Impaired healing of nitrogen mustard wounds in CXCR2 null mice
Open accessAbstract
To examine the significance of chemokine activation of CXCR2 in wound healing after chemical burn, cutaneous injury was created by topical application of nitrogen mustard on CXCR2 wild type (+/+), heterozygous (+/–), and knockout (–/–) mice. Wounds were analyzed histologically for neutrophil and monocyte infiltration and for reepithelialization at postwound days 4, 7, and 10. Neutrophil recruitment to the wound site was reduced through postwound day 7 in CXCR2 –/– mice as indicated by myeloperoxidase assay and by visual quantitation. Because there is always concern that mice with targeted deletion of a specific receptor may undergo developmental adaptations to offset the loss of the receptor, we also accessed chemical wound repair in the presence of a small molecule antagonist of CXCR2. Dietary supplementation with a CXCR2 antagonist (SB‐265610) during the wound repair process also markedly delayed healing parameters in CXCR2 +/+ mice, even greater than treatment with glucocorticoids. These parallel studies further establish that mice deficient in CXCR2 function exhibit delayed cutaneous wound healing that may be primarily linked to impaired neutrophil recruitment after chemical burn with nitrogen mustard. Thus, there may be a potential therapeutic benefit of treating nitrogen mustard‐induced skin lesions with agonists of CXCR2 to facilitate the wound repair process. (WOUND REP REG 2003;11:213–219)
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CXCR2−/− mice display impaired neutrophil recruitment and delayed wound healing.
“CXCR2−/− mice display impaired neutrophil recruitment and delayed wound healing.47,48”
From The Innate Immune System in Acute and Chronic Wounds (2016) · cites this paper as [48]
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Cites
Chemokines in cutaneous wound healing
Gillitzer, R., & Goebeler, M. (2001) · Journal of Leukocyte Biology · doi:10.1189/jlb.69.4.513 · Cited by 943 · see citing works
Hübner, G., Brauchle, M. A., Smola, H., Madlener, M., Fässler, R., & Werner, S. (1996) · Cytokine · doi:10.1006/cyto.1996.0074 · Cited by 499 · see citing works
White, J. R., Lee, J. M., Young, P. R., Hertzberg, R., Jurewicz, A. J., Chaikin, M. A., Widdowson, K. L., Foley, J. J., Martin, L. D., Griswold, D. E., et al. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.17.10095 · Cited by 434 · see citing works
Self-citationDelayed Wound Healing in CXCR2 Knockout Mice
Devalaraja, R. M., Nanney, L. B., Qian, Q., Du, J., Yu, Y., Devalaraja, M. N., & Richmond, A. (2000) · Journal of Investigative Dermatology · doi:10.1046/j.1523-1747.2000.00034.x · Cited by 429 · see citing works
Self-citationWound Healing in MIP-1α−/− and MCP-1−/− Mice
Low, Q., Drugea, I. A., Duffner, L. A., Quinn, D. G., Cook, D. N., Rollins, B. J., Kovacs, E. J., & DiPietro, L. A. (2001) · American Journal Of Pathology · doi:10.1016/s0002-9440(10)61717-8 · Cited by 300 · see citing works
MIP-1alpha as a critical macrophage chemoattractant in murine wound repair.
