Efferocytosis induces macrophage proliferation to help resolve tissue injury
Open accessAbstract
Apoptotic cell clearance by macrophages (efferocytosis) promotes resolution signaling pathways, which can be triggered by molecules derived from the phagolysosomal degradation of apoptotic cells. We show here that nucleotides derived from the hydrolysis of apoptotic cell DNA by phagolysosomal DNase2a activate a DNA-PKcs-mTORC2/Rictor pathway that increases Myc to promote non-inflammatory macrophage proliferation. Efferocytosis-induced proliferation expands the pool of resolving macrophages in vitro and in mice, including zymosan-induced peritonitis, dexamethasone-induced thymocyte apoptosis, and atherosclerosis regression. In the dexamethasone-thymus model, hematopoietic Rictor deletion blocked efferocytosing macrophage proliferation, apoptotic cell clearance, and tissue resolution. In atherosclerosis regression, silencing macrophage Rictor or DNase2a blocked efferocyte proliferation, apoptotic cell clearance, and plaque stabilization. In view of previous work showing that other types of apoptotic cell cargo can promote resolution in individual efferocytosing macrophages, the findings here suggest that signaling-triggered apoptotic cell-derived nucleotides can amplify this benefit by increasing the number of these macrophages.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
EIMP expands the pool of reparative macrophages, enhancing their capacity for continual apoptotic cell clearance and tissue resolution, and may underlie the sustained reparative capacity of MerTK+ macrophages.
“This expands the pool of reparative macrophages, enhancing their capacity for continual apoptotic cell clearance and tissue resolution, and may underlie the sustained reparative capacity exhibited by MerTK+ macrophages (46).”
From Macrophage duality in liver diseases: heterogeneity, plasticity, and the quest for precision therapeutics (2026) · cites this paper as [46]
The Discussion (page unavailable) says EIMP expands a pool of macrophages competent at continual efferocytosis and pro-resolving activity, and links that expansion to improved apoptotic-cell clearance and resolution. The Results (page unavailable) identify MerTK signaling as one contributor to EIMP, but the paper does not establish sustained reparative capacity specifically in MerTK+ macrophages. (LLM, conf=0.83)
Experimental — accuracy not yet measuredThis approach can harness EIMP, which stabilizes a reparative phenotype via the DNase2a-DNA-PKcs-mTORC2-Myc axis.
“Mechanistically, this approach can harness pathways such as EIMP, which stabilizes a reparative phenotype via the DNase2a-DNA-PKcs-mTORC2-Myc axis (46).”
From Macrophage duality in liver diseases: heterogeneity, plasticity, and the quest for precision therapeutics (2026) · cites this paper as [46]
The Results (page unavailable) support the Dnase2a–DNA-PKcs–mTORC2–Myc pathway as a driver of efferocytosis-induced macrophage proliferation. The Discussion (page unavailable) says this can expand resolving macrophages and promote plaque stabilization, but does not show that the pathway stabilizes a reparative phenotype within macrophages. (LLM, conf=0.86)
Experimental — accuracy not yet measuredPrevious research suggests a role for lipid metabolism in TAM-mediated efferocytosis.
“This aligns with previous research suggesting a role for lipid metabolism in TAM-mediated efferocytosis.”
From Macrophage efferocytosis mediated by the TP63-RAC2 pathway promotes immunosuppressive remodeling in esophageal cancer (2026) · cites this paper as [16]
The Introduction and Discussion describe lipids from apoptotic cells as contributors to pathways in efferocytosing macrophages. The copy does not establish that lipid metabolism has this role specifically in TAM-mediated efferocytosis; its MerTK results address macrophage proliferation and efferocytosis, not a lipid-metabolism link. (LLM, conf=0.82)
Experimental — accuracy not yet measuredEfferocytosis triggers macrophage proliferation through a defined DNase2a-DNA-PKcs-mTORC2-Myc pathway, termed efferocytosis-induced macrophage proliferation (EIMP).
“Complementing this rapid functional rewiring, efferocytosis itself can trigger macrophage proliferation through a defined DNase2a–DNA-PKcs–mTORC2–Myc pathway — a process termed efferocytosis-induced macrophage proliferation (EIMP).”
