Adverse effects of CXCR2 deficiency in mice reared under non-gnotobiotic conditions.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
30 10 2024
Historique:
received: 22 01 2024
accepted: 07 10 2024
medline: 31 10 2024
pubmed: 31 10 2024
entrez: 31 10 2024
Statut: epublish

Résumé

The family of pro-inflammatory and pro-angiogenic chemokines including Interleukin-8 (IL-8, aka CXCL8) and its homologues (CXCL1,2,3,5,6, and 7) exhibit promiscuous binding and activation of several G-protein-coupled receptors (i.e., CXCR2, CXCR1, and the atypical chemokine receptor (ACKR1)). A high proportion of their biological activity is attributed to CXCR2 activation, thus many CXCR2 inhibitors are in clinical trials for several chronic diseases. However, CXCR2 inhibition is often only investigated acutely in these trials or in Cxcr2

Identifiants

pubmed: 39478033
doi: 10.1038/s41598-024-75532-9
pii: 10.1038/s41598-024-75532-9
doi:

Substances chimiques

Receptors, Interleukin-8B 0
Cxcr2 protein, mouse 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

26159

Subventions

Organisme : International Retinal Research Foundation
ID : GF02527
Organisme : NEI NIH HHS
ID : K08 EY029006
Pays : United States
Organisme : Vanderbilt Diabetes Research and Training Center, Vanderbilt University Medical Center
ID : DK020593
Organisme : Research to Prevent Blindness
ID : Unrestricted Grant

Informations de copyright

© 2024. The Author(s).