DiPietro, L. A., Burdick, M., Low, Q., Kunkel, S. L., & Strieter, R. M. (1998) · Journal of Clinical Investigation · doi:10.1172/jci1020 · Cited by 273 · see citing works
Cytokine-regulated proteases in autoimmune diseases
Opdenakker, G., & Damme, J. V. (1994) · Immunology Today · doi:10.1016/0167-5699(94)90151-1 · Cited by 208 · see citing works
Agents of chemical warfare: Sulfur mustard
Borak, J., & Sidell, F. R. (1992) · Annals of Emergency Medicine · doi:10.1016/s0196-0644(05)80892-3 · Cited by 183 · see citing works
Myeloperoxidase as a Biomarker of Skin Irritation and Inflammation
Trush, M. A., Egner, P. A., & Kensler, T. W. (1994) · Food and Chemical Toxicology · doi:10.1016/0278-6915(94)90175-9 · Cited by 146 · see citing works
Interleukin‐8 levels and activity in delayed‐healing human thermal wounds
Iocono, J. A., Colleran, K. R., Remick, D. G., Gillespie, B. W., Ehrlich, H. P., & Garner, W. L. (2000) · Wound Repair and Regeneration · doi:10.1046/j.1524-475x.2000.00216.x · Cited by 107 · see citing works
Luster, A. D., Cardiff, R. D., MacLean, J. A., Crowe, K., & Granstein, R. D. (1998) · PubMed · Cited by 105 · see citing works
Feugate, J. E., Li, Q., Wong, L., & Martins‐Green, M. M. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200103062 · Cited by 88 · see citing works
Smith, K. J., Smith, W. J., Hamilton, T. A., Skelton, H. G., Graham, J. S., Okerberg, C. V., Moeller, R. B., & Hackley, B. E. (1998) · American Journal of Dermatopathology · doi:10.1097/00000372-199802000-00005 · Cited by 88 · see citing works
Nanney, L. B., Mueller, S. G., Bueno, R., Peiper, S. C., & Richmond, A. J. (1995) · Europe PMC (PubMed Central) · Cited by 82 · see citing works
Self-citationEstève, É., Bagot, M., Joly, P., Souteyrand, P., Beylot-Barry, M., Vaillant, L., Delaunay, M. M., Avril, M.-F., Laroche, L., Grange, F., et al. (1999) · Archives of Dermatology · doi:10.1001/archderm.135.11.1349 · Cited by 46 · see citing works
Petrali, J. P., Oglesby, S. B., Hamilton, T. A., & Mills, K. R. (1993) · PubMed · Cited by 32 · see citing works
Poszepczynska, E., Martinvalet, D., Bouloc, A., Echchakir, H., Wechsler, J., Bécherel, P., Boumsell, L., Bensussan, A., & Bagot, M. (2001) · British Journal of Dermatology · doi:10.1046/j.1365-2133.2001.04203.x · Cited by 23 · see citing works
Reddy, V. B., Ramsay, D. L., Garcia, J. A., & Kamino, H. (1996) · American Journal of Dermatopathology · doi:10.1097/00000372-199602000-00003 · Cited by 20 · see citing works
Evaluation of a 1-h exposure time to mechlorethamine in patients undergoing topical treatment
Foulc, P., Evrard, V., Dalac, S., Guillot, B., Delaunay, M. M., Verret, J.-L., & Dréno, B. (2002) · British Journal of Dermatology · doi:10.1046/j.1365-2133.2002.04802.x · Cited by 18 · see citing works
Flagged first, then by citations
Research works printed but not linked: 2
- [8]Leeson TS, Leeson CR, Paparo AA. General histological principles and primary tissues text/atlas of histology. Philadelphia: Saunders; 1988. pp. 206–7. [Google Scholar]
- [13]Nanney L, Mueller S, Bueno R, Peiper S, Richmond A. Distributions of MGSA/GRO and the IL-8 receptor B in wound repair. Am J Path. 1995;147:1248–60. [PMC free article] [PubMed] [Google Scholar]
Cited by
Sorted by citations
Role of the CXCL8-CXCR1/2 Axis in Cancer and Inflammatory Diseases
Ha, H., Debnath, B., & Neamati, N. (2017) · Theranostics · doi:10.7150/thno.15625 · Cited by 788 · see citing works
“However, they do exhibit impaired wound healing and angiogenesis, increased susceptibility to pathogens, and decreased pathogen clearance due to reduced neutrophil recruitment [109-117].”
Neutrophil chemoattractant receptors in health and disease: Double-edged swords
Metzemaekers, M., Gouwy, M., & Proost, P. (2020) · Cellular & Molecular Immunology · doi:10.1038/s41423-020-0412-0 · Cited by 570 · see citing works
“Furthermore, the absence of CXCR2 was associated with delayed experimental cutaneous wound healing in mice, supporting the notion that neutrophils are critically involved in tissue repair.(166) Neutrophils within the tumor microenvironment may be classified into protumoral and antitumoral phenotypes,(167) and the cont…”
BackgroundCellular and Molecular Dynamics in the Foreign Body Reaction
Luttikhuizen, D. T., Harmsen, M. C., & Luyn, M. J. A. V. (2006) · Tissue Engineering · doi:10.1089/ten.2006.12.1955 · Cited by 396 · see citing works
“56,57 During the onset of inflammation, the levels of CXCL-1 and CXCL-2 rise significantly.”
