The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index.
Dysregulation of monocyte/macrophage phenotype in wounds of diabetic mice
Abstract
The hypothesis of this study was that cells of the monocyte/macrophage lineage (Mo/Mp) exhibit an impaired transition from pro-inflammatory to pro-healing phenotypes in wounds of diabetic mice, which contributes to deficient healing. Mo/Mp isolated from excisional wounds in non-diabetic db/+ mice exhibited a pro-inflammatory phenotype on day 5 post-injury, with high level expression of the pro-inflammatory molecules interleukin-1β, matrix metalloprotease-9 and inducible nitric oxide synthase. Wound Mo/Mp exhibited a less inflammatory phenotype on day 10 post-injury, with decreased expression of the pro-inflammatory molecules and increased expression of the alternative activation markers CD206 and CD36. In contrast, in db/db mice, the pro-inflammatory phenotype persisted through day 10 post-injury and was associated with reduced expression of insulin-like growth factor-1, transforming growth factor-β1 and vascular endothelial growth factor. Reduced levels of these growth factors in wounds of db/db mice may have contributed to impaired wound closure, reduced granulation tissue formation, angiogenesis and collagen deposition. The persistent pro-inflammatory wound Mo/Mp phenotype in db/db mice may have resulted from elevated levels of pro-inflammatory interleukin-1β and interferon-γ and reduced levels of anti-inflammatory interleukin-10 in the wound environment. Our findings are consistent with the hypothesis that dysregulation of Mo/Mp phenotypes contributes to impaired healing of diabetic wounds.
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In the citing paper
“We recently demonstrated that Mp exhibit a sustained proinflammatory phenotype in wounds of diabetic mice (14)”
From Sustained Inflammasome Activity in Macrophages Impairs Wound Healing in Type 2 Diabetic Humans and Mice (2014) · cites this paper as [14]
In the citing paper
“Bone marrow transfer from wild-type to db/db mice resulted in wound healing that was similar to db/db mice that had not received bone marrow transfer (compare Fig. 7A–D with Fig. 6A–D and refs. 14,15)”
From Sustained Inflammasome Activity in Macrophages Impairs Wound Healing in Type 2 Diabetic Humans and Mice (2014) · cites this paper as [14]
In the citing paper
“We and others have observed a persistent proinflammatory wound Mp phenotype in diabetic humans and mice (14,29) and in chronic venous ulcers (30).”
From Sustained Inflammasome Activity in Macrophages Impairs Wound Healing in Type 2 Diabetic Humans and Mice (2014) · cites this paper as [14]
In the citing paper
“Recent studies have shown that Mp phenotypes change over the different phases of tissue repair and that the sequential appearance of these phenotypes may be required for efficient repair (11,14,29,49,50).”
From Sustained Inflammasome Activity in Macrophages Impairs Wound Healing in Type 2 Diabetic Humans and Mice (2014) · cites this paper as [14]
In the citing paper
“In fact, either premature changes in phenotype or delayed/impaired changes in phenotype have been associated with impaired healing (14,29,49).”
From Sustained Inflammasome Activity in Macrophages Impairs Wound Healing in Type 2 Diabetic Humans and Mice (2014) · cites this paper as [14]
In the citing paper
“Indeed, in mouse and human skin wounds and in injured mouse kidney, Mp expression of CD206 increases during the later stages of repair [33,60,61,63].”
From Macrophage phenotypes during tissue repair (2013) · cites this paper as [60]
In the citing paper
“In mouse skin wounds, IL-4 mRNA and protein are not detectable at early or late time-points [60,71].”
From Macrophage phenotypes during tissue repair (2013) · cites this paper as [60]
In the citing paper
“Mp expression of mRNA and protein for these cytokines exhibits an early peak and subsequent decline after skin wounding [33,60] or toxin-induced muscle injury in mice [65], consistent with an early M1-like phenotype.”
From Macrophage phenotypes during tissue repair (2013) · cites this paper as [60]
In the citing paper
“The M1-associated cytokines IL-1, TNF-␣, IL-6, and IL-12 are expressed by Mp during the first few hours to days after acute injury in numerous tissues, including skin [33,60,61], liver [62], kidney [63], and skeletal muscle [57,64].”
From Macrophage phenotypes during tissue repair (2013) · cites this paper as [60]
In the citing paper
“Indeed, during mouse skin wound healing, Mp expression of TGF- mRNA and protein increases over the first 7-10 days postinjury, whereas proinflammatory cytokine production decreases [33,60], consistent with the expression of an M2a-like phenotype during the later stages of repair.”