Références

Semple, B. D., Kossmann, T. & Morganti-Kossmann, M. C. Role of chemokines in CNS health and pathology: A focus on the CCL2/CCR2 and CXCL8/CXCR2 networks. J. Cereb. Blood Flow Metab. 30, 459–473. https://doi.org/10.1038/jcbfm.2009.240 (2010).
doi: 10.1038/jcbfm.2009.240 pubmed: 19904283
Wuyts, A. et al. Differential usage of the CXC chemokine receptors 1 and 2 by interleukin-8, granulocyte chemotactic protein-2 and epithelial-cell-derived neutrophil attractant-78. Eur. J. Biochem. 255, 67–73. https://doi.org/10.1046/j.1432-1327.1998.2550067.x (1998).
doi: 10.1046/j.1432-1327.1998.2550067.x pubmed: 9692902
Fan, X. et al. Murine CXCR1 is a functional receptor for GCP-2/CXCL6 and interleukin-8/CXCL8. J. Biol. Chem. 282, 11658–11666. https://doi.org/10.1074/jbc.M607705200 (2007).
doi: 10.1074/jbc.M607705200 pubmed: 17197447
Pruenster, M. et al. The Duffy antigen receptor for chemokines transports chemokines and supports their promigratory activity. Nat. Immunol. 10, 101–108. https://doi.org/10.1038/ni.1675 (2009).
doi: 10.1038/ni.1675 pubmed: 19060902
Mollica Poeta, V., Massara, M., Capucetti, A. & Bonecchi, R. Chemokines and chemokine receptors: New targets for cancer immunotherapy. Front. Immunol. 10, 379. https://doi.org/10.3389/fimmu.2019.00379 (2019).
doi: 10.3389/fimmu.2019.00379 pubmed: 30894861
Yin, C. et al. CXCL5 activates CXCR2 in nociceptive sensory neurons to drive joint pain and inflammation in experimental gouty arthritis. Nat. Commun. 15, 3263. https://doi.org/10.1038/s41467-024-47640-7 (2024).
doi: 10.1038/s41467-024-47640-7 pubmed: 38627393
Al-Alwan, L. A. et al. Differential roles of CXCL2 and CXCL3 and their receptors in regulating normal and asthmatic airway smooth muscle cell migration. J. Immunol. 191, 2731–2741. https://doi.org/10.4049/jimmunol.1203421 (2013).
doi: 10.4049/jimmunol.1203421 pubmed: 23904157
Coelho, F. M. et al. The chemokine receptors CXCR1/CXCR2 modulate antigen-induced arthritis by regulating adhesion of neutrophils to the synovial microvasculature. Arthritis Rheum. 58, 2329–2337. https://doi.org/10.1002/art.23622 (2008).
doi: 10.1002/art.23622 pubmed: 18668539
Henrot, P., Prevel, R., Berger, P. & Dupin, I. Chemokines in COPD: From implication to therapeutic use. Int. J. Mol. Sci. 20, https://doi.org/10.3390/ijms20112785 (2019).
Wang, S. et al. CXCL1-CXCR2 signalling mediates hypertensive retinopathy by inducing macrophage infiltration. Redox Biol. 56, 102438. https://doi.org/10.1016/j.redox.2022.102438 (2022).
doi: 10.1016/j.redox.2022.102438 pubmed: 35981418
Horuk, R. Chemokine receptor antagonists: Overcoming developmental hurdles. Nat. Rev. Drug Discov. 8, 23–33. https://doi.org/10.1038/nrd2734 (2009).
doi: 10.1038/nrd2734 pubmed: 19079127
Kerstetter, A. E., Padovani-Claudio, D. A., Bai, L. & Miller, R. H. Inhibition of CXCR2 signaling promotes recovery in models of multiple sclerosis. Exp. Neurol. 220, 44–56. https://doi.org/10.1016/j.expneurol.2009.07.010 (2009).
doi: 10.1016/j.expneurol.2009.07.010 pubmed: 19616545
Liu, L. et al. CXCR2-positive neutrophils are essential for cuprizone-induced demyelination: Relevance to multiple sclerosis. Nat. Neurosci. 13, 319–326. https://doi.org/10.1038/nn.2491 (2010).
doi: 10.1038/nn.2491 pubmed: 20154684
Padovani-Claudio, D. A., Liu, L., Ransohoff, R. M. & Miller, R. H. Alterations in the oligodendrocyte lineage, myelin, and white matter in adult mice lacking the chemokine receptor CXCR2. Glia 54, 471–483. https://doi.org/10.1002/glia.20383 (2006).