Chemokines and Chemokine Receptors: Standing at the Crossroads of Immunobiology and Neurobiology
Ransohoff, R. M. (2009) · Immunity · doi:10.1016/j.immuni.2009.09.010 · Cited by 372 · see citing works
“The exceptional versatility of CXCR2 is best shown through its implication in cutaneous wound healing (Devalaraja et al., 2000; Milatovic et al., 2003).”
BackgroundPotential roles and targeted therapy of the CXCLs/CXCR2 axis in cancer and inflammatory diseases
Cheng, Y., Ma, X., Wei, Y.-Q., & Wei, X. (2019) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2019.01.005 · Cited by 343 · see citing works
The Innate Immune System in Acute and Chronic Wounds
MacLeod, A. S., & Mansbridge, J. N. (2016) · Advances in Wound Care · doi:10.1089/wound.2014.0608 · Cited by 289 · see citing works
“CXCR2 - / mice display impaired neutrophil recruitment and delayed wound healing.(47,48) These chemokines are characterized by the sequence ELR at their N-terminus.”
BackgroundThe chemokine system – a major regulator of angiogenesis in health and disease
ROSENKILDE, M. M., & Schwartz, T. W. (2004) · Apmis · doi:10.1111/j.1600-0463.2004.apm11207-0808.x · Cited by 256 · see citing works
“The importance of CXCR2 (and its interaction with ELR CXC chemokines) in wound healing is supported by the notion that CXCR2-deficient mice – or wildtype mice treated with the CXCR2-specific nonpeptide antagonist SB225002 (66, 67) – have delayed wound healing (46, 66, 68).”
BackgroundThe wound healing, chronic fibrosis, and cancer progression triad
Rybinski, B., Franco‐Barraza, J., & Cukierman, E. (2014) · Physiological Genomics · doi:10.1152/physiolgenomics.00158.2013 · Cited by 255 · see citing works
CXCR2 antagonists for the treatment of pulmonary disease
Chapman, R. W., Phillips, J. E., Hipkin, R. W., Curran, A. K., Lundell, D., & Fine, J. S. (2009) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2008.10.005 · Cited by 214 · see citing works
Bizzarri, C., Beccari, A. R., Bertini, R., Cavicchia, M. R., Giorgini, S., & Allegretti, M. (2006) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2006.04.002 · Cited by 206 · see citing works
Raghuwanshi, S. K., Su, Y., Singh, V., Haynes, K., Richmond, A. J., & Richardson, R. M. (2012) · The Journal of Immunology · doi:10.4049/jimmunol.1201114 · Cited by 150 · see citing works
“Myeloperoxidase (MPO) activity was assayed, as described previously (37, 38).”
MethodSelf-citationChemokine Regulation of Neutrophil Infiltration of Skin Wounds
Su, Y., & Richmond, A. J. (2014) · Advances in Wound Care · doi:10.1089/wound.2014.0559 · Cited by 139 · see citing works
“Such deficiency in healing was also confirmed in CXCR2 - / - mice with a chemical-induced skin injury model.(36) Specifically, CXCR2 deficiency associates with a spectrum of dysfunctions of cell migration and proliferation in keratinocytes and endothelial cells leading to delayed reepithelialization, granulation tissu…”
BackgroundSelf-citationElevated Local Senescence in Diabetic Wound Healing Is Linked to Pathological Repair via CXCR2
Wilkinson, H. N., Clowes, C., Banyard, K. L., Matteuci, P., Mace, K. A., & Hardman, M. J. (2019) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2019.01.005 · Cited by 139 · see citing works
Zaja‐Milatovic, S., & Richmond, A. J. (2008) · PubMed · doi:10.14670/hh-23.1399 · Cited by 126 · see citing works
“, 1998) also showed delayed wound healing (Milatovic et al., 2003).”
BackgroundMethodInfluentialSelf-citationSemple, B. D., Bye, N., Ziebell, J. M., & Morganti-Kossmann, M. C. (2010) · Neurobiology of Disease · doi:10.1016/j.nbd.2010.06.015 · Cited by 113 · see citing works
“This is consistent with previous findings of intermediate myeloperoxidase activity and neutrophil infiltration in Cxcr2+/− mice following excision wounds (Devalaraja et al., 2000) and chemical burns (Milatovic et al., 2003).”