From Macrophage duality in liver diseases: heterogeneity, plasticity, and the quest for precision therapeutics (2026) · cites this paper as [46]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
1 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
RetractedMacrophage biology in development, homeostasis and disease
Wynn, T. A., Chawla, A., & Pollard, J. W. (2013) · Nature · doi:10.1038/nature12034 · Cited by 4,684 · see citing works
Fadok, V. A., Bratton, D. L., Konowal, A., Freed, P. W., Westcott, J. Y., & Henson, P. M. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1112 · Cited by 3,166 · see citing works
Identification of a Novel Inhibitor of Mitogen-activated Protein Kinase Kinase
Favata, M. F., Horiuchi, K. Y., Manos, E. J., Daulerio, A. J., Stradley, D. A., Feeser, W. S., Dyk, D. E. V., Pitts, W. J., Earl, R. A., Hobbs, F. W., et al. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.29.18623 · Cited by 3,016 · see citing works
Hashimoto, D., Chow, A., Noizat, C., Teo, P., Beasley, M. B., Leboeuf, M., Becker, C. D., See, P., Price, J., Lucas, D., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.04.004 · Cited by 2,311 · 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
Immunometabolism governs dendritic cell and macrophage function
O'Neill, L. A. J., & Pearce, E. J. (2015) · The Journal of Experimental Medicine · doi:10.1084/jem.20151570 · Cited by 1,715 · see citing works
Jenkins, S., Ruckerl, D., Cook, P., Jones, L., Finkelman, F., van Rooijen, N., MacDonald, A., & Allen, J. (2011) · Science · doi:10.1126/science.1204351 · Cited by 1,427 · 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
Self-citationLocal proliferation dominates lesional macrophage accumulation in atherosclerosis
Robbins, C. S., Hilgendorf, I., Weber, G. F., Theurl, I., Iwamoto, Y., Figueiredo, J.-L., Gorbatov, R., Sukhova, G. K., Gerhardt, L. M. S., Smyth, D., et al. (2013) · Nature Medicine · doi:10.1038/nm.3258 · Cited by 1,041 · 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
Microglia derive from progenitors, originating from the yolk sac, and which proliferate in the brain
Alliot, F., Godin, I., & Pessac, B. (1999) · Developmental Brain Research · doi:10.1016/s0165-3806(99)00113-3 · Cited by 884 · see citing works
Immunobiology of the TAM receptors
Lemke, G., & Rothlin, C. V. (2008) · Nature reviews. Immunology · doi:10.1038/nri2303 · Cited by 867 · 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
TAM receptors regulate multiple features of microglial physiology
Fourgeaud, L., Través, P. G., Tufail, Y., Leal-Bailey, H., Lew, E. D., Burrola, P. G., Callaway, P., Zagórska, A., Rothlin, C. V., Nimmerjahn, A., et al. (2016) · Nature · doi:10.1038/nature17630 · Cited by 600 · see citing works
mTORC2-IRF4 mediated metabolic reprograming is essential for macrophage alternative activation
Huang, S., Smith, A., Everts, B., Colonna, M., Pearce, E. L., Schilling, J., & Pearce, E. J. (2016) · Immunity · doi:10.1016/j.immuni.2016.09.016 · Cited by 579 · see citing works
Macrophage function in tissue repair and remodeling requires IL-4 or IL-13 with apoptotic cells
Bosurgi, L., Cao, Y. G., Cabeza-Cabrerizo, M., Tucci, A., Hughes, L. D., Kong, Y., Weinstein, J. S., Licona-Limon, P., Schmid, E. T., Pelorosso, F., et al. (2017) · Science · doi:10.1126/science.aai8132 · Cited by 560 · see citing works
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
Self-citationZhang, 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
Ras Enhances Myc Protein Stability
Sears, R. C., Leone, G. W., DeGregori, J. V., & Nevins, J. R. (1999) · Molecular Cell · doi:10.1016/s1097-2765(00)80308-1 · Cited by 454 · 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-citationLiving 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
Role of c-MYC in alternative activation of human macrophages and tumor-associated macrophage biology
Pello, Ó. M., Pizzol, M. D., Mirolo, M., Soucek, L., Zammataro, L. A., Amabile, A., Doni, A., Nebuloni, M., Swigart, L. B., Evan, G. I., et al. (2011) · Blood · doi:10.1182/blood-2011-02-339911 · Cited by 387 · see citing works
Interaction of Ku protein and DNA-dependent protein kinase catalytic subunit with nucleic acids
Dynan, W. S., & Yoo, S. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.7.1551 · Cited by 376 · 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
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-citationMcDonald, P. P., Fadok, V. A., Bratton, D. L., & Henson, P. M. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.163.11.6164 · Cited by 350 · see citing works
McDonald, P. P., Fadok, V. A., Bratton, D. L., & Henson, P. M. (1999) · PubMed · Cited by 332 · see citing works
Davies, L. C., Rosas, M., Jenkins, S. J., Liao, C., Scurr, M. J., Brombacher, F., Fraser, D. J., Allen, J. E., Jones, S. A., & Taylor, P. R. (2013) · Nature Communications · doi:10.1038/ncomms2877 · Cited by 332 · see citing works
Camenisch, T. D., Koller, B. H., Earp, H. S., & Matsushima, G. K. (1999) · PubMed · Cited by 321 · see citing works
Rahman, K., Vengrenyuk, Y., Ramsey, S., Vila, N. R., Girgis, N., Liu, J.-H., Gusarova, V., Gromada, J., Weinstock, A., Moore, K., et al. (2017) · Journal of Clinical Investigation · doi:10.1172/jci75005 · Cited by 311 · see citing works
Camenisch, T. D., Koller, B. H., Earp, H. S., & Matsushima, G. K. (1999) · The Journal of Immunology · doi:10.4049/jimmunol.162.6.3498 · Cited by 290 · see citing works
The MYC transcription factor network: balancing metabolism, proliferation and oncogenesis
Carroll, P. A., Freie, B. W., Mathsyaraja, H., & Eisenman, R. N. (2018) · Frontiers of Medicine · doi:10.1007/s11684-018-0650-z · Cited by 289 · see citing works
Okabe, Y., Kawane, K., Akira, S., Taniguchi, T., & Nagata, S. (2005) · The Journal of Experimental Medicine · doi:10.1084/jem.20051654 · Cited by 275 · see citing works