doi: 10.1002/glia.20383 pubmed: 16886211
Gavard, J. et al. A role for a CXCR2/phosphatidylinositol 3-kinase gamma signaling axis in acute and chronic vascular permeability. Mol. Cell. Biol. 29, 2469–2480. https://doi.org/10.1128/MCB.01304-08 (2009).
doi: 10.1128/MCB.01304-08 pubmed: 19255141
Qu, Y., Zhou, F. & Xu, X. Y. Selective non-peptide CXCR2 antagonist SB225002 inhibits choroidal neovascularization in rat model. Zhonghua Yan Ke Za Zhi 45, 742–745 (2009).
pubmed: 20021889
Lazaar, A. L. et al. CXCR2 antagonist for patients with chronic obstructive pulmonary disease with chronic mucus hypersecretion: A phase 2b trial. Respir. Res. 21, 149. https://doi.org/10.1186/s12931-020-01401-4 (2020).
doi: 10.1186/s12931-020-01401-4 pubmed: 32532258
O’Byrne, P. M. et al. Efficacy and safety of a CXCR2 antagonist, AZD5069, in patients with uncontrolled persistent asthma: A randomised, double-blind, placebo-controlled trial. Lancet Respir. Med. 4, 797–806. https://doi.org/10.1016/S2213-2600(16)30227-2 (2016).
doi: 10.1016/S2213-2600(16)30227-2 pubmed: 27574788
Roberts, G. et al. Randomized, double-blind, placebo-controlled study of the safety, tolerability, and clinical effect of danirixin in adults with acute, uncomplicated influenza. Open Forum Infect. Dis. 6, ofz072. https://doi.org/10.1093/ofid/ofz072 (2019).
Sordi, V. et al. Post hoc analysis of a randomized, double-blind, prospective trial evaluating a CXCR1/2 inhibitor in new-onset type 1 diabetes: Endo-metabolic features at baseline identify a subgroup of responders. Front. Endocrinol. 14, 1175640. https://doi.org/10.3389/fendo.2023.1175640 (2023).
doi: 10.3389/fendo.2023.1175640
Dabir, S. S. et al. Differential systemic gene expression profile in patients with diabetic macular edema: Responders versus nonresponders to standard treatment. Indian J. Ophthalmol. 62, 66–73. https://doi.org/10.4103/0301-4738.126186 (2014).
doi: 10.4103/0301-4738.126186 pubmed: 24492504
Knickelbein, J. E., Chan, C. C., Sen, H. N., Ferris, F. L. & Nussenblatt, R. B. Inflammatory mechanisms of age-related macular degeneration. Int. Ophthalmol. Clin. 55, 63–78. https://doi.org/10.1097/IIO.0000000000000073 (2015).
doi: 10.1097/IIO.0000000000000073 pubmed: 26035762
Wagner, B. D. et al. Association of systemic inflammatory factors with progression to advanced age-related macular degeneration. Ophthalmic Epidemiol. 29, 139–148. https://doi.org/10.1080/09286586.2021.1910314 (2022).
doi: 10.1080/09286586.2021.1910314 pubmed: 33827374
Elner, S. G. et al. Interferon-induced protein 10 and interleukin 8. C-X-C chemokines present in proliferative diabetic retinopathy. Arch Ophthalmol. 116, 1597–1601. https://doi.org/10.1001/archopht.116.12.1597 (1998).
Goczalik, I. et al. Expression of CXCL8, CXCR1, and CXCR2 in neurons and glial cells of the human and rabbit retina. Invest. Ophthalmol. Vis. Sci. 49, 4578–4589. https://doi.org/10.1167/iovs.08-1887 (2008).
doi: 10.1167/iovs.08-1887 pubmed: 18552386
Addison, C. L. et al. The CXC chemokine receptor 2, CXCR2, is the putative receptor for ELR + CXC chemokine-induced angiogenic activity. J. Immunol. 165, 5269–5277. https://doi.org/10.4049/jimmunol.165.9.5269 (2000).
doi: 10.4049/jimmunol.165.9.5269 pubmed: 11046061
Han, X. et al. CXCR2 expression on granulocyte and macrophage progenitors under tumor conditions contributes to mo-MDSC generation via SAP18/ERK/STAT3. Cell Death Dis. 10, 598. https://doi.org/10.1038/s41419-019-1837-1 (2019).