Models for the study of skin wound healing. The role of Nrf2 and NF-κB
Ambrožová, N., Jitka Ulrichová, A., & Galandáková, A. (2017) · Biomedical Papers · doi:10.5507/bp.2016.063 · Cited by 112 · see citing works
Modarresi, M., Farahpour, M., & Baradaran, B. (2018) · InflammoPharmacology · doi:10.1007/s10787-018-0510-0 · Cited by 87 · see citing works
Altered CXCR2 Signaling in β-Arrestin-2-Deficient Mouse Models
Su, Y., Raghuwanshi, S. K., Yu, Y., Nanney, L. B., Richardson, R. M., & Richmond, A. J. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.175.8.5396 · Cited by 90 · see citing works
“MPO activity was assayed as described previously (36, 39).”
BackgroundMethodSelf-citationDepletion of β-Arrestin-2 Promotes Tumor Growth and Angiogenesis in a Murine Model of Lung Cancer
Raghuwanshi, S. K., Nasser, M. W., Chen, X. L., Strieter, R. M., & Richardson, R. M. (2008) · The Journal of Immunology · doi:10.4049/jimmunol.180.8.5699 · Cited by 71 · see citing works
“CXCR2deficient mice as well as mice treated with CXCR2-neutralizing Ab displayed impaired angiogenesis, diminished healing in excisional and chemical burn wounds, and tumor development (18, 22, 37, 38).”
BackgroundPoly I:C induces collective migration of HaCaT keratinocytes via IL-8
Takada, K., Komine‐Aizawa, S., Hirohata, N., Trinh, Q. D., Nishina, A., Kimura, H., & Hayakawa, S. (2017) · BMC Immunology · doi:10.1186/s12865-017-0202-3 · Cited by 51 · see citing works
“In null CXCR2 mice, which lack a functional IL-8 receptor, wound healing is delayed [41, 42], and in human skin, topical administration of IL-8 increased the length of the reepithelialized area [32].”
Future therapeutic treatment of COPD: struggle between oxidants and cytokines.
de Boer, W. I., Yao, H., & Rahman, I. (2007) · PubMed Central · Cited by 49 · see citing works
Molecular mechanisms in chronic obstructive pulmonary disease
de Boer, W. I., Alagappan, V. K. T., & SHARMA, H. S. (2007) · Cell Biochemistry and Biophysics · doi:10.1385/cbb:47:1:131 · Cited by 42 · see citing works
“In vivo, impaired CXCR2 expression in mice resulted in delayed skin wound repair as compared to wild-type mice, which could not be restored by exogenous CXCL8 application (61).”
BackgroundJain, A., Tewari‐Singh, N., Inturi, S., Orlicky, D. J., White, C. W., & Agarwal, R. (2013) · Experimental and Toxicologic Pathology · doi:10.1016/j.etp.2013.11.005 · Cited by 38 · see citing works
“A detailed study on the pathological effects of NM and the evaluation of these effects as biomarkers has not been reported (Anumolu et al., 2011, Gunhan et al., 2004, Milatovic et al., 2003, Wormser et al., 1997).”
BackgroundPerspectives for cytokine antagonist therapy in COPD
de Boer, W. I. (2005) · Drug Discovery Today · doi:10.1016/s1359-6446(04)03300-8 · Cited by 38 · see citing works
Bieren, J. E., Volpe, B., Sutherland, D. B., Bürgi, J., Verbeek, J. S., Marsland, B. J., Urban, J. F., & Harris, N. L. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1004778 · Cited by 37 · see citing works
“This included the CXCR2 ligands Cxcl2 and Cxcl3, which have been implicated in cutaneous wound healing [21,22].”
BackgroundMethodInfluentialHerlea‐Pana, O., Yao, L., Heuser‐Baker, J., Wang, Q., Wang, Q., Georgescu, C., Zou, M., & Barlic‐Dicen, J. (2015) · Cardiovascular Research · doi:10.1093/cvr/cvv111 · Cited by 35 · see citing works
“CXCR2 expression is important in angiogenesis(17) and in wound healing.(18) CXCR2 is also known to promote plaque formation.”