Macrophage MerTK Promotes Liver Fibrosis in Nonalcoholic Steatohepatitis
Cai, B., Dongiovanni, P., Corey, K. E., Wang, X., Shmarakov, I. O., Zheng, Z., Kasikara, C., Davra, V., Meroni, M., Chung, R. T., et al. (2020) · Cell Metabolism · doi:10.1016/j.cmet.2019.11.013 · 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-citationTao, W., Yurdagul, A., Kong, N., Li, W., Wang, X., Doran, A. C., Feng, C., Wang, J., Islam, M. A., Farokhzad, O. C., et al. (2020) · Science Translational Medicine · doi:10.1126/scitranslmed.aay1063 · Cited by 258 · 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-citationContinued 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
Liu, L., Lu, Y., Martinez, J., Bi, Y., Lian, G., Wang, T., Milasta, S., Wang, J., Yang, M., Liu, G., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1518000113 · Cited by 239 · see citing works
Dnase2a deficiency uncovers lysosomal clearance of damaged nuclear DNA via autophagy
Lan, Y. Y., Londoño, D., Bouley, R., Rooney, M. S., & Hacohen, N. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.08.074 · Cited by 236 · see citing works
Davies, L. C., Rosas, M., Smith, P. J., Fraser, D. J., Jones, S. A., & Taylor, P. R. (2011) · European Journal of Immunology · doi:10.1002/eji.201141817 · Cited by 232 · see citing works
Regulatory T Cells License Macrophage Pro-Resolving Functions During Atherosclerosis Regression
Sharma, M., Schlegel, M., Afonso, M., Brown, E. J., Rahman, K., Weinstock, A., Sansbury, B. E., Corr, E. M., van Solingen, C., Koelwyn, G., et al. (2020) · Circulation Research · doi:10.1161/circresaha.119.316461 · Cited by 231 · see citing works
Development and in vivo efficacy of targeted polymeric inflammation-resolving nanoparticles
Kamaly, N., Fredman, G., Subramanian, M., Gadde, S., Pešić, A., Cheung, L., Fayad, Z. A., Langer, R., Tabas, I. A., & Farokhzad, O. C. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1303377110 · Cited by 215 · see citing works
Self-citationHenson, P. M. (2017) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-111315-125315 · Cited by 208 · 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-citationTibrewal, N., Wu, Y., D’Mello, V., Akakura, R., George, T. C., Varnum, B. C., & Birge, R. B. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m706906200 · Cited by 156 · see citing works
MERTK receptor tyrosine kinase is a therapeutic target in melanoma
Schlegel, J., Sambade, M. J., Sather, S., Moschos, S. J., Tan, A. C., Winges, A., DeRyckere, D., Carson, C. C., Trembath, D. G., Tentler, J. J., et al. (2013) · Journal of Clinical Investigation · doi:10.1172/jci67816 · Cited by 149 · see citing works
Self-citationPro-Resolving Mediators in Regulating and Conferring Macrophage Function
Dalli, J., & Serhan, C. N. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.01400 · Cited by 147 · see citing works
Reddy, S. M., Hsiao, K.-C., Abernethy, V. E., Fan, H., Longacre, A., Lieberthal, W., Rauch, J., Koh, J. S., & Levine, J. S. (2002) · The Journal of Immunology · doi:10.4049/jimmunol.169.2.702 · Cited by 110 · see citing works
Bhlhe40 and Bhlhe41 Transcription Factors Regulate Alveolar Macrophage Self‐renewal and Identity
Rauschmeier, R., Gustafsson, C., Reinhardt, A., A‐Gonzalez, N., Tortola, L., Cansever, D., Subramanian, S., Taneja, R., Rossner, M. J., Sieweke, M. H., et al. (2019) · The EMBO Journal · doi:10.15252/embj.2018101233 · Cited by 102 · see citing works
Nishi, C., Yanagihashi, Y., Segawa, K., & Nagata, S. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra118.006628 · Cited by 92 · see citing works
NADPH oxidase activation regulates apoptotic neutrophil clearance by murine macrophages
Bagaitkar, J., Huang, J., Zeng, M. Y., Pech, N. K., Monlish, D. A., Perez‐Zapata, L. J., Miralda, I., Schuettpelz, L. G., & Dinauer, M. C. (2018) · Blood · doi:10.1182/blood-2017-09-809004 · Cited by 82 · see citing works
Jarjour, N. N., Schwarzkopf, E. A., Bradstreet, T. R., Shchukina, I., Lin, C., Huang, S. C., Lai, C., Cook, M. E., Taneja, R., Stappenbeck, T. S., et al. (2019) · Nature Immunology · doi:10.1038/s41590-019-0382-5 · Cited by 82 · see citing works
Sinha, S. K., Miikeda, A., Fouladian, Z., Mehrabian, M., Edillor, C. R., Shih, D. M., Zhou, Z., Paul, M. K., Charugundla, S., Davis, R. C., et al. (2020) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.120.315255 · Cited by 82 · see citing works
Härdtner, C., Kornemann, J., Krebs, K., Ehlert, C. A., Jander, A., Zou, J., Starz, C., Rauterberg, S., Sharipova, D., Dufner, B., et al. (2020) · Basic Research in Cardiology · doi:10.1007/s00395-020-00838-4 · Cited by 66 · see citing works
Differential signaling during macropinocytosis in response to M-CSF and PMA in macrophages
Yoshida, S., Gaeta, I., Pacitto, R., Krienke, L. K., Alge, O., Gregorka, B., & Swanson, J. A. (2015) · Frontiers in Physiology · doi:10.3389/fphys.2015.00008 · Cited by 57 · see citing works
Wnt signaling enhances macrophage responses to IL-4 and promotes resolution of atherosclerosis
Weinstock, A., Rahman, K., Yaacov, O., Nishi, H., Menon, P., Nikain, C. A., Garabedian, M. L., Pena, S., Akbar, N., Sansbury, B. E., et al. (2021) · eLife · doi:10.7554/elife.67932 · Cited by 57 · see citing works
Regression of Atherosclerosis: The Journey From the Liver to the Plaque and Back.
Fisher, E. (2016) · Arteriosclerosis, Thrombosis and Vascular Biology · doi:10.1161/atvbaha.115.301926 · Cited by 55 · see citing works
Xiong, W., Frasch, S. C., Thomas, S. M., Bratton, D. L., & Henson, P. M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0072772 · Cited by 48 · see citing works
Zheng, B., Mao, J., Li, X., Qian, L., Zhu, H., Gu, D., & Pan, X. (2016) · Scientific Reports · doi:10.1038/srep29415 · Cited by 44 · see citing works
Coronary atherosclerosis can regress with very intensive statin therapy.