doi: 10.1038/s41419-019-1837-1 pubmed: 31395859
Katoh, H. et al. CXCR2-expressing myeloid-derived suppressor cells are essential to promote colitis-associated tumorigenesis. Cancer Cell 24, 631–644. https://doi.org/10.1016/j.ccr.2013.10.009 (2013).
doi: 10.1016/j.ccr.2013.10.009 pubmed: 24229710
Matsuo, Y. et al. CXC-chemokine/CXCR2 biological axis promotes angiogenesis in vitro and in vivo in pancreatic cancer. Int. J. Cancer 125, 1027–1037. https://doi.org/10.1002/ijc.24383 (2009).
doi: 10.1002/ijc.24383 pubmed: 19431209
Urbantat, R. M. et al. The CXCL2/IL8/CXCR2 pathway is relevant for brain tumor malignancy and endothelial cell function. Int. J. Mol. Sci. 22, https://doi.org/10.3390/ijms22052634 (2021).
Wente, M. N. et al. Blockade of the chemokine receptor CXCR2 inhibits pancreatic cancer cell-induced angiogenesis. Cancer Lett. 241, 221–227. https://doi.org/10.1016/j.canlet.2005.10.041 (2006).
doi: 10.1016/j.canlet.2005.10.041 pubmed: 16458421
Cacalano, G. et al. Neutrophil and B cell expansion in mice that lack the murine IL-8 receptor homolog. Science 265, 682–684. https://doi.org/10.1126/science.8036519 (1994).
doi: 10.1126/science.8036519 pubmed: 8036519
Sinclair, A. et al. CXCR2 and CXCL4 regulate survival and self-renewal of hematopoietic stem/progenitor cells. Blood 128, 371–383. https://doi.org/10.1182/blood-2015-08-661785 (2016).
doi: 10.1182/blood-2015-08-661785 pubmed: 27222476 pmcid: 4991087
Padovani-Claudio, D. A. Functional analyses of the chemokine receptor Cxcr2 in the normal and demyelinated adult central nervous system (2006).
Padovani-Claudio, D. A., Palmer, S. A., Beatty, N. J. & Penn, J. S. Chemokine modulation as a potential therapy for retinal angiogenesis. Investig. Ophthalmol. Vis. Sci. 60, 2721–2721 (2019).
Broxmeyer, H. E. et al. Involvement of Interleukin (IL) 8 receptor in negative regulation of myeloid progenitor cells in vivo: Evidence from mice lacking the murine IL-8 receptor homologue. J. Exp. Med. 184, 1825–1832. https://doi.org/10.1084/jem.184.5.1825 (1996).
doi: 10.1084/jem.184.5.1825 pubmed: 8920870
Petreaca, M. L., Yao, M., Liu, Y., Defea, K. & Martins-Green, M. Transactivation of vascular endothelial growth factor receptor-2 by interleukin-8 (IL-8/CXCL8) is required for IL-8/CXCL8-induced endothelial permeability. Mol. Biol. Cell 18, 5014–5023. https://doi.org/10.1091/mbc.e07-01-0004 (2007).
doi: 10.1091/mbc.e07-01-0004 pubmed: 17928406
Fruttiger, M. et al. PDGF mediates a neuron-astrocyte interaction in the developing retina. Neuron 17, 1117–1131. https://doi.org/10.1016/s0896-6273(00)80244-5 (1996).
doi: 10.1016/s0896-6273(00)80244-5 pubmed: 8982160
Jiang, S. et al. The role of CXCL1/CXCR2 axis in neurological diseases. Int. Immunopharmacol. 120, 110330. https://doi.org/10.1016/j.intimp.2023.110330 (2023).
doi: 10.1016/j.intimp.2023.110330 pubmed: 37247498
Zhang, Z. Y. et al. Promotion of axon regeneration and protection on injured retinal ganglion cells by rCXCL2. Inflamm. Regen. 43, 31. https://doi.org/10.1186/s41232-023-00283-5 (2023).
doi: 10.1186/s41232-023-00283-5 pubmed: 37340465
Liu, Y. F. et al. CXCL5/CXCR2 modulates inflammation-mediated neural repair after optic nerve injury. Exp. Neurol. 341, 113711. https://doi.org/10.1016/j.expneurol.2021.113711 (2021).
doi: 10.1016/j.expneurol.2021.113711 pubmed: 33785307
Rodriguez, A. R., de Sevilla Muller, L. P. & Brecha, N. C. The RNA binding protein RBPMS is a selective marker of ganglion cells in the mammalian retina. J. Comp. Neurol. 522, 1411–1443. https://doi.org/10.1002/cne.23521 (2014).