BackgroundVitamin D3 and deconvoluting a rash
Ernst, M. K., Evans, S. T., Techner, J., Rothbaum, R. M., Christensen, L., Onay, V., Biyashev, D., Demczuk, M. M., Nguyen, C. V., Honda, K. S., et al. (2023) · JCI Insight · doi:10.1172/jci.insight.163789 · Cited by 32 · see citing works
“While specific markers of an exaggerated response to NM skin injury have not been previously identified in humans, our results are consistent with past data implicating neutrophilic, monocytic, and T cell– mediated processes in exaggerated responses to topical chemotherapeutics (8, 25, 34).”
CXCR2 deficient mice display macrophage-dependent exaggerated acute inflammatory responses
Dyer, D. P., Pallas, K. J., Medina‐Ruiz, L., Schuette, F., Wilson, G. J., & Graham, G. J. (2017) · Scientific Reports · doi:10.1038/srep42681 · Cited by 31 · see citing works
The chemokine KC regulates HGF-stimulated epithelial cell morphogenesis
Ueland, J. M., Gwira, J. A., Liu, Z., & Cantley, L. G. (2004) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00289.2003 · Cited by 26 · see citing works
“In addition, repair of wounded epithelium in these knockout mice is delayed compared with control mice (8, 26).”
BackgroundDiverging Mechanisms of Activation of Chemokine Receptors Revealed by Novel Chemokine Agonists
Sarmiento, J., Shumate, C. K., Suetomi, K., Ravindran, A., Villegas, L., Rajarathnam, K., & Navarro, J. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027967 · Cited by 24 · see citing works
“Whereas the functional role of CXCR2 can be examined by using CXCR2-deficient mice [3] or the administration of CXCR2 selective agonists (CXCL1-3 and CXCL57) or non-peptide CXCR2 antagonists [4], elucidating the role of CXCR1 in vivo is hampered by the lack of specific CXCR1 agonists and antagonists, and because mice…”
BackgroundTewari‐Singh, N., Jain, A., Inturi, S., White, C. W., & Agarwal, R. (2013) · PLoS ONE · doi:10.1371/journal.pone.0067557 · Cited by 21 · see citing works
“Therefore, we focused our studies on NM, a bi-functional alkylating agent like SM, whose effects are reported to be similar to SM [25,26] and few studies are published with NM in human skin explants and mouse skin [25–30].”
BackgroundExpression of cytokines and chemokines in mouse skin treated with sulfur mustard
Chang, Y.-C., Soriano, M., Hahn, R. A., Casillas, R. P., Gordon, M. K., Laskin, J. D., & Gerecke, D. R. (2018) · Toxicology and Applied Pharmacology · doi:10.1016/j.taap.2018.06.008 · Cited by 21 · see citing works
“These findings are in accord with earlier studies demonstrating increased numbers of MPO neutrophils by 7 days in mouse skin exposed to mustards (Milatovic et al., 2003; Tewari-Singh et al., 2009; Jain et al., 2014; Tewari-Singh et al., 2014a; Tewari-Singh et al., 2014b; Mouret et al., 2015).”
Cellular and Molecular Dynamics in the Foreign Body Reaction
Luttikhuizen, D. T., Harmsen, M. C., & van Luyn, M. J. A. (2006) · Tissue Engineering · doi:10.1089/ten.2006.12.ft-126 · Cited by 21 · see citing works
Liu, Z., Yang, Y., Zhou, F., Ma, K., Lin, X., Yan, S.-Q., Yu, G., & Chen, W. (2021) · Veterinary Research · doi:10.1186/s13567-021-00937-7 · Cited by 20 · see citing works
“Cxcr2−/− mice show impaired neutrophil recruitment and delayed wound healing [37, 38].”
BackgroundBischoff, D. S., Sakamoto, T., Ishida, K., Makhijani, N. S., Gruber, H. E., & Yamaguchi, D. T. (2010) · Bone · doi:10.1016/j.bone.2010.09.026 · Cited by 17 · see citing works
“Wounds generated by nitrogen mustard produced a robust inflammatory response in WT mice, while similar wounds in mCXCR−/− mice did not result in a significant neutrophilic inflammatory infiltrate [5].”
BackgroundChen, K., Wei, Y., Alter, A., Sharp, G. C., & Braley‐Mullen, H. (2005) · Journal of Leukocyte Biology · doi:10.1189/jlb.0205102 · Cited by 16 · see citing works
“Studies have demonstrated the critical role of PMN infiltration in tissue damage, wound healing, and development of fibrosis [1, 10, 23, 25, 37, 38].”
