Distinct functional roles of amphibian (Xenopus laevis) colony-stimulating factor-1- and interleukin-34-derived macrophages

Journal of Leukocyte Biology

Volumn 98, Issue 4, 2015, Pages 641-648

  Grayfer, Leon ^a   Robert, Jacques ^a  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

Author keywords

Antimicrobial response; CSF 1; IL 34; Myelopoiesis; Ranavirus

Indexed keywords

COLONY STIMULATING FACTOR 1; INDUCIBLE NITRIC OXIDE SYNTHASE; INTERLEUKIN 34; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE; COLONY STIMULATING FACTOR RECEPTOR; INTERLEUKIN DERIVATIVE;

ADULT; ANIMAL CELL; ANTIVIRAL ACTIVITY; ARTICLE; CELL PHAGOCYTOSIS; CONTROLLED STUDY; GENE EXPRESSION; IN VITRO STUDY; IN VIVO STUDY; MACROPHAGE; NONHUMAN; PHAGOCYTE; PRIORITY JOURNAL; RANAVIRUS; XENOPUS LAEVIS; ANIMAL; CELL CULTURE; CYTOLOGY; IMMUNOLOGY;

ANIMALS; CELLS, CULTURED; INTERLEUKINS; MACROPHAGE COLONY-STIMULATING FACTOR; MACROPHAGES; RECEPTOR, MACROPHAGE COLONY-STIMULATING FACTOR; XENOPUS LAEVIS;

EID: 84943191186     PISSN: 07415400     EISSN: 19383673     Source Type: Journal    
DOI: 10.1189/jlb.4AB0315-117RR     Document Type: Article

References (40)