Sipahi, İ., Nicholls, S. J., Tuzcu, E. M., & Nissen, S. E. (2006) · Cleveland Clinic Journal of Medicine · doi:10.3949/ccjm.73.10.937 · Cited by 42 · see citing works
Willecke, F., Yuan, C., Oka, K., Chan, L., Hu, Y., Barnhart, S., Bornfeldt, K., Goldberg, I. J., & Fisher, E. A. A. (2015) · PLoS ONE · doi:10.1371/journal.pone.0128996 · Cited by 40 · see citing works
Pashover‐Schallinger, E., Aswad, M., Schif‐Zuck, S., Shapiro, H., Singer, P., & Ariel, A. (2012) · The FASEB Journal · doi:10.1096/fj.11-194894 · Cited by 34 · see citing works
Babaev, V. R., Huang, J., Ding, L., Zhang, Y., May, J. M., & Linton, M. F. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00215 · Cited by 26 · see citing works
Self-renewing macrophages – A new line of enquiries in mononuclear phagocytes
Fejér, G., Sharma, S., & Győry, I. (2014) · Immunobiology · doi:10.1016/j.imbio.2014.11.005 · Cited by 24 · see citing works
Macrophage NCOR1 Deficiency Ameliorates Myocardial Infarction and Neointimal Hyperplasia in Mice
Du, L., Sun, J., Zhang, W., Wang, Y., Zhu, H., Liu, T., Gao, M., Zheng, C., Zhang, Y., Liu, Y., et al. (2020) · Journal of the American Heart Association · doi:10.1161/jaha.120.015862 · Cited by 23 · see citing works
Minchew, C. L., & Didenko, V. V. (2011) · Molecules · doi:10.3390/molecules16064599 · Cited by 19 · see citing works
Morita, Y., Senokuchi, T., Yamada, S., Wada, T., Furusho, T., Matsumura, T., Ishii, N., Nishida, S., Nishida, S., Motoshima, H., et al. (2020) · BMJ Open Diabetes Research & Care · doi:10.1136/bmjdrc-2020-001578 · Cited by 12 · see citing works
Subramanian, M., Proto, J. D., Matsushima, G. K., & Tabas, I. A. (2016) · Scientific Reports · doi:10.1038/srep39111 · Cited by 10 · see citing works
Self-citation
Flagged first, then by citations
Cited by
Sorted by citations
Atherosclerosis: Recent developments
Björkegren, J., & Lusis, A. J. (2022) · Cell · doi:10.1016/j.cell.2022.04.004 · Cited by 1,301 · see citing works
Inflammation and atherosclerosis: signaling pathways and therapeutic intervention
Kong, P., Cui, Z.-Y., Huang, X.-F., Zhang, D.-D., Guo, R.-J., & Han, M. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-00955-7 · Cited by 1,183 · 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
Tissue macrophages: origin, heterogenity, biological functions, diseases and therapeutic targets
Guan, F., Wang, R., Yi, Z., Luo, P., Liu, W., Xie, Y., Liu, Z., Xia, Z., Zhang, H., & Cheng, Q. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02124-y · Cited by 371 · see citing works
Macrophage polarization and metabolism in atherosclerosis
Hou, P., Fang, J., Liu, Z., Shi, Y., Agostini, M., Bernassola, F., Bove, P., Candi, E., Rovella, V., Sica, G. S., et al. (2023) · Cell Death and Disease · doi:10.1038/s41419-023-06206-z · Cited by 360 · see citing works
Macrophage phenotypes and functions: resolving inflammation and restoring homeostasis
Rodríguez-Morales, P., & Franklin, R. A. (2023) · Trends in Immunology · doi:10.1016/j.it.2023.10.004 · Cited by 327 · see citing works
Hilgendorf, I., Frantz, S., & Frangogiannis, N. G. (2024) · Circulation Research · doi:10.1161/circresaha.124.323658 · Cited by 200 · see citing works
The role of efferocytosis‐fueled macrophage metabolism in the resolution of inflammation
Schilperoort, M., Ngai, D., Sukka, S. R., Avrampou, K., Shi, H., & Tabas, I. A. (2023) · Immunological Reviews · doi:10.1111/imr.13214 · Cited by 181 · see citing works
Self-citationAmpomah, P. B., Cai, B., Sukka, S. R., Gerlach, B. D., Yurdagul, A., Wang, X., Kuriakose, G., Darville, L. N. F., Sun, Y., Sidoli, S., et al. (2022) · Nature Metabolism · doi:10.1038/s42255-022-00551-7 · Cited by 176 · see citing works
Self-citationInflammation Resolution: Implications for Atherosclerosis
Doran, A. C. (2022) · Circulation Research · doi:10.1161/circresaha.121.319822 · Cited by 177 · 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
PFKFB2-mediated glycolysis promotes lactate-driven continual efferocytosis by macrophages
Schilperoort, M., Ngai, D., Katerelos, M., Power, D., & Tabas, I. (2023) · Nature Metabolism · doi:10.1038/s42255-023-00736-8 · Cited by 145 · see citing works
Self-citationEfferocytosis and Its Role in Inflammatory Disorders
Ge, Y., Huang, M., & Yao, Y.-M. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.839248 · Cited by 139 · 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
Crosstalk Between Macrophages and Vascular Smooth Muscle Cells in Atherosclerotic Plaque Stability
Yurdagul, A. (2022) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.121.316233 · Cited by 137 · see citing works
Self-citationGong, S., Zhai, M., Shi, J.-Y., Yu, G., Lei, Z.-J., Shi, Y.-F., Zeng, Y.-X., Ju, P.-Q., Yang, N., Zhang, Z., et al. (2024) · Cell Death and Differentiation · doi:10.1038/s41418-023-01252-8 · Cited by 120 · see citing works
Self-citationHigh-Dimensional Single-Cell Multimodal Landscape of Human Carotid Atherosclerosis