BackgroundChoudhury, S., Dhoke, N. R., Chawla, S., & Das, A. (2024) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-023-05057-3 · Cited by 15 · see citing works
“Furthermore, delayed or impaired wound healing was reported in CXCR2 deficient mice due to the lack of neutrophil and monocyte recruitment and reduced secretion of IL-1β at the wound site [41, 42].”
BackgroundCXCR 2 modulates bone marrow vascular repair and haematopoietic recovery post‐transplant
Hale, S. J. M., Hale, A., Zhang, Y., Sweeney, D., Fisher, N., van der Garde, M., Grabowska, R., Pepperell, E. E., Channon, K. M., Martin‐Rendon, E., et al. (2015) · British Journal of Haematology · doi:10.1111/bjh.13335 · Cited by 10 · see citing works
“It has also been demonstrated by others that Cxcr2 / mice have impaired skin revascularization following injury (Devalaraja et al, 2000; Milatovic et al, 2003).”
BackgroundDefining the timing of 25(OH)D rescue following nitrogen mustard exposure
Das, L. M., Binko, A. M., Traylor, Z. P., Duesler, L., & Lu, K. Q. (2017) · Cutaneous and Ocular Toxicology · doi:10.1080/15569527.2017.1355315 · Cited by 7 · see citing works
Inflammation in Wound Repair: Role and Function of Inflammation in Wound Repair
MacLeod, A. S., & Kwock, J. T. (2017) · Wiley eBooks · doi:10.1002/9781119282518.ch14 · Cited by 7 · see citing works
Transgenic and gene knock-out techniques and burn research
Wolf, S. E., & Woodside, K. J. (2004) · Journal of Surgical Research · doi:10.1016/j.jss.2004.06.001 · Cited by 5 · see citing works
Chemokine receptors (version 2020.5) in the IUPHAR/BPS Guide to Pharmacology Database
Bachelerie, F., Ben‐Baruch, A., Burkhardt, A. M., Charo, I. F., Combadière, C., Förster, R., Farber, J. M., Graham, G. J., Hills, R., Horuk, R., et al. (2020) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f14/2020.5 · Cited by 3 · see citing works
Chemokine receptors in GtoPdb v.2023.1
Bachelerie, F., Ben‐Baruch, A., Burkhardt, A. M., Charo, I. F., Combadière, C., Förster, R., Farber, J. M., Graham, G. J., Hills, R., Horuk, R., et al. (2023) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f14/2023.1 · Cited by 2 · see citing works
IL-8 receptor antagonist: basic research and clinical utility
White, J. R., & Sarau, H. M. (2007) · Birkhäuser Basel eBooks · doi:10.1007/978-3-7643-7437-2_7 · Cited by 2 · see citing works
“Since then several other compounds from this series have been reported, all are CXCR2 selective, and have been shown to have activity in several animal models including LPS-induced lung neutrophilia [29], acute and chronic models of arthritis [30], wound healing [ 31 ] and lung inflammation [32].”
BackgroundSelf-citationChemokine receptors (version 2019.5) in the IUPHAR/BPS Guide to Pharmacology Database
Bachelerie, F., Ben‐Baruch, A., Charo, I. F., Combadière, C., Förster, R., Farber, J. M., Graham, G. J., Hills, R., Horuk, R., Locati, M., et al. (2019) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f14/2019.5 · Cited by 2 · see citing works
Klopsfenstein, N., Hibbs, K., Blackman, A., & Serezani, C. H. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.10.02.510554 · Cited by 2 · see citing works
Kimura, M., & Sugaya, N. (2012) · Journal of Allergy & Therapy · doi:10.4172/2155-6121.s5-005 · Cited by 1 · see citing works
“Because neutrophil infiltration responding to inflammatory stimulation is markedly reduced in neutrophil-chemokine receptordeficient mice [23,24], chemokines such as KC and MIP-2 are considered to be involved in the migration of neutrophils.”