doi: 10.1002/cne.23521 pubmed: 24318667
Andoh, M., Ikegaya, Y. & Koyama, R. Microglia in animal models of autism spectrum disorders. Prog. Mol. Biol. Transl. Sci. 173, 239–273. https://doi.org/10.1016/bs.pmbts.2020.04.012 (2020).
doi: 10.1016/bs.pmbts.2020.04.012 pubmed: 32711812
Shuster, D. E., Kehrli, M. E. Jr. & Ackermann, M. R. Neutrophilia in mice that lack the murine IL-8 receptor homolog. Science 269, 1590–1591. https://doi.org/10.1126/science.7667641 (1995).
doi: 10.1126/science.7667641 pubmed: 7667641
Singh, S., Varney, M. & Singh, R. K. Host CXCR2-dependent regulation of melanoma growth, angiogenesis, and experimental lung metastasis. Cancer Res. 69, 411–415. https://doi.org/10.1158/0008-5472.CAN-08-3378 (2009).
doi: 10.1158/0008-5472.CAN-08-3378 pubmed: 19147552
Choe, D. et al. High-fat diet-induced obese effects of adipocyte-specific CXCR2 conditional knockout in the peritoneal tumor microenvironment of ovarian cancer. Cancers 13, https://doi.org/10.3390/cancers13195033 (2021).
Canela-Xandri, O., Rawlik, K. & Tenesa, A. An atlas of genetic associations in UK Biobank. Nat. Genet. 50, 1593–1599. https://doi.org/10.1038/s41588-018-0248-z (2018).
doi: 10.1038/s41588-018-0248-z pubmed: 30349118 pmcid: 6707814
Pirinen, M., Donnelly, P. & Spencer, C. C. A. Efficient computation with a linear mixed model on large-scale data sets with applications to genetic studies. Ann. Appl. Stat. 7, 369–390. https://doi.org/10.1214/12-Aoas586 (2013).
doi: 10.1214/12-Aoas586
Padovani-Claudio, D. A. et al. CXCR2 inhibitors: Friends or foes?. Investig. Ophthalmol. Vis. Sci. 65, 1734–1734 (2024).
Wong, T. Y. et al. Quantitative retinal venular caliber and risk of cardiovascular disease in older persons: The cardiovascular health study. Arch. Intern. Med. 166, 2388–2394. https://doi.org/10.1001/archinte.166.21.2388 (2006).
doi: 10.1001/archinte.166.21.2388 pubmed: 17130394
Tamai, K. et al. Lipid hydroperoxide stimulates leukocyte-endothelium interaction in the retinal microcirculation. Exp. Eye Res. 75, 69–75. https://doi.org/10.1006/exer.2002.1178 (2002).
doi: 10.1006/exer.2002.1178 pubmed: 12123638
Kanno, K., Hirata, Y., Imai, T. & Marumo, F. Induction of nitric oxide synthase gene by interleukin in vascular smooth muscle cells. Hypertension 22, 34–39. https://doi.org/10.1161/01.hyp.22.1.34 (1993).
doi: 10.1161/01.hyp.22.1.34 pubmed: 7686532
Velten, I. M., Horn, F. K., Korth, M. & Velten, K. The b-wave of the dark adapted flash electroretinogram in patients with advanced asymmetrical glaucoma and normal subjects. Br. J. Ophthalmol. 85, 403–409. https://doi.org/10.1136/bjo.85.4.403 (2001).
doi: 10.1136/bjo.85.4.403 pubmed: 11264127
Dong, C. J. & Hare, W. A. Contribution to the kinetics and amplitude of the electroretinogram b-wave by third-order retinal neurons in the rabbit retina. Vis. Res. 40, 579–589. https://doi.org/10.1016/s0042-6989(99)00203-5 (2000).
doi: 10.1016/s0042-6989(99)00203-5 pubmed: 10824262
Wang, J. J. et al. Cytotoxic effect of interleukin-8 in retinal ganglion cells and its possible mechanisms. Int. J. Ophthalmol. 11, 1277–1283. https://doi.org/10.18240/ijo.2018.08.05 (2018).
doi: 10.18240/ijo.2018.08.05 pubmed: 30140629
Holden, J. M., Wareham, L. K. & Calkins, D. J. Retinal astrocyte morphology predicts integration of vascular and neuronal architecture. Front. Neurosci. 17, 1244679. https://doi.org/10.3389/fnins.2023.1244679 (2023).
doi: 10.3389/fnins.2023.1244679 pubmed: 37621717