1. Wang, T., Hanington, P. C., Belosevic, M., Secombes, C. J. (2008) Two macrophage colony-stimulating factor genes exist in fish that differ in gene organization and are differentially expressed. J. Immunol. 181, 3310-3322
2. Pixley, F. J., Stanley, E. R. (2004) CSF-1 regulation of the wandering macrophage: complexity in action. Trends Cell Biol. 14, 628-638
3. Hanington, P. C., Wang, T., Secombes, C. J., Belosevic, M. (2007) Growth factors of lower vertebrates: characterization of goldfish (Carassius auratus L.) macrophage colony-stimulating factor-1. J. Biol. Chem. 282, 31865-31872
4. Garceau, V., Smith, J., Paton, I. R., Davey, M., Fares, M. A., Sester, D. P., Burt, D. W., Hume, D. A. (2010) Pivotal Advance: Avian colonystimulating factor 1 (CSF-1), interleukin-34 (IL-34), and CSF-1 receptor genes and gene products. J. Leukoc. Biol. 87, 753-764
5. Lichanska, A. M., Browne, C. M., Henkel, G. W., Murphy, K. M., Ostrowski, M. C., McKercher, S. R., Maki, R. A., Hume, D. A. (1999) Differentiation of the mononuclear phagocyte system during mouse embryogenesis: the role of transcription factor PU.1. Blood 94, 127-138
6. Guilbert, L. J., Stanley, E. R. (1980) Specific interaction of murine colonystimulating factor with mononuclear phagocytic cells. J. Cell Biol. 85, 153-159
7. Belosevic, M., Hanington, P. C., Barreda, D. R. (2006) Development of goldfish macrophages in vitro. Fish Shellfish Immunol. 20, 152-171
8. Droin, N., Solary, E. (2010) Editorial: CSF1R, CSF-1, and IL-34, a “menage a trois” conserved across vertebrates. J. Leukoc. Biol. 87, 745-747
9. Lin, H., Lee, E., Hestir, K., Leo, C., Huang, M., Bosch, E., Halenbeck, R., Wu, G., Zhou, A., Behrens, D., Hollenbaugh, D., Linnemann, T., Qin, M., Wong, J., Chu, K., Doberstein, S. K., Williams, L. T. (2008) Discovery of a cytokine and its receptor by functional screening of the extracellular proteome. Science 320, 807-811
10. Wei, S., Nandi, S., Chitu, V., Yeung, Y. G., Yu, W., Huang, M., Williams, L. T., Lin, H., Stanley, E. R. (2010) Functional overlap but differential expression of CSF-1 and IL-34 in their CSF-1 receptor-mediated regulation of myeloid cells. J. Leukoc. Biol. 88, 495-505
11. Zhou, D., Huang, C., Lin, Z., Zhan, S., Kong, L., Fang, C., Li, J. (2014) Macrophage polarization and function with emphasis on the evolving roles of coordinated regulation of cellular signaling pathways. Cell. Signal. 26, 192-197
12. Hamilton, T. A., Zhao, C., Pavicic, Jr., P. G., Datta, S. (2014) Myeloid colony-stimulating factors as regulators of macrophage polarization. Front. Immunol. 5, 554
13. Chinchar, V. G. (2002) Ranaviruses (family Iridoviridae): emerging coldblooded killers. Arch. Virol. 147, 447-470
14. Morales, H. D., Abramowitz, L., Gertz, J., Sowa, J., Vogel, A., Robert, J. (2010) Innate immune responses and permissiveness to ranavirus infection of peritoneal leukocytes in the frog Xenopus laevis. J. Virol. 84, 4912-4922
15. Robert, J., Abramowitz, L., Gantress, J., Morales, H. D. (2007) Xenopus laevis: a possible vector of ranavirus infection? J. Wildl. Dis. 43, 645-652
16. De Jesús Andino, F., Chen, G., Li, Z., Grayfer, L., Robert, J. (2012) Susceptibility of Xenopus laevis tadpoles to infection by the ranavirus frogvirus 3 correlates with a reduced and delayed innate immune response in comparison with adult frogs. Virology 432, 435-443
17. Grayfer, L., Robert, J. (2014) Divergent antiviral roles of amphibian (Xenopus laevis) macrophages elicited by colony-stimulating factor-1 and interleukin-34. J. Leukoc. Biol. 96, 1143-1153
18. Grayfer, L., Robert, J. (2013) Colony-stimulating factor-1-responsive macrophage precursors reside in the amphibian (Xenopus laevis) bone marrow rather than the hematopoietic subcapsular liver. J. Innate Immun. 5, 531-542
19. Grayfer, L., De Jesús Andino, F., Robert, J. (2014) The amphibian (Xenopus laevis) type I interferon response to frog virus 3: new insight into ranavirus pathogenicity. J. Virol. 88, 5766-5777