Bashore, A. C., Yan, H., Xue, C., Zhu, L. Y., Kim, E., Mawson, T. L., Coronel, J., Chung, A. Y., Sachs, N., Ho, S., et al. (2024) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.123.320524 · Cited by 121 · see citing works
The immune system in cardiovascular diseases: from basic mechanisms to therapeutic implications
Wang, X., Chen, L., Wei, J., Zheng, H., Zhou, N., Xu, X., Deng, X., Liu, T., & Zou, Y. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02220-z · Cited by 120 · see citing works
Self-citationSenescent cells suppress macrophage-mediated corpse removal via upregulation of the CD47-QPCT/L axis
Schloesser, D., Lindenthal, L., Sauer, J., Chung, K., Chavakis, T., Griesser, E., Baskaran, P., Maier-Habelsberger, U., Fundel‐Clemens, K., Schlotthauer, I., et al. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202207097 · Cited by 113 · see citing works
Nanomedicine for Diagnosis and Treatment of Atherosclerosis
Cheng, J., Huang, H., Chen, Y., & WU, R. T. (2023) · Advanced Science · doi:10.1002/advs.202304294 · Cited by 115 · see citing works
Macrophages Orchestrate Airway Inflammation, Remodeling, and Resolution in Asthma
Britt, R. D., Ruwanpathirana, A., Ford, M. L., & Lewis, B. W. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310451 · Cited by 115 · see citing works
He, H., Han, Q., Wang, S., Long, M., Zhang, M., Li, Y., Zhang, Y., & Gu, N. (2023) · ACS Nano · doi:10.1021/acsnano.3c01420 · Cited by 107 · see citing works
Through the layers: how macrophages drive atherosclerosis across the vessel wall
Susser, L. I., & Rayner, K. J. (2022) · Journal of Clinical Investigation · doi:10.1172/jci157011 · Cited by 99 · see citing works
Ngai, D., Schilperoort, M., & Tabas, I. A. (2023) · Nature Metabolism · doi:10.1038/s42255-023-00921-9 · Cited by 99 · see citing works
Self-citationDiabetic Wound Repair: From Mechanism to Therapeutic Opportunities
Wang, R., Gu, S., Kim, Y. H., Lee, A., Lin, H., & Jiang, D. (2025) · MedComm · doi:10.1002/mco2.70406 · Cited by 111 · see citing works
Apoptotic cell identity induces distinct functional responses to IL-4 in efferocytic macrophages
Liebold, I., Al Jawazneh, A., Casar, C., Lanzloth, C., Leyk, S., Hamley, M., Wong, M. N., Kylies, D., Gräfe, S. K., Edenhofer, I., et al. (2024) · Science · doi:10.1126/science.abo7027 · Cited by 96 · see citing works
Zhu, Y.-H., Zheng, J.-H., Jia, Q.-Y., Duan, Z., Yao, H., Yang, J., Sun, Y., Jiang, S.-H., Liu, D., & Huo, Y. (2022) · Cellular Oncology · doi:10.1007/s13402-022-00741-1 · Cited by 96 · see citing works
Ji, Y.-N., Li, X., Yao, X.-L., Sun, J., Yi, J., Shen, Y.-T., Chen, B.-Q., & Sun, H.-L. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1732718 · Cited by 93 · see citing works
Giacomini, C., Granéli, C., Hicks, R., & Dazzi, F. (2023) · Cellular and Molecular Immunology · doi:10.1038/s41423-023-01018-9 · Cited by 91 · see citing works
Chou, M., Babamale, A. O., Walker, T. L., Cognasse, F., Blum, D. L., & Burnouf, T. P. R. (2023) · Trends in Neurosciences · doi:10.1016/j.tins.2023.06.005 · Cited by 84 · see citing works
You, Y., Xu, J., Liu, Y., Li, H., Xie, L., Ma, C., Sun, Y., Tong, S., Liang, K., Zhou, S., et al. (2023) · ACS Nano · doi:10.1021/acsnano.3c01497 · Cited by 83 · see citing works
Efferocytosis drives a tryptophan metabolism pathway in macrophages to promote tissue resolution
Sukka, S. R., Ampomah, P. B., Darville, L. N. F., Ngai, D., Wang, X., Kuriakose, G., Xiao, Y., Shi, J., Koomen, J. M., McCusker, R. H., et al. (2024) · Nature Metabolism · doi:10.1038/s42255-024-01115-7 · Cited by 82 · see citing works
Self-citationWang, H., Zhang, Y., Zhang, Y., Li, C., Zhang, M., Wang, J., Zhang, Y., Du, Y., Cui, W., & Chen, W. (2024) · Advanced Materials · doi:10.1002/adma.202402968 · Cited by 76 · 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
Self-citationWang, W., Chu, Y., Zhang, P., Liang, Z., Fan, Z., Guo, X., Zhou, G., & Ren, W. (2023) · International Immunopharmacology · doi:10.1016/j.intimp.2023.109790 · Cited by 70 · see citing works
Epsin Nanotherapy Regulates Cholesterol Transport to Fortify Atheroma Regression
Cui, K., Gao, X., Wang, B., Wu, H., Kulandaisamy, A., Dong, Y., Xiao, Y., Jiang, X., Malovichko, M. V., Li, K. S., et al. (2022) · Circulation Research · doi:10.1161/circresaha.122.321723 · Cited by 65 · see citing works
Self-citationMacrophages: a double-edged sword in female reproduction and disorders
Park, M., Kim, Y. S., & Song, H. (2025) · Experimental & Molecular Medicine · doi:10.1038/s12276-025-01392-6 · Cited by 63 · see citing works
Cardiac macrophages and emerging roles for their metabolism after myocardial infarction
Thorp, E. B. (2023) · Journal of Clinical Investigation · doi:10.1172/jci171953 · Cited by 64 · see citing works
Hamidzada, H., Pascual‐Gil, S., Wu, Q., Kent, G. M., Massé, S., Kantores, C., Kuzmanov, U., Gomez-Garcia, M. J., Rafatian, N., Gorman, R. A., et al. (2024) · Nature Cardiovascular Research · doi:10.1038/s44161-024-00471-7 · Cited by 62 · see citing works
Macrophage variants in laboratory research: most are well done, but some are RAW