Delobel, P., Ginter, B., Rubio, E., Balabanian, K. & Lazennec, G. CXCR2 intrinsically drives the maturation and function of neutrophils in mice. Front. Immunol. 13, 1005551. https://doi.org/10.3389/fimmu.2022.1005551 (2022).
doi: 10.3389/fimmu.2022.1005551 pubmed: 36311783
Zhao, Y. et al. Duffy antigen receptor for chemokines mediates chemokine endocytosis through a macropinocytosis-like process in endothelial cells. PloS ONE 6, e29624. https://doi.org/10.1371/journal.pone.0029624 (2011).
doi: 10.1371/journal.pone.0029624 pubmed: 22216333
Permanyer, M., Bosnjak, B. & Forster, R. Dual role for atypical chemokine receptor 1 in myeloid cell hematopoiesis and distribution. Cell. Mol. Immunol. 15, 399–401. https://doi.org/10.1038/cmi.2017.79 (2018).
doi: 10.1038/cmi.2017.79 pubmed: 29532789
Horuk, R. The duffy antigen receptor for chemokines DARC/ACKR1. Front. Immunol. 6, 279. https://doi.org/10.3389/fimmu.2015.00279 (2015).
doi: 10.3389/fimmu.2015.00279 pubmed: 26097477
Devalaraja, R. M. et al. Delayed wound healing in CXCR2 knockout mice. J. Investig. Dermatol. 115, 234–244. https://doi.org/10.1046/j.1523-1747.2000.00034.x (2000).
doi: 10.1046/j.1523-1747.2000.00034.x pubmed: 10951241
Hang, L., Frendeus, B., Godaly, G. & Svanborg, C. Interleukin-8 receptor knockout mice have subepithelial neutrophil entrapment and renal scarring following acute pyelonephritis. J. Infectious Di. 182, 1738–1748. https://doi.org/10.1086/317599 (2000).
doi: 10.1086/317599
Moore, M. W., Cacalano, G., Wood, W. I. & Bailish, E. Response. Science 269, 1591. https://doi.org/10.1126/science.269.5230.1591 (1995).
doi: 10.1126/science.269.5230.1591 pubmed: 17789451
Cardona, A. E. et al. Scavenging roles of chemokine receptors: Chemokine receptor deficiency is associated with increased levels of ligand in circulation and tissues. Blood 112, 256–263. https://doi.org/10.1182/blood-2007-10-118497 (2008).
doi: 10.1182/blood-2007-10-118497 pubmed: 18347198 pmcid: 2442740
Serdar, M. et al. Involvement of CXCL1/CXCR2 during microglia activation following inflammation-sensitized hypoxic-ischemic brain injury in neonatal rats. Front. Neurol. 11, 540878. https://doi.org/10.3389/fneur.2020.540878 (2020).
doi: 10.3389/fneur.2020.540878 pubmed: 33123073
Monickaraj, F., Acosta, G., Cabrera, A. P. & Das, A. Transcriptomic profiling reveals chemokine CXCL1 as a mediator for neutrophil recruitment associated with blood-retinal barrier alteration in diabetic retinopathy. Diabetes 72, 781–794. https://doi.org/10.2337/db22-0619 (2023).
doi: 10.2337/db22-0619 pubmed: 36930735
Michael, B. D. et al. Astrocyte- and neuron-derived CXCL1 drives neutrophil transmigration and blood-brain barrier permeability in viral encephalitis. Cell Rep. 32, 108150. https://doi.org/10.1016/j.celrep.2020.108150 (2020).
doi: 10.1016/j.celrep.2020.108150 pubmed: 32937134
Wu, F. et al. CXCR2 is essential for cerebral endothelial activation and leukocyte recruitment during neuroinflammation. J. Neuroinflammation 12, 98. https://doi.org/10.1186/s12974-015-0316-6 (2015).
doi: 10.1186/s12974-015-0316-6 pubmed: 25990934
Loetscher, P., Seitz, M., Clark-Lewis, I., Baggiolini, M. & Moser, B. Both interleukin-8 receptors independently mediate chemotaxis. Jurkat cells transfected with IL-8R1 or IL-8R2 migrate in response to IL-8, GRO alpha and NAP-2. FEBS Lett. 341, 187–192. https://doi.org/10.1016/0014-5793(94)80454-0 (1994).
doi: 10.1016/0014-5793(94)80454-0 pubmed: 8137938
