disease-related fibrosis

Chen, J., Li, G., He, X., Chen, Z., Chen, Z., Liu, D., Guo, S., Huang, T., Lan, P., Lan, P., et al. (2023) · Gastroenterology report · doi:10.1093/gastro/goae045 · Cited by 16 · see citing works

7-Ketocholesterol and cholestane-triol increase expression of SMO and LXRα signaling pathways in a human breast cancer cell line

Levy, D., de Melo, T. C., Oliveira, B. A., Paz, J. L., de Freitas, F. A., Reichert, C. O., Rodrigues, A., & Bydlowski, S. P. (2018) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2018.12.008 · Cited by 14 · see citing works

Bridging molecules are secreted from the skeletal muscle and potentially regulate muscle differentiation

Chikazawa, M., Shimizu, M., Yamauchi, Y., & Sato, R. (2019) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2019.11.010 · Cited by 13 · see citing works

Cytoskeletal orchestration of glucose uptake in Sertoli cell to support efferocytosis of apoptotic germ cells

Wu, D., Pandupuspitasari, N. S., Zhang, K., Tang, Y., Khan, F. A., Li, H., Huang, C., & Sun, F. (2023) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2023.119434 · Cited by 13 · see citing works

ABCA1 affects placental function via trophoblast and macrophage

Xie, C., Lin, L., Long, Y., Yang, J., Xiaoju, W., Xiaohui, C., & Huimin, G. (2017) · Life Sciences · doi:10.1016/j.lfs.2017.10.031 · Cited by 13 · see citing works

Reinterpretation of the localization of the ATP binding cassette transporter ABCG1 in insulin-secreting cells and insights regarding its trafficking and function

Harris, M. T., Hussain, S. S., Inouye, C. M., Castle, A. M., & Castle, J. D. (2018) · PLoS ONE · doi:10.1371/journal.pone.0198383 · Cited by 11 · see citing works

Macrophage immunometabolism in diabetes-associated atherosclerosis

dos Santos, B. G., & Goedeke, L. (2023) · Immunometabolism · doi:10.1097/in9.0000000000000032 · Cited by 9 · see citing works

The Impaired Mechanism and Facilitated Therapies of Efferocytosis in Atherosclerosis

Wang, Z., Su, J. Y., Gong, F., Xue, L., & Su, Z. (2022) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000001311 · Cited by 10 · see citing works

Luteolin Nanomedicine with Stimulus-Driven Traceless Release for Targeting Treatment of Atherosclerosis by Enhancing Lipid Efflux

Chen, S., Wang, Z., Shen, Z., He, D., Liu, L., Qian, L.-B., Ma, B., & Huang, H. (2025) · Research · doi:10.34133/research.0754 · Cited by 9 · see citing works

After-Death Functions of Cell Death.

Lee, Y., & Overholtzer, M. (2019) · Europe PMC (PubMed Central) · Cited by 9 · see citing works

Cholesterol efflux protein, ABCA1, supports anticancer functions of myeloid immune cells

Bendre, S. V., Wang, Y., Hajyousif, B., K C, R., Bhogale, S. G., Pradeep, D., Krawczynska, N., Schane, C. P., Weisser, E., Singh, A., et al. (2026) · Science Advances · doi:10.1126/sciadv.adx5490 · Cited by 8 · see citing works

Dipotassium glycyrrhizate and hinokitiol enhance macrophage efferocytosis by regulating recognition, uptake, and metabolism of apoptotic cells in vitro

Yamamoto, Y., Yamaguchi, T., Egashira, K., 才木脩平, Kimura, M., Chikazawa, T., Yamamoto, Y., & Kurita, K. (2023) · Journal of Periodontal Research · doi:10.1111/jre.13228 · Cited by 8 · see citing works

More Than a Cleanup Crew: The Expanding Biology of Efferocytosis

Pandit, R., Hillman, H., Williams, J. W., & Yurdagul, A. (2025) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.125.323211 · Cited by 7 · see citing works