Herb, M., Schatz, V., Hadrian, K., Hos, D., Holoborodko, B., Jantsch, J., & Brigo, N. (2024) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2024.1457323 · Cited by 63 · see citing works
SIRT3 Regulates Clearance of Apoptotic Cardiomyocytes by Deacetylating Frataxin
Gao, J., Huang, C., Kong, L., Zhou, W., Sun, M., Wei, T., & Shen, W. (2023) · Circulation Research · doi:10.1161/circresaha.123.323160 · Cited by 60 · see citing works
Challenges for Clinical Drug Development in Pulmonary Fibrosis
White, E. S., Thomas, M. J., Stowasser, S., & Tetzlaff, K. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.823085 · Cited by 58 · see citing works
Chen, Z., Li, Z., Huang, H., Shen, G., Ren, Y., Mao, X., Wang, L., Li, Z., Wang, W., Li, G., et al. (2023) · Small · doi:10.1002/smll.202302758 · Cited by 58 · see citing works
Xiong, W., Han, Z., Ding, S., Wang, H., Du, Y., Cui, W., & Zhang, M. (2024) · Advanced Science · doi:10.1002/advs.202400345 · Cited by 57 · see citing works
Tanshinone IIA: a Chinese herbal ingredient for the treatment of atherosclerosis
Yang, C., Yan-guang, M., Li, S., Zhang, Y., Liu, X., & Li, J. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1321880 · Cited by 52 · see citing works
Resolution therapy: Harnessing efferocytic macrophages to trigger the resolution of inflammation
Saas, P., Vetter, M., Maraux, M., Bonnefoy, F., & Perruche, S. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1021413 · Cited by 52 · see citing works
Global Characteristics and Dynamics of Single Immune Cells After Myocardial Infarction
Zhuang, L., Wang, Y., Chen, Z., Li, Z., Wang, Z., Jia, K., Zhao, J., Zhang, H., Xie, H., Lu, L., et al. (2022) · Journal of the American Heart Association · doi:10.1161/jaha.122.027228 · Cited by 51 · see citing works
Qiu, S., Liu, J., Chen, J., Li, Y., Bu, T., Li, Z., Zhang, L., Sun, W., Zhou, T., Hu, W., et al. (2024) · Journal of Nanobiotechnology · doi:10.1186/s12951-024-02463-y · Cited by 50 · see citing works
Induction of osteoblast apoptosis stimulates macrophage efferocytosis and paradoxical bone formation
Batoon, L., Koh, A. J., Millard, S. M., Grewal, J., Choo, F. M., Kannan, R., Kinnaird, A., Avey, M., Teslya, T., Pettit, A. R., et al. (2024) · Bone Research · doi:10.1038/s41413-024-00341-9 · Cited by 51 · see citing works
Lysosomes in the immunometabolic reprogramming of immune cells in atherosclerosis
Bonacina, F., Zhang, X., Manel, N., Yvan‐Charvet, L., Razani, B., & Norata, G. D. (2024) · Nature Reviews Cardiology · doi:10.1038/s41569-024-01072-4 · Cited by 50 · see citing works
Multifaceted mitochondrial quality control in brown adipose tissue
Aquilano, K., Zhou, B., Brestoff, J. R., & Lettieri‐Barbato, D. (2022) · Trends in Cell Biology · doi:10.1016/j.tcb.2022.09.008 · Cited by 47 · see citing works
Bhattacharya, P., Dhawan, U. K., Hussain, M. T., Singh, P., Bhagat, K. K., Singhal, A., Austin‐Williams, S., Sengupta, S., & Subramanian, M. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112808 · Cited by 48 · see citing works
Macrophage heterogeneity and efferocytosis: Beyond the M1/M2 dichotomy
Kumar Jha, P., Aikawa, M., & Aikawa, E. (2024) · Circulation Research · doi:10.1161/circresaha.123.324011 · Cited by 45 · see citing works
Loss of Macrophage mTORC2 Drives Atherosclerosis via FoxO1 and IL-1β Signaling
Zhang, X., Evans, T. D., Chen, S., Sergin, I., Stitham, J., Jeong, S., Rodríguez-Vélez, A., Yeh, Y., Park, A. C., Jung, I., et al. (2023) · Circulation Research · doi:10.1161/circresaha.122.321542 · Cited by 44 · see citing works
Self-citationJeelani, I., Moon, J.-S., da Cunha, F. F., Nasamran, C., Jeon, S., Zhang, X.-H., Bandyopadhyay, G. K., Dobaczewska, K., Mikulski, Z., Hosseini, M., et al. (2024) · Science Translational Medicine · doi:10.1126/scitranslmed.adi0284 · Cited by 46 · see citing works
Emerging roles of neutrophils in immune homeostasis
Lee, M., Lee, S. Y., & Bae, Y. (2022) · BMB Reports · doi:10.5483/bmbrep.2022.55.10.115 · Cited by 41 · see citing works
Rapid unleashing of macrophage efferocytic capacity via transcriptional pause release
Tufan, T., Cömertpay, G., Villani, A., Nelson, G. M., Terekhova, M., Kelley, S. M., Zakharov, P. N., Ellison, R. M., Shpynov, O., Raymond, M. H., et al. (2024) · Nature · doi:10.1038/s41586-024-07172-y · Cited by 41 · see citing works
The interplay between nonalcoholic fatty liver disease and atherosclerotic cardiovascular disease
Finney, A. C., Das, S., Kumar, D., McKinney, M. P., Cai, B., Yurdagul, A., & Rom, O. (2023) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2023.1116861 · Cited by 40 · see citing works
Self-citationFerroptotic MSCs protect mice against sepsis via promoting macrophage efferocytosis
Pan, Y., Li, J., Wang, J., Jiang, Q., Yang, J., Dou, H., Liang, H., Li, K., & Hou, Y. (2022) · Cell Death and Disease · doi:10.1038/s41419-022-05264-z · Cited by 40 · see citing works
Liu, W., Hardaway, B. D., Kim, E., Pauli, J., Wettich, J. L., Yalçınkaya, M., Hsu, C.-C., Xiao, T., Reilly, M. P., Tabas, I. A., et al. (2024) · Journal of Clinical Investigation · doi:10.1172/jci182939 · Cited by 36 · see citing works