Girbl, T. et al. Distinct compartmentalization of the chemokines CXCL1 and CXCL2 and the atypical receptor ACKR1 determine discrete stages of neutrophil diapedesis. Immunity 49, 1062-1076 e1066. https://doi.org/10.1016/j.immuni.2018.09.018 (2018).
doi: 10.1016/j.immuni.2018.09.018 pubmed: 30446388
Nesper, P. L. & Fawzi, A. A. Perfusion deficits in diabetes without retinopathy localize to the perivenular deep capillaries near the fovea on OCT angiography. Ophthalmol. Sci. 4, 100482. https://doi.org/10.1016/j.xops.2024.100482 (2024).
doi: 10.1016/j.xops.2024.100482 pubmed: 38751454
Zozulinska, D., Majchrzak, A., Sobieska, M., Wiktorowicz, K. & Wierusz-Wysocka, B. Serum interleukin-8 level is increased in diabetic patients. Diabetologia 42, 117–118. https://doi.org/10.1007/s001250051124 (1999).
doi: 10.1007/s001250051124 pubmed: 10027590
Feng, S. et al. Levels of inflammatory cytokines IL-1beta, IL-6, IL-8, IL-17A, and TNF-alpha in aqueous humour of patients with diabetic retinopathy. J. Diabetes Res. 2018, 8546423. https://doi.org/10.1155/2018/8546423 (2018).
doi: 10.1155/2018/8546423 pubmed: 29850610
Crawford, K. S. & Volkman, B. F. Prospects for targeting ACKR1 in cancer and other diseases. Front. Immunol. 14, 1111960. https://doi.org/10.3389/fimmu.2023.1111960 (2023).
doi: 10.3389/fimmu.2023.1111960 pubmed: 37006247
Massara, M., Bonavita, O., Mantovani, A., Locati, M. & Bonecchi, R. Atypical chemokine receptors in cancer: Friends or foes?. J. Leukocyte Biol. 99, 927–933. https://doi.org/10.1189/jlb.3MR0915-431RR (2016).
doi: 10.1189/jlb.3MR0915-431RR pubmed: 26908826
Borinstein, S. C. et al. Frequency of benign neutropenia among black versus white individuals undergoing a bone marrow assessment. J. Cell. Mol. Med. 26, 3628–3635. https://doi.org/10.1111/jcmm.17346 (2022).
doi: 10.1111/jcmm.17346 pubmed: 35642720
Auer, P. L. et al. Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits. Nat. Genet. 46, 629–634. https://doi.org/10.1038/ng.2962 (2014).
doi: 10.1038/ng.2962 pubmed: 24777453 pmcid: 4050975
Heusinkveld, L. E., Majumdar, S., Gao, J. L., McDermott, D. H. & Murphy, P. M. WHIM syndrome: From pathogenesis towards personalized medicine and cure. J. Clin. Immunol. 39, 532–556. https://doi.org/10.1007/s10875-019-00665-w (2019).
doi: 10.1007/s10875-019-00665-w pubmed: 31313072
Xue, J. et al. Red cell distribution width is associated with stroke severity and unfavorable functional outcomes in ischemic stroke. Front. Neurol. 13, 938515. https://doi.org/10.3389/fneur.2022.938515 (2022).
doi: 10.3389/fneur.2022.938515 pubmed: 36438973
Zhu, N., Shu, H., Jiang, W., Wang, Y. & Zhang, S. Mean platelet volume and mean platelet volume/platelet count ratio in nonvalvular atrial fibrillation stroke and large artery atherosclerosis stroke. Medicine 99, e21044. https://doi.org/10.1097/MD.0000000000021044 (2020).
doi: 10.1097/MD.0000000000021044 pubmed: 32664115
Zheng, M., Chen, S., Zhu, Y. & Gu, X. Mean platelet volume: A new predictor of ischaemic stroke risk in patients with nonvalvular atrial fibrillation. BMC Cardiovasc. Disord. 20, 241. https://doi.org/10.1186/s12872-020-01525-x (2020).
doi: 10.1186/s12872-020-01525-x pubmed: 32434472
Mohamed, A. B., Elnady, H. M., Alhewaig, H. K., Moslem Hefny, H. & Khodery, A. The mean platelet volume and plateletcrit as predictors of short-term outcome of acute ischemic stroke. Egypt. J. Neurol. Psychiatry Neurosurg. 55, 4. https://doi.org/10.1186/s41983-018-0035-x (2019).
doi: 10.1186/s41983-018-0035-x