Liver X receptors conserve the therapeutic target potential for the treatment of rheumatoid arthritis

Mai, C.-T., Zheng, D.-C., Li, X., Zhou, H., & Xie, Y. (2021) · Pharmacological Research · doi:10.1016/j.phrs.2021.105747 · Cited by 8 · see citing works

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 · see citing works

Enhancement of Anti-inflammatory Effects of Synthetic High-Density Lipoproteins by Incorporation of Anionic Lipids

Yu, M., Hong, K. W., Halseth, T. A., & Schwendeman, A. A. (2023) · Molecular Pharmaceutics · doi:10.1021/acs.molpharmaceut.3c00175 · Cited by 6 · see citing works

Efferocytosis deficiency exacerbates local inflammation and predicts recurrence in chronic rhinosinusitis with nasal polyps

Liang, S., Cao, B. Y., Shen, S., Li, Y., Zhang, L., & Wang, C. (2026) · Journal of Allergy and Clinical Immunology · doi:10.1016/j.jaci.2025.12.1016 · Cited by 7 · see citing works

The Liver X Receptor Promotes Immune Homeostasis via Controlled Activation of the Innate Immune System in the Liver

Nakashima, H., Kearney, B. M., & Kinoshita, M. (2024) · Biomolecules · doi:10.3390/biom15010025 · Cited by 6 · see citing works

Apoptosis and Efferocytosis in Inflammatory Diseases

Purnama, C. A., Meiliana, A., Barliana, M. I., Dandan, K. L., & Wijaya, A. (2021) · The Indonesian Biomedical Journal · doi:10.18585/inabj.v13i3.1608 · Cited by 5 · see citing works

Hypoxic stress caused apoptosis of MDBK cells by p53/BCL6-mitochondrial apoptosis pathway

Li, B., Baima, Y.-J., De, J., Wen, D., Liu, Y., Zhuzha, B., & Jiang, N. (2024) · Animal Biotechnology · doi:10.1080/10495398.2023.2299241 · Cited by 4 · see citing works

Dysregulation of the engulfment pathway in the gut fuels Inflammatory Bowel DiseasePreprint

Suarez, K., Lim, E., Singh, S., Pereira, M. P., Joosen, L., Ibeawuchi, S., Dunkel, Y., Mittal, Y., Ho, S. B., Chattopadhyay, R., et al. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/280172 · Cited by 4 · see citing works

Modulation of immune cells and metabolic reprogramming in efferocytosis

Oliveira, K. C., Marcos, C., Penteado, L. D. A., Dejani, N., Moraes-Vieira, P., & Medeiros, A. (2026) · Cell Death and Disease · doi:10.1038/s41419-026-08431-8 · Cited by 4 · see citing works

Regulation of ABCA1 Expression During Apoptotic Cell Engulfment

Fond, A. (2015) · doi:10.18130/v3027n

ABCA1 and ABCG1 Protect Against Oxidative Stress–Induced Macrophage Apoptosis During Efferocytosis

Yvan-Charvet, L., Pagler, T. A., Seimon, T. A., Thorp, E., Welch, C. L., Witztum, J. L., Tabas, I., & Tall, A. R. (2010) · Circulation Research · doi:10.1161/circresaha.110.217281 · Cited by 217 · 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

Functional ABCG1 expression induces apoptosis in macrophages and other cell types

Seres, L., Cserepes, J., Elkind, N. B., Törőcsik, D., Nagy, L., Sarkadi, B., & Homolya, L. (2008) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2008.06.010 · Cited by 35 · see citing works

ABCA1 Is the cAMP-inducible Apolipoprotein Receptor That Mediates Cholesterol Secretion from Macrophages

Oram, J. F., Lawn, R. M., Garvin, M. R., & Wade, D. P. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.m006738200 · Cited by 537 · see citing works