BackgroundChemokine receptors (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database
Bachelerie, F., Ben‐Baruch, A., Charo, I. F., Combadière, C., Förster, R., Farber, J. M., Graham, G. J., Hills, R., Horuk, R., Locati, M., et al. (2019) · IUPHAR/BPS Guide to Pharmacology CITE · doi:10.2218/gtopdb/f14/2019.4 · Cited by 1 · see citing works
Sarmiento, J., Shumate, C. K., Suetomi, K., Ravindran, A., Villegas, L. N., Rajarathnam, K., & Navarro, J. (2012) · PLoS ONE · doi:10.1371/annotation/81d01b33-4eb2-459c-b600-0094d9f2d194 · Cited by 1 · see citing works
Yu, Y., Su, Y., Opalenik, S. R., Sobolik-Delmaire, T., Neel, N. F., Zaja‐Milatovic, S., Short, S. P., Sai, J., & Richmond, A. J. (2008) · Journal of Leukocyte Biology · doi:10.1189/jlb.0807544 · Cited by 1 · see citing works
“The CXCR2 ligands (CXCL1, CXCL5, CXCL8) are present in keratinocytes and neutrophils and can be released upon wounding to stimulate the woundhealing response [4, 25, 28].”
BackgroundSelf-citationRegulation of cellar cytokine production and NF-κB pathway by ginseng and ginsenosides
Zhou, Y. (2016) · RMIT Research Repository (RMIT University Library) · doi:10.25439/rmt.27581643
Liu, Z., Yang, Y.-J., Zhou, F.-H., Ma, K., Lin, X.-Q., Yan, S.-Q., Gao, Y., & Chen, W. (2021) · Figshare · doi:10.6084/m9.figshare.14623084
Liu, Z., Yang, Y.-J., Zhou, F.-H., Ma, K., Lin, X.-Q., Yan, S.-Q., Gao, Y., & Chen, W. (2021) · Figshare · doi:10.6084/m9.figshare.14623078
Liu, Z., Yang, Y.-J., Zhou, F.-H., Ma, K., Lin, X.-Q., Yan, S.-Q., Gao, Y., & Chen, W. (2021) · Figshare · doi:10.6084/m9.figshare.14623087
Liu, Z., Yang, Y.-J., Zhou, F.-H., Ma, K., Lin, X.-Q., Yan, S.-Q., Gao, Y., & Chen, W. (2021) · Figshare · doi:10.6084/m9.figshare.14623081
- Authors
- Milatovic, S., Nanney, L. B., Yu, Y., White, J. R., & Richmond, A.
- Affiliations
- Vanderbilt University (US)
- Centre for Cancer Biology (AU)
- GlaxoSmithKline (United States) (US)
- United States Department of Veterans Affairs (US)
- Corresponding author
- Richmond, Ann
- Venue
- Wound Repair and Regeneration
- Publisher
- Wiley
- Published
- 2003-05
- Volume
- 11
- Issue
- 3
- Pages
- 213-219
- ISSN
- 1067-1927 (ISSN-L)
- 1524-475X
- PMC
- PMC2667443
- OpenAlex
- W2035570125
- Cited by
- 55
- References
- 19
- Citations by year
- 2024: 1 · 2023: 2 · 2022: 1 · 2021: 5 · 2020: 2 · 2019: 4 · 2018: 2 · 2017: 6 · 2016: 1 · 2015: 4 · 2014: 2 · 2013: 2 · 2012: 3
- FWCI
- 2.87
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Wound Repair and Regeneration (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- U.S. Department of Veterans Affairs (IK6 BX005225)
- National Cancer Institute (R01CA034590)
- National Institute of General Medical Sciences (GM 40437, R01GM040437)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (P30AR041943, P30-AR41943)
- Topics
- Health Sciences › Medicine › Rehabilitation › Wound Healing and Treatments
- Health Sciences › Medicine › Oncology › Chemokine receptors and signaling
- Health Sciences › Medicine › Epidemiology › Burn Injury Management and Outcomes
- Keywords
- CXCR2, wound healing, nitrogen mustard, skin wounds, neutrophil recruitment, chemokines, CXCR2 antagonist, re-epithelialization, chemical burns, glucocorticoids
- MeSH terms
- Animals, Burns, Chemical, Mechlorethamine, Mice, Inbred BALB C, Peroxidase, Neutrophils, Prednisolone, Time Factors, Wound Healing, Wounds and Injuries, Polymerase Chain Reaction, Mice, Knockout, Receptors, Chemokine, Receptors, Interleukin-8B, Mice
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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.
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