From Macrophage phenotypes during tissue repair (2013) · cites this paper as [60]
In the citing paper
“Additionally, a comprehensive in vivo Mp phenotype cannot be deduced solely from a limited set of phenotypic markers, as different M2a-associated genes or proteins can exhibit entirely different temporal regulation and can be coexpressed with M1-associated markers [19,25,33,60,78].”
From Macrophage phenotypes during tissue repair (2013) · cites this paper as [60]
Citations
Cites
Exploring the full spectrum of macrophage activation
Mosser, D. M., & Edwards, J. P. (2008) · Nature Reviews Immunology · doi:10.1038/nri2448 · Cited by 9,144
The chemokine system in diverse forms of macrophage activation and polarization
MANTOVANI, A., SICA, A., SOZZANI, S., ALLAVENA, P., VECCHI, A., & LOCATI, M. (2004) · Trends in Immunology · doi:10.1016/j.it.2004.09.015 · Cited by 6,534
Alternative activation of macrophages
Gordon, S. (2003) · Nature Reviews Immunology · doi:10.1038/nri978 · Cited by 6,189
Blood Monocytes Consist of Two Principal Subsets with Distinct Migratory Properties
Geissmann, F., Jung, S., & Littman, D. R. (2003) · Immunity · doi:10.1016/s1074-7613(03)00174-2 · Cited by 3,504
Human skin wounds: A major and snowballing threat to public health and the economy
Sen, C. K., Gordillo, G. M., Roy, S., Kirsner, R., Lambert, L., Hunt, T. K., Gottrup, F., Gurtner, G. C., & Longaker, M. T. (2009) · Wound Repair and Regeneration · doi:10.1111/j.1524-475x.2009.00543.x · Cited by 2,965
Alternative Activation of Macrophages: An Immunologic Functional Perspective
Martinez, F. O., Helming, L., & Gordon, S. (2009) · Annual Review of Immunology · doi:10.1146/annurev.immunol.021908.132532 · Cited by 2,745
Nahrendorf, M., Swirski, F. K., Aikawa, E., Stangenberg, L., Wurdinger, T., Figueiredo, J.-L., Libby, P., Weissleder, R., & Pittet, M. J. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070885 · Cited by 2,300
Arnold, L., Henry, A., Poron, F., Baba-Amer, Y., van Rooijen, N., Plonquet, A., Gherardi, R. K., & Chazaud, B. (2007) · The Journal of Experimental Medicine · doi:10.1084/jem.20070075 · Cited by 2,002
The role of the macrophage in wound repair. A study with hydrocortisone and antimacrophage serum.
(1975) · PubMed Central · Cited by 1,437
Differential Roles of Macrophages in Diverse Phases of Skin Repair
Lucas, T., Waisman, A., Ranjan, R., Roes, J., Krieg, T., Müller, W., Roers, A., & Eming, S. A. (2010) · The Journal of Immunology · doi:10.4049/jimmunol.0903356 · Cited by 1,205
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Shapouri‐Moghaddam, A., Mohammadian, S., Vazini, H., Taghadosi, M., Esmaeili, S., Mardani, F., Seifi, B., Mohammadi, A., Afshari, J. T., & Sahebkar, A. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.26429 · Cited by 4,930
Krzyszczyk, P., Schloss, R. S., Palmer, A. F., & Francois Berthiaume, B. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.00419 · Cited by 1,598
Vascular Endothelial Growth Factor and Angiogenesis in the Regulation of Cutaneous Wound Repair
Johnson, K. E., & Wilgus, T. A. (2014) · Advances in Wound Care · doi:10.1089/wound.2013.0517 · Cited by 1,169
Diabetes and Wound Angiogenesis
Okonkwo, U. A., & DiPietro, L. A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071419 · Cited by 1,071
Macrophage Phenotypes Regulate Scar Formation and Chronic Wound Healing
Hesketh, M., Sahin, K. B., West, Z. E., & Murray, R. Z. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18071545 · Cited by 852