Feng, G. H., Li, H. P., Li, Q. L., Fu, Y. & Huang, R. B. Red blood cell distribution width and ischaemic stroke. Stroke Vasc. Neurol. 2, 172–175. https://doi.org/10.1136/svn-2017-000071 (2017).
doi: 10.1136/svn-2017-000071 pubmed: 28989807
Greisenegger, S. et al. Is elevated mean platelet volume associated with a worse outcome in patients with acute ischemic cerebrovascular events?. Stroke 35, 1688–1691. https://doi.org/10.1161/01.STR.0000130512.81212.a2 (2004).
doi: 10.1161/01.STR.0000130512.81212.a2 pubmed: 15143290
Lekoubou, A., Pelton, M., Ba, D. M. & Ssentongo, P. Racial disparities in ischemic stroke among patients with COVID-19 in the United States. J. Stroke Cerebrovasc. Dis. Off. J. Natl. Stroke Assoc. 30, 105877. https://doi.org/10.1016/j.jstrokecerebrovasdis.2021.105877 (2021).
doi: 10.1016/j.jstrokecerebrovasdis.2021.105877
Kiew, S. Y., Thomas, G. N., Thomas, A. S. & Fekrat, S. Characteristics of central retinal vein occlusion in African Americans. J. Vitreoretin. Dis. 4, 186–191. https://doi.org/10.1177/2474126419882829 (2020).
doi: 10.1177/2474126419882829 pubmed: 37007449
Graham, G. Disparities in cardiovascular disease risk in the United States. Curr. Cardiol. Rev. 11, 238–245. https://doi.org/10.2174/1573403x11666141122220003 (2015).
doi: 10.2174/1573403x11666141122220003 pubmed: 25418513
Saederup, N. et al. Selective chemokine receptor usage by central nervous system myeloid cells in CCR2-red fluorescent protein knock-in mice. PloS ONE 5, e13693. https://doi.org/10.1371/journal.pone.0013693 (2010).
doi: 10.1371/journal.pone.0013693 pubmed: 21060874
Holden, J. M. et al. Dysfunctional cGMP signaling leads to age-related retinal vascular alterations and astrocyte remodeling in mice. Int. J. Mol. Sci. 23, https://doi.org/10.3390/ijms23063066 (2022).
Masin, L. et al. A novel retinal ganglion cell quantification tool based on deep learning. Sci. Rep. 11, 702. https://doi.org/10.1038/s41598-020-80308-y (2021).
doi: 10.1038/s41598-020-80308-y pubmed: 33436866
Martin, F. J. et al. Ensembl 2023. Nucleic Acids Res 51, D933–D941. https://doi.org/10.1093/nar/gkac958 (2023).
doi: 10.1093/nar/gkac958 pubmed: 36318249

Auteurs

Maximilian J Garcia (MJ)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Monica S Morales (MS)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Tzushan S Yang (TS)

Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.

Joseph Holden (J)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Olivia L Bossardet (OL)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Samuel A Palmer (SA)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Marvarakumari Jhala (M)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Stephen Priest (S)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Neeraj Namburu (N)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Nolan Beatty (N)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Sariah E D'Empaire Salomon (SE)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Jordan Vancel (J)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Lauren K Wareham (LK)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA.

Dolly Ann Padovani-Claudio (DA)

Department of Ophthalmology and Visual Sciences, Vanderbilt Eye Institute/Vanderbilt University Medical Center, 2311 Pierce Avenue, Nashville, TN, USA. dolly.a.padovani-claudio@vumc.org.
Vanderbilt University School of Medicine, Nashville, TN, USA. dolly.a.padovani-claudio@vumc.org.

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