Self-citationRetinoic acid signaling in development and differentiation commitment and its regulatory topology
Wu, D., Khan, F. A., Zhang, K., Pandupuspitasari, N. S., Negara, W., Guan, K., Sun, F., & Huang, C. (2023) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2023.110773 · Cited by 37 · see citing works
Targeting persistently activated inflammatory microenvironment to promote chronic wound healing
Dai, Y., & Chen, Y. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1708358 · Cited by 38 · see citing works
Zhang, J., Ding, W. B., Zhao, M., Liu, J., Xu, Y., Wan, J., & Wang, M. (2022) · British Journal of Pharmacology · doi:10.1111/bph.15939 · Cited by 37 · see citing works
Yin, Z., Zhang, J., Zhao, M., Liu, J., Xu, Y. Q., Peng, S., Pan, W. D., Wei, C., Zheng, Z., Liu, S., et al. (2024) · Autophagy · doi:10.1080/15548627.2024.2367191 · Cited by 35 · see citing works
Impaired Efferocytosis Enables Apoptotic Osteoblasts to Escape Osteoimmune Surveillance During Aging
Xu, R., Xie, H., Shen, X., Huang, J., Zhang, H., Fu, Y., Zhang, P., Guo, S., Wang, D., Li, S., et al. (2023) · Advanced Science · doi:10.1002/advs.202303946 · Cited by 34 · see citing works
Zaid, A. K. M. A., & Ariel, A. (2024) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2024.115204 · Cited by 35 · see citing works
The Atherosclerotic Plaque Microenvironment as a Therapeutic Target
Pandit, R., & Yurdagul, A. (2025) · Current Atherosclerosis Reports · doi:10.1007/s11883-025-01294-y · Cited by 33 · see citing works
Self-citationMechanisms of continual efferocytosis by macrophages and its role in mitigating atherosclerosis
Kumar, D., Pandit, R., & Yurdagul, A. (2023) · Immunometabolism · doi:10.1097/in9.0000000000000017 · Cited by 35 · see citing works
Self-citationRole of Resolvins in Inflammatory and Neuropathic Pain
Park, J., Roh, J., Pan, J., Kim, Y. H., Park, C., & Jo, Y. Y. (2023) · Pharmaceuticals · doi:10.3390/ph16101366 · Cited by 32 · see citing works
Xia, W., Zhu, Z., Xiang, S., & Yang, Y. (2023) · Journal of Ginseng Research · doi:10.1016/j.jgr.2023.06.006 · Cited by 31 · see citing works
Efferocytosis: Unveiling its potential in autoimmune disease and treatment strategies
Xing, J., Wang, K., Xu, Y.-C., Pei, Z.-J., Yu, Q., Liu, X., Dong, Y.-L., Li, S., Chen, Y., Zhao, Y., et al. (2024) · Autoimmunity Reviews · doi:10.1016/j.autrev.2024.103578 · Cited by 31 · see citing works
Cheng, M., Yu, X., Qi, S., Yang, K., Lu, M., Cao, F., & Yu, G. (2024) · Angewandte Chemie International Edition · doi:10.1002/anie.202407398 · Cited by 31 · see citing works
Hoseinzadeh, A., Esmaeili, S., Sahebi, R., Melak, A. M., Mahmoudi, M., Hasannia, M., & Baharlou, R. (2025) · Stem Cell Research & Therapy · doi:10.1186/s13287-025-04158-z · Cited by 34 · see citing works
Macrophages in tissue repair and regeneration: insights from zebrafish
Zhao, C., Yang, Z., Li, Y., & Wen, Z. (2024) · Cell Regeneration · doi:10.1186/s13619-024-00195-w · Cited by 30 · see citing works
Role of inflammation and evidence for the use of colchicine in patients with acute coronary syndrome
Bulnes, J. F., González, L., Velásquez, L., Paz, O. M., Venturelli, P. M., & Martínez, G. (2024) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2024.1356023 · Cited by 29 · see citing works
Tsai, T., Zhou, T.-A., Hsieh, Y., Wang, J.-C., Cheng, H.-K., Huang, C., Tsai, P.-Y., Fan, H.-H., Feng, H.-K., Huang, Y. Y., et al. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111065 · Cited by 29 · see citing works
Liu, Y., Xue, R., Duan, X., Shang, X., Wang, M., Wang, F., Zhu, L., Zhang, L., Ge, X., Zhao, X., et al. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.121790 · Cited by 28 · see citing works
Innovative Atherosclerosis Models: Advancing Pathophysiology and Translational Research
Jiang, H., Liao, Y., Zhu, M., Jiramonai, L., Wu, H., Zhong, Y., Xie, Z., & Liang, X. (2025) · Research · doi:10.34133/research.0617 · Cited by 28 · see citing works
Qiang, P., Hao, J., Yang, F., Han, Y., Chang, Y. Y., Xian, Y., Xiong, Y., Gao, X., Liang, L.-J., Shimosawa, T., et al. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.948658 · Cited by 28 · 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
Cell type–specific efferocytosis determines functional plasticity of alveolar macrophages
Better, J., Estiri, M., Wetstein, M., Pervizaj-Oruqaj, L., Malainou, C., Ogungbemi-Alt, V. K., Ferrero, M. R., Langelage, M., Kuznetsova, I., Vazquez‐Armendariz, A. I., et al. (2025) · Science Immunology · doi:10.1126/sciimmunol.adl3852 · Cited by 27 · see citing works
Nature-inspired nanocarriers for improving drug therapy of atherosclerosis
Ji, W., Zhang, Y., Deng, Y., Li, C., Kankala, R. K., & Chen, A. (2023) · Regenerative Biomaterials · doi:10.1093/rb/rbad069 · Cited by 28 · see citing works
Immunosenescence and macrophages: From basics to therapeutics