Macrophage activation and its role in repair and pathology after spinal cord injury
Gensel, J. C., & Zhang, B. (2015) · Brain Research · doi:10.1016/j.brainres.2014.12.045 · Cited by 792
Macrophage polarization and diabetic wound healing
Louiselle, A. E., Niemiec, S. M., Zgheib, C., & Liechty, K. W. (2021) · Translational research · doi:10.1016/j.trsl.2021.05.006 · Cited by 757
Macrophage polarization in pathology
Sica, A., Erreni, M., Allavena, P., & Porta, C. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1995-y · Cited by 673
Macrophage phenotypes during tissue repair
Novak, M. L., & Koh, T. J. (2013) · Journal of Leukocyte Biology · doi:10.1189/jlb.1012512 · Cited by 658
Self-citationMacrophages as a therapeutic target to promote diabetic wound healing
Sharifiaghdam, M., Shaabani, E., Majidi, R. F., Smedt, S. C. D., Braeckmans, K., & Fraire, J. C. (2022) · Molecular Therapy · doi:10.1016/j.ymthe.2022.07.016 · Cited by 606
Myofibroblast proliferation and heterogeneity are supported by macrophages during skin repair
Shook, B. A., Wasko, R. R., Rivera-Gonzalez, G. C., Salazar-Gatzimas, E., López-Giráldez, F., Dash, B. C., Muñoz-Rojas, A. R., Aultman, K. D., Zwick, R. K., Lei, V., et al. (2018) · Science · doi:10.1126/science.aar2971 · Cited by 519
Mirza, R. E., Fang, M. M., Ennis, W. J., & Koh, T. J. (2013) · Diabetes · doi:10.2337/db12-1450 · Cited by 467
Self-citationSkin Wound Healing: Normal Macrophage Function and Macrophage Dysfunction in Diabetic Wounds
Aitcheson, S. M., Frentiu, F. D., Hurn, S. E., Edwards, K. P., & Murray, R. Z. (2021) · Molecules · doi:10.3390/molecules26164917 · Cited by 457
Macrophage and Fibroblast Interactions in Biomaterial‐Mediated Fibrosis
Witherel, C. E., Abebayehu, D., Barker, T. H., & Spiller, K. L. (2019) · Advanced Healthcare Materials · doi:10.1002/adhm.201801451 · Cited by 374
Deregulated immune cell recruitment orchestrated by FOXM1 impairs human diabetic wound healing
Sawaya, A. P., Stone, R. C., Brooks, S. R., Pastar, I., Jozic, I., Hasneen, K., O’Neill, K. E., Mehdizadeh, S., Head, C. R., Štrbo, N., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-18276-0 · Cited by 370
Phenotypic Transitions of Macrophages Orchestrate Tissue Repair
Novak, M. L., & Koh, T. J. (2013) · American Journal Of Pathology · doi:10.1016/j.ajpath.2013.06.034 · Cited by 370
Self-citationOsteoMacs: Key players around bone biomaterials
Miron, R. J., & Bosshardt, D. D. (2015) · Biomaterials · doi:10.1016/j.biomaterials.2015.12.017 · Cited by 327
Mirza, R. E., Fang, M. M., Weinheimer-Haus, E. M., Ennis, W. J., & Koh, T. J. (2014) · Diabetes · doi:10.2337/db13-0927 · Cited by 319
“For mouse wounds, healing was assessed on day 10 postinjury using our previously published assays of granulation tissue formation and re-epithelialization using hematoxylin-eosin–stained cryosections (4,14).”
BackgroundMethodInfluentialSelf-citationMacrophage-based therapeutic strategies in regenerative medicine
Spiller, K. L., & Koh, T. J. (2017) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2017.05.010 · Cited by 310
Self-citationXu, N., Gao, Y., Li, Z., Chen, Y., Liu, M., Jia, J., Zeng, R., Luo, G., Li, J., & Yu, Y. (2023) · Chemical Engineering Journal · doi:10.1016/j.cej.2023.143173 · Cited by 249
Mohammadi, A., Blesso, C. N., Barreto, G. E., Banach, M., Majeed, M. A., & Sahebkar, A. (2018) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2018.12.005 · Cited by 229
Disclosure of the culprits: macrophages-versatile regulators of wound healing.
