Interleukin-8 is able to promote pro-inflammatory activity of human monocytes (macrophages)
- Авторлар: Meniailo M.E1,2, Malashchenko V.V1, Shmarov V.A1, Gazatova N.D1, Melashchenko O.B1, Goncharov A.G1, Seledtsova G.V3, Seledtsov V.I2
-
Мекемелер:
- Immanuel Kant Baltic Federal University
- Russian Research Center of Medical Rehabilitation and Balneotherapy
- Scientific Research Institute of Clinical Immunology
- Шығарылым: Том 13, № 1 (2018)
- Беттер: 65-69
- Бөлім: Articles
- ##submission.dateSubmitted##: 05.01.2023
- ##submission.datePublished##: 15.03.2018
- URL: https://genescells.ru/2313-1829/article/view/120726
- DOI: https://doi.org/10.23868/201805007
- ID: 120726
Дәйексөз келтіру
Аннотация
Негізгі сөздер
Толық мәтін
![Рұқсат жабық](https://genescells.ru/lib/pkp/templates/images/icons/text_lock.png)
Авторлар туралы
M. Meniailo
Immanuel Kant Baltic Federal University; Russian Research Center of Medical Rehabilitation and Balneotherapy
Email: max89me@yandex.ru
VV. Malashchenko
Immanuel Kant Baltic Federal University
VA. Shmarov
Immanuel Kant Baltic Federal University
N. Gazatova
Immanuel Kant Baltic Federal University
O. Melashchenko
Immanuel Kant Baltic Federal University
A. Goncharov
Immanuel Kant Baltic Federal University
G. Seledtsova
Scientific Research Institute of Clinical Immunology
V. Seledtsov
Russian Research Center of Medical Rehabilitation and Balneotherapy
Әдебиет тізімі
- Brat D.J., Bellail A.C., Van Meir E.G. The role of interleukin-8 and its receptors in gliomagenesis and tumoral angiogenesis. Neurooncol. 2005; 7(2): 122-33.
- Меняйло М.Е., Малащенко В.В., Шмаров В.А. и соавт. Прямое влияние интерлейкина-8 на активацию Т-клеток. Российский иммунологический журнал 2016; 10(2): 174-8.
- Bickel M. The role of interleukin-8 in inflammation and mechanisms of regulation. J. periodontol. 1993; 64(5): 456-60.
- Hedges J.C., Singer C.A., Gerthoffer W.T. Mitogen-activated protein kinases regulate cytokine gene expression in human airway myocytes. Am. J. Respir. Cell. Mol. Biol. 2000; 23(1): 86-94.
- Casilli F., Bianchini A., Gloaguen I. et al. Inhibition of interleukin-8 (CXCL8/IL-8) responses by repertaxin, a new inhibitor of the chemokine receptors CXCR1 and CxCR2. Biochem. Pharmacol. 2005; 69(3): 385-94.
- Segerer S., Henger A., Schmid H. et al. Expression of the chemokine receptor CXCR1 in human glomerular diseases. Kidney int. 2006; 69(10): 1765-73.
- Nasser M.W., Raghuwanshi S.K., Grant D.J. et al. Differential activation and regulation of CXCR1 and CXCR2 by CXCL8 monomer and dimer. J. Immunol. 2009; 183(5): 3425-32.
- de Oliveira S., Rosowski, E.E., Huttenlocher A. Neutrophil migration in infection and wound repair: going forward in reverse. Nat. Rev. Immunol. 2016; 16(6): 378-91.
- Jacobs J.P., Ortiz-Lopez A., Campbell J.J. et al. Deficiency of CXCR2, but not other chemokine receptors, attenuates autoantibody-mediated arthritis in a murine model. Arthritis Rheum. 2010; 62(7): 1921-32.
- Ziegler-Heitbrock L., Ancuta P., Crowe S. et al. Nomenclature of monocytes and dendritic cells in blood. Blood 2010; 116(16): e74-e80.
- Italiani P., Boraschi D. From monocytes to M1/M2 macrophages: phenotypical vs. functional differentiation. Front. immunol. 2014; 5: 514.
- Allaire M.A., Tanne B., Côte S.C. et al. Prostaglandin E2 does not modulate CCR7 expression and functionality after differentiation of blood monocytes into macrophages. Int. J. Inflam. 2013; 2013: 918016.
- Yang J., Zhang L., Yu C. et al. Monocyte and macrophage differentiation: circulation inflammatory monocyte as biomarker for inflammatory diseases. Biomark. Res. 2014; 2(1): 1.
- Kitchens R. Role of CD14 in cellular recognition of bacterial lipopolysaccharides. Chem. Immunol. 2000; 74: 61-82.
- Martinez F.O., Gordon S. The M1 and M2 paradigm of macrophage activation: time for reassessment. F1000 Prime Rep. 2014; 6(13.10): 12703.
- Tau G., Rothman P. Biologic functions of the IFN-y receptors. Allergy 1999; 54(12): 1233-51.
- Nelms K., Keegan A.D., Zamorano J. et al. The IL-4 receptor: signaling mechanisms and biologic functions. Annu. Rev. Immunol. 1999; 17(1): 701-38.
- Junt T., Scandella E., Foster R. et al. Impact of CCR7 on priming and distribution of antiviral effector and memory CTL. J. Immunol. 2004; 173(11): 6684-93.
- Duque G.A., Descoteaux A. Macrophage cytokines: involvement in immunity and infectious diseases. Front. Immunol. 2014; 5: 491
- Rey-Giraud F., Hafner M., Ries C.H. In vitro generation of monocyte-derived macrophages under serum-free conditions improves their tumor promoting functions. PloS one 2012; 7(8): e42656.
- Seledtsov V.I., Seledtsova G.V. A balance between tissue-destructive and tissue-protective immunities: a role of toll-like receptors in regulation of adaptive immunity. Immunobiology 2012; 217(4): 430-5.
- Muraille E., Leo O., Moser M. TH1/TH2 paradigm extended: macrophage polarization as an unappreciated pathogen-driven escape mechanism? Front. Immunol. 2014; 5, 603.
- Zhang Z., Song L., Maurer K. et al. Monocyte polarization: the relationship of genome-wide changes in H4 acetylation with polarization. Genes Immun. 2011; 12(6): 445-56.
- Gesser B., Deleuran B., Lund M. et al. Interleukin-8 induces its own production in CD4+ T lymphocytes: a process regulated by interleukin 10. Biochem. Biophys. Res. Commun. 1995; 210(3): 660-9.
- Brown K.D., Claudio E. The roles of the classical and alternative nuclear factor-kappa B pathways: potential implications for autoimmunity and rheumatoid arthritis. Arthritis Res. Ther. 2008; 10(4): 212.
Қосымша файлдар
![](/img/style/loading.gif)