Zhu, H., Shen, F., Liao, T., Qian, H., & Liu, Y. (2023) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2023.106479 · Cited by 28 · see citing works
Periodontal Ligament Cell Apoptosis Activates Lepr+ Osteoprogenitors in Orthodontics
Liu, H., Zhang, Y., Zhang, Y., Huang, Y., Yang, Y., Zhao, Y., Chen, S., Deng, J., Li, W., & Han, B. (2024) · Journal of Dental Research · doi:10.1177/00220345241262706 · Cited by 26 · see citing works
Vascular homeostasis in atherosclerosis: A holistic overview
Xu, S., Lyu, Q., Ilyas, I., Tian, X.-Y., & Weng, J. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.976722 · Cited by 26 · see citing works
Chen, J., Wang, Z., Liu, S., Zhao, R., Chen, Q., Li, X., Zhang, S., & Wang, J. (2024) · ACS Nano · doi:10.1021/acsnano.4c11622 · Cited by 25 · see citing works
Kim, S., Kim, Y. K., Kim, S., Choi, Y., Lee, I., Joo, H., Kim, J., Kwon, M., Park, S., Jo, M. K., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-57133-w · Cited by 25 · see citing works
The formation and consequences of cholesterol-rich deposits in atherosclerotic lesions
Maxfield, F. R., Steinfeld, N., & Ma, C.-I. J. (2023) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2023.1148304 · Cited by 25 · see citing works
Biomimetic “Trojan Horse” Fibers Modulate Innate Immunity Cascades for Nerve Regeneration
Wu, J., Tang, J., Zhang, L., Wang, W., Li, Z., Zhou, L., Jiang, X., Huang, Y., Guo, Q., Wang, W., et al. (2024) · ACS Nano · doi:10.1021/acsnano.4c12036 · Cited by 24 · see citing works
IRF5 siRNA Nanoimmunotherapy: Restoring Macrophage Efferocytosis in Atherosclerosis
He, Z., Luo, Y., Duan, Z., Su, B., Zeng, W., Guo, Y., Li, Y., He, X., Shi, H., Zhou, Z., et al. (2025) · Circulation · doi:10.1161/circulationaha.125.075352 · Cited by 24 · see citing works
Macrophages in Atheromatous Plaque Developmental Stages
von Ehr, A., Bode, C., & Hilgendorf, I. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.865367 · Cited by 23 · see citing works
Li, Y., Lv, J., Liu, S., Wang, Z., Gao, Y., Fan, Z., Huang, L., Cui, J., Zhang, B., Liu, X., et al. (2024) · Biomaterials · doi:10.1016/j.biomaterials.2024.122867 · Cited by 23 · see citing works
Hou, F., Wang, H., Zheng, K., Yang, W., Xiao, K., Rong, Z., Xiao, J., Li, J., Cheng, B., Tang, L., et al. (2023) · Immune Network · doi:10.4110/in.2023.23.e24 · Cited by 23 · see citing works
Tanshinone IIA alleviates atherosclerosis in LDLR−/− mice by regulating efferocytosis of macrophages
Wang, J., Zhang, Y., Feng, X., Du, M., Li, S., Chang, X., & Liu, P. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1233709 · Cited by 23 · see citing works
A macrophage-collagen fragment axis mediates subcutaneous adipose tissue remodeling in mice
Vujičić, M., Broderick, I., Salmantabar, P., Perian, C., Nilsson, J., Sihlbom, C., & Asterholm, I. W. (2024) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2313185121 · Cited by 21 · 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
Zeng, L., Wang, Y., Huang, Y., Yang, W., Zhou, P., Wan, Y., Tao, K., & Li, R. (2025) · Cell Communication and Signaling · doi:10.1186/s12964-025-02075-5 · Cited by 22 · see citing works
Peng, L., Song, H., Shi, H., Wu, L., Ma, Y., Fan, X., Wu, M., Duan, L., Li, Z., & Yuan, H. (2025) · ACS Nano · doi:10.1021/acsnano.5c10625 · Cited by 22 · see citing works
Wang, Y., Pu, C., Han, Z., Du, Y., Chen, L., Huang, Y., Luo, Y., Xiang, C., He, J., Chen, L., et al. (2025) · Small · doi:10.1002/smll.202405236 · Cited by 21 · see citing works
Wang, H., Gao, Y., Wang, J., Cao, M., Dai, G.-C., Lu, P., Sheng, R., Zhang, C., Wang, Q., Li, G., et al. (2025) · ACS Nano · doi:10.1021/acsnano.4c16917 · Cited by 21 · see citing works
- Authors
- Gerlach, B. D., Ampomah, P. B., Yurdagul, A., Liu, C., Lauring, M. C., Wang, X., Kasikara, C., Kong, N., Shi, J., Tao, W., & Tabas, I.
- Affiliations
- Columbia University Irving Medical Center (US)
- Brigham and Women's Hospital (US)
- Corresponding author
- Tabas, Ira
- ORCID
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2021-12
- Volume
- 33
- Issue
- 12
- Pages
- 2445-2463.e8
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC8665147
- OpenAlex
- W3212263362
- Cited by
- 360
- References
- 71
- Citations by year
- 2026: 79 · 2025: 105 · 2024: 91 · 2023: 53 · 2022: 31 · 2021: 1
- FWCI
- 16.70
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 371 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (R35 HL145228, K99 HL145131, P20 GM121307, P30CA013696, R01 HL087123, R01 HL127464, S10OD020056, S10RR025686, S10RR027050, T32 5T32HL007343-42)
- American Heart Association (20POST35210962)
- Harvard Medical School (122829)
- 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
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Keywords
- efferocytosis, macrophage proliferation, DNA-PKcs, mTORC2, Rictor, c-Myc, atherosclerosis regression, plaque stabilization, peritonitis, thymocyte apoptosis, phagolysosomes
- MeSH terms
- Animals, Macrophages, Mice, Inbred C57BL, Phagocytosis, Apoptosis, Cell Proliferation, 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