Sindrilaru, A., & Scharffetter-Kochanek, K. (2013) · Advances in Wound Care · doi:10.1089/wound.2012.0407 · Cited by 223
Transcriptome analysis of IL-10-stimulated (M2c) macrophages by next-generation sequencing
Lurier, E. B., Dalton, D., Dampier, W., Raman, P., Nassiri, S., Ferraro, N. M., Rajagopalan, R., Sarmady, M., & Spiller, K. L. (2017) · Immunobiology · doi:10.1016/j.imbio.2017.02.006 · Cited by 222
Liu, D., Yang, P., Gao, M., Yu, T., Shi, Y., Zhang, M., Yao, M., Liu, Y., & Zhang, X. (2019) · Clinical Science · doi:10.1042/cs20180600 · Cited by 221
Kimball, A., Schaller, M. A., Joshi, A., Davis, F. M., denDekker, A. D., Boniakowski, A. E., Bermick, J., Obi, A. T., Moore, B. B., Henke, P. K., et al. (2018) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.118.310703 · Cited by 216
Macrophage activation and skeletal muscle healing following traumatic injury
Novak, M. L., Weinheimer-Haus, E. M., & Koh, T. J. (2013) · The Journal of Pathology · doi:10.1002/path.4301 · Cited by 208
Self-citationThe Monocyte to Macrophage Transition in the Murine Sterile Wound
Crane, M. J., Daley, J. M., van Houtte, O., Brancato, S. K., Henry, W. L., & Albina, J. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0086660 · Cited by 188
CD301b+ Macrophages Are Essential for Effective Skin Wound Healing
Shook, B. A., Xiao, E., Kumamoto, Y., Iwasaki, A., & Horsley, V. (2016) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2016.05.107 · Cited by 186
Macrophages are necessary for epimorphic regeneration in African spiny mice
Simkin, J., Gawriluk, T. R., Gensel, J. C., & Seifert, A. W. (2017) · eLife · doi:10.7554/elife.24623 · Cited by 197
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Brown, B. N., Sicari, B. M., & Badylak, S. F. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00510 · Cited by 195
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Shi, Z., Yao, C., Shui, Y., Li, S., & Yan, H. (2023) · Frontiers in Physiology · doi:10.3389/fphys.2023.1284981 · Cited by 204
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Wolf, S., Melvin, W. J., & Gallagher, K. A. (2021) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2021.06.013 · Cited by 190
Yu, T., Gao, M., Yang, P., Liu, D., Wang, D., Song, F., Zhang, X., & Liu, Y. (2018) · Journal of Cellular Physiology · doi:10.1002/jcp.27185 · Cited by 186
Macrophage PPARγ and impaired wound healing in type 2 diabetes
Mirza, R. E., Fang, M. M., Novak, M. L., Urao, N., Sui, A., Ennis, W. J., & Koh, T. J. (2015) · The Journal of Pathology · doi:10.1002/path.4548 · Cited by 177
“Mouse wound healing was assessed, on day 10 post-injury, by our published assays of external wound closure, using digital images of the external wound surface and re-epithelialization and granulation tissue formation, with haematoxylin and eosin (H&E)-stained cryosections [16,20,21].”
BackgroundMethodResultInfluentialSelf-citationPalmitate and Lipopolysaccharide Trigger Synergistic Ceramide Production in Primary Macrophages
Schilling, J. D., Machkovech, H. M., Li, H., Sidhu, R., Fujiwara, H., Weber, K., Ory, D. S., & Schaffer, J. E. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m112.419978 · Cited by 186
Kimball, A., Davis, F. M., denDekker, A. D., Joshi, A., Schaller, M. A., Bermick, J., Xing, X., Burant, C., Obi, A. T., Nysz, D., et al. (2019) · Immunity · doi:10.1016/j.immuni.2019.06.015 · Cited by 172
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Shah, A., & Amini‐Nik, S. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18051068 · Cited by 184
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Self-citationWound Administration of M2-Polarized Macrophages Does Not Improve Murine Cutaneous Healing Responses
Jetten, N., Roumans, N., Gijbels, M. J., Romano, A., Post, M. J., de Winther, M. P. J., van der Hulst, R. R. W. J., & Xanthoulea, S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0102994 · Cited by 162
Huang, S., Wu, C., Chiu, M., Wu, C., Chang, Y., Chen, G., & Lan, C.-C. E. (2019) · Journal of Dermatological Science · doi:10.1016/j.jdermsci.2019.11.004 · Cited by 163