20. Paterniti, I., Galuppo, M., Mazzon, E., Impellizzeri, D., Esposito, E., Bramanti, P., Cuzzocrea, S. (2010) Protective effects of apocynin, an inhibitor of NADPH oxidase activity, in splanchnic artery occlusion and reperfusion. J. Leukoc. Biol. 88, 993-1003
21. Gordon, S., Martinez, F. O. (2010) Alternative activation of macrophages: mechanism and functions. Immunity 32, 593-604
22. Gordon, S., Taylor, P. R. (2005) Monocyte and macrophage heterogeneity. Nat. Rev. Immunol. 5, 953-964
23. Mantovani, A., Sozzani, S., Locati, M., Allavena, P., Sica, A. (2002) Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes. Trends Immunol. 23, 549-555
24. Mills, C. D. (2012) M1 and M2 macrophages: oracles of health and disease. Crit. Rev. Immunol. 32, 463-488
25. Wang, N., Liang, H., Zen, K. (2014) Molecular mechanisms that influence the macrophage M1-M2 polarization balance. Front. Immunol. 5, 614
26. Verreck, F. A., de Boer, T., Langenberg, D. M., Hoeve, M. A., Kramer, M., Vaisberg, E., Kastelein, R., Kolk, A., de Waal-Malefyt, R., Ottenhoff, T. H. (2004) Human IL-23-producing type 1 macrophages promote but IL-10- producing type 2 macrophages subvert immunity to (myco)bacteria. Proc. Natl. Acad. Sci. USA 101, 4560-4565
27. Secombes, C. J., Wang, T., Bird, S. (2011) The interleukins of fish. Dev. Comp. Immunol. 35, 1336-1345
28. Shen, Z. J., Malter, J. S. (2015) Determinants of eosinophil survival and apoptotic cell death. Apoptosis 20, 224-234
29. De Kleer, I., Willems, F., Lambrecht, B., Goriely, S. (2014) Ontogeny of myeloid cells. Front. Immunol. 5, 423
30. Chen, X. D., Turpen, J. B. (1995) Intraembryonic origin of hepatic hematopoiesis in Xenopus laevis. J. Immunol. 154, 2557-2567
31. Hadji-Azimi, I., Coosemans, V., Canicatti, C. (1987) Atlas of adult Xenopus laevis laevis hematology. Dev. Comp. Immunol. 11, 807-874
32. Hadji-Azimi, I., Coosemans, V., Canicatti, C. (1990) B-Lymphocyte populations in Xenopus laevis. Dev. Comp. Immunol. 14, 69-84
33. Nogawa-Kosaka, N., Sugai, T., Nagasawa, K., Tanizaki, Y., Meguro, M., Aizawa, Y., Maekawa, S., Adachi, M., Kuroki, R., Kato, T. (2011) Identification of erythroid progenitors induced by erythropoietic activity in Xenopus laevis. J. Exp. Biol. 214, 921-927
34. Vlahos, R., Stambas, J., Bozinovski, S., Broughton, B. R., Drummond, G. R., Selemidis, S. (2011) Inhibition of Nox2 oxidase activity ameliorates influenza A virus-induced lung inflammation. PLoS Pathog. 7, e1001271
35. Ye, S., Lowther, S., Stambas, J. (2015) Inhibition of reactive oxygen species production ameliorates inflammation induced by influenza A viruses via upregulation of SOCS1 and SOCS3. J. Virol. 89, 2672-2683
36. Kim, H. J., Kim, C. H., Ryu, J. H., Kim, M. J., Park, C. Y., Lee, J. M., Holtzman, M. J., Yoon, J. H. (2013) Reactive oxygen species induce antiviral innate immune response through IFN-l regulation in human nasal epithelial cells. Am. J. Respir. Cell Mol. Biol. 49, 855-865
37. Lupfer, C., Kanneganti, T. D. (2013) The expanding role of NLRs in antiviral immunity. Immunol. Rev. 255, 13-24
38. Molteni, C. G., Principi, N., Esposito, S. (2014) Reactive oxygen and nitrogen species during viral infections. Free Radic. Res. 48, 1163-1169
39. Strengert, M., Jennings, R., Davanture, S., Hayes, P., Gabriel, G., Knaus, U. G. (2014) Mucosal reactive oxygen species are required for antiviral response: role of Duox in influenza a virus infection. Antioxid. Redox Signal. 20, 2695-2709
40. Venkatesh, B., Lee, A. P., Ravi, V., Maurya, A. K., Lian, M. M., Swann, J. B., Ohta, Y., Flajnik, M. F., Sutoh, Y., Kasahara, M., Hoon, S., Gangu, V., Roy, S. W., Irimia, M., Korzh, V., Kondrychyn, I., Lim, Z. W., Tay, B. H., Tohari, S., Kong, K. W., Ho, S., Lorente-Galdos, B., Quilez, J., Marques- Bonet, T., Raney, B. J., Ingham, P. W., Tay, A., Hillier, L. W., Minx, P., Boehm, T., Wilson, R. K., Brenner, S., Warren, W. C. (2014) Elephant shark genome provides unique insights into gnathostome evolution. Nature 505, 174-179.