Okizaki, S.-I., Ito, Y., Hosono, K., Oba, K., Ohkubo, H., Amano, H., Shichiri, M., & Majima, M. (2014) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2014.10.020 · Cited by 150
Bannon, P., Wood, S., Restivo, T., Campbell, L., Hardman, M., & Mace, K. (2013) · Disease Models & Mechanisms · doi:10.1242/dmm.012237 · Cited by 154
Wermuth, P. J., & Jiménez, S. A. (2015) · Clinical and Translational Medicine · doi:10.1186/s40169-015-0047-4 · Cited by 141
Hauck, S., Zager, P., Halfter, N., Wandel, E., Torregrossa, M., Kakpenova, A., Rother, S., Ordieres, M. D., Räthel, S., Berg, A., et al. (2021) · Bioactive Materials · doi:10.1016/j.bioactmat.2021.04.026 · Cited by 142
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Weber, K., & Schilling, J. D. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m113.531202 · Cited by 139
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Schultze, J. L., Schmieder, A., & Goerdt, S. (2015) · Seminars in Immunology · doi:10.1016/j.smim.2015.07.003 · Cited by 134
Franz, S., Ertel, A., Engel, K. M., Simon, J. C., & Saalbach, A. (2022) · Theranostics · doi:10.7150/thno.67174 · Cited by 129
Monaghan, M. G., Borah, R., Thomsen, C., & Browne, S. (2023) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2023.115120 · Cited by 131
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Self-citationWeinheimer-Haus, E. M., Mirza, R. E., & Koh, T. J. (2015) · PLoS ONE · doi:10.1371/journal.pone.0119106 · Cited by 95
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Das, A., Abas, M., Biswas, N., Banerjee, P., Ghosh, N., Rawat, A. K., Khanna, S., Roy, S., & Sen, C. K. (2019) · Scientific Reports · doi:10.1038/s41598-019-49435-z · Cited by 95
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Yang, Z., Lin, S., Feng, W., Liu, Y., Song, Z., Pan, G., Zhang, Y., Dai, X., Ding, X., Chen, L., et al. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.999179 · Cited by 92
Dai, J., Zhang, X., Li, L., Chen, H., & Chai, Y. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000480367 · Cited by 87
Xu, M., Su, T., Jin, X., Li, Y., Yao, Y., Liu, K., Chen, K., Lu, F., & He, Y. (2022) · Acta Biomaterialia · doi:10.1016/j.actbio.2022.08.015 · Cited by 86
Shen, T. N.-Y., Kanazawa, S., Kado, M., Okada, K., Luo, L., Hayashi, A., Mizuno, H., & Tanaka, R. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178232 · Cited by 89
Zhang, Q.-Z., Yu, W., Lee, S., Xu, Q.-L., Naji, A., & Le, A. (2015) · Journal of Bone and Mineral Research · doi:10.1002/jbmr.2577 · Cited by 79
Cardiolipotoxicity, Inflammation, and Arrhythmias: Role for Interleukin-6 Molecular Mechanisms
Alì, A., Boutjdir, M., & Aromolaran, A. S. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2018.01866 · Cited by 86
Grosick, R. L., Alvarado-Vazquez, P. A., Messersmith, A., & Romero-Sandoval, E. A. (2018) · Journal of Pain Research · doi:10.2147/jpr.s164493 · Cited by 82
Topical application of substance P promotes wound healing in streptozotocin-induced diabetic rats
Kant, V., Kumar, D., Kumar, D., Prasad, R., Gopal, A., Pathak, N. N., Kumar, P., & Tandan, S. K. (2015) · Cytokine · doi:10.1016/j.cyto.2014.12.015 · Cited by 79
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Clayton, S. M., Shafikhani, S. H., & Soulika, A. M. (2024) · Advances in Wound Care · doi:10.1089/wound.2023.0149 · Cited by 86
Zhang, Q., Oh, J.-H., Park, C. H., Baek, J., Ryoo, H., & Woo, K. M. (2017) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.6b15815 · Cited by 77
Kerstan, A., Dieter, K., Niebergall‐Roth, E., Klingele, S., Jünger, M., Hasslacher, C., Daeschlein, G., Stemler, L., Meyer-Pannwitt, U., Schubert, K. A., et al. (2022) · Stem Cell Research & Therapy · doi:10.1186/s13287-022-03156-9 · Cited by 76
Wlaschek, M., Singh, K., Sindrilaru, A., Crisan, D., & Scharffetter-Kochanek, K. (2019) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.09.036 · Cited by 76
Lee, R. S. B., Hamlet, S. M., Moon, H., & Ivanovski, S. (2020) · Biomaterials · doi:10.1016/j.biomaterials.2020.120464 · Cited by 75
Bhadauriya, P., Mamtani, H., Ashfaq, M., Raghav, A., Teotia, A. K., Kumar, A., & Verma, N. (2018) · ACS Applied Bio Materials · doi:10.1021/acsabm.8b00018 · Cited by 70
O’Brien, E. M., & Spiller, K. L. (2021) · Journal of Leukocyte Biology · doi:10.1002/jlb.3a0520-338r · Cited by 75
Selective M2 Macrophage Depletion Leads to Prolonged Inflammation in Surgical Wounds
Klinkert, K., Whelan, D., Clover, A. J. P., Leblond, A., Kumar, A. H. S., & Caplice, N. M. (2017) · European Surgical Research · doi:10.1159/000451078 · Cited by 67
In Vivo Imaging Reveals a Pioneer Wave of Monocyte Recruitment into Mouse Skin Wounds
Rodero, M., Licata, F., Poupel, L., Hamon, P., Khosrotehrani, K., Combadière, C., & Boissonnas, A. (2014) · PLoS ONE · doi:10.1371/journal.pone.0108212 · Cited by 55
Okizaki, S.-I., Ito, Y., Hosono, K., Oba, K., Ohkubo, H., Kojo, K., Nishizawa, N., Shibuya, M., Shichiri, M., & Majima, M. (2016) · American Journal Of Pathology · doi:10.1016/j.ajpath.2016.02.014 · Cited by 64
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Zhou, L., Liu, F., You, J., Zhou, B., Guo, W., Qu, W., Ren, X., & Gao, G. (2023) · Advanced Healthcare Materials · doi:10.1002/adhm.202303460 · Cited by 62
Ding, Y., Ding, X., Zhang, H., Li, S., Yang, P., & Tan, Q. (2022) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2022/9687925 · Cited by 66
Wounds under diabetic milieu: The role of immune cellar components and signaling pathways
Lin, S., Wang, Q., Huang, X., Feng, J., Wang, Y., Shao, T., Deng, X., Cao, Y., Chen, X.-H., Zhou, M., et al. (2022) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2022.114052 · Cited by 62
Barman, P. K., Urao, N., & Koh, T. J. (2019) · The Journal of Pathology · doi:10.1002/path.5330 · Cited by 61
Self-citationTeh, H. X., Phang, S. J., Looi, M. L., Kuppusamy, U. R., & Arumugam, B. (2023) · Life Sciences · doi:10.1016/j.lfs.2023.122228 · Cited by 63
Liu, Y., Zhang, X., Yang, L., Zhou, S., Li, Y., Shen, Y., Lu, S., Zhou, J., & Liu, Y. (2023) · Phytomedicine · doi:10.1016/j.phymed.2023.154892 · Cited by 62
The Role of Adipocytes in Tissue Regeneration and Stem Cell Niches
Shook, B. A., Rivera-Gonzalez, G. C., Ebmeier, S., Grisotti, G., Zwick, R. K., & Horsley, V. (2016) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev-cellbio-111315-125426 · Cited by 59
Metadata
- Authors
- Mirza, R., & Koh, T. J.
- Affiliations
- University of Illinois Chicago (US)
- Corresponding author
- Koh, Timothy J.
- ORCID
- Koh, Timothy J.
- Venue
- Cytokine
- Publisher
- Elsevier BV
- Published
- 2011-11
- Volume
- 56
- Issue
- 2
- Pages
- 256-264
- ISSN
- 1043-4666 (ISSN-L)
- OpenAlex
- W2057864569
- Semantic Scholar
- 1f48248e2a91668cf09529b853c24fad07f4f0ba
- Cited by
- 342
- References
- 41
- Citations by year
- 2026: 20 · 2025: 32 · 2024: 29 · 2023: 35 · 2022: 30 · 2021: 23 · 2020: 29 · 2019: 25 · 2018: 21 · 2017: 21 · 2016: 18 · 2015: 21 · 2014: 17 · 2013: 10 · 2012: 10
- FWCI
- 11.99
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Cytokine (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of Illinois at Chicago
- Topics
- Health Sciences › Medicine › Surgery › Wound Healing and Treatments
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetic Foot Ulcer Assessment and Management
- Life Sciences › Immunology and Microbiology › Immunology › Immune cells in cancer
- Keywords
- diabetic wound healing, macrophage polarization, inflammatory macrophages, alternative macrophage activation, db/db mice, IL-1β, MMP-9, inducible nitric oxide synthase, CD206, CD36, insulin-like growth factor I, TGF-β1, vascular endothelial growth factor, angiogenesis, granulation tissue, collagen deposition, interferon-gamma, IL-10
- MeSH terms
- Animals, Base Sequence, Diabetes Mellitus, Experimental, Enzyme-Linked Immunosorbent Assay, Flow Cytometry, Macrophages, Monocytes, Wound Healing, Wounds and Injuries, Immunophenotyping, Polymerase Chain Reaction, DNA Primers, Mice
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