Effects of RNA interference-mediated knock-down of hypoxia-inducible factor-α on respiratory burst activity of the Pacific oyster Crassostrea gigas hemocytes

Fish and Shellfish Immunology

Volumn 35, Issue 2, 2013, Pages 476-479

  Choi, Seung Hyuk ^a   Jee, Bo Young ^b   Lee, Su Jin ^a   Cho, Mi Young ^b   Lee, Soon Jeong ^b   Kim, Jin Woo ^b   Jeong, Hyun Do ^a   Kim, Ki Hong ^a  

^a Pukyong National University   (South Korea)

^b National Fisheries Research and Development Institute (NFRDI)   (South Korea)

Author keywords

Crassostrea gigas; Hypoxia inducible factor ; Knock down of HIF ; Respiratory burst activity; RNA interference

Indexed keywords

CRASSOSTREA GIGAS; MAMMALIA; OSTREIDAE;

EID: 84880036118     PISSN: 10504648     EISSN: 10959947     Source Type: Journal    
DOI: 10.1016/j.fsi.2013.05.001     Document Type: Article

References (50)

1. 2 tension. Proc Natl Acad Sci USA 1995, 92:5510-5514.
2. Semenza G.L. Life with oxygen. Science 2007, 318:62-64.
3. 2 sensing: only skin deep?. Cell 2008, 133:206-208.
4. Ohh M., Park C.W., Ivan M., Hoffman M.A., Kim T.Y., Huang L.E., et al. Ubiquitination of hypoxia-inducible factor requires direct binding to the β-domain of the von Hippel-Lindau protein. Nat Cell Biol 2000, 2:423-427.
5. Kallio P.J., Pongratz I., Gradin K., McGuire J., Poellinger L. Activation of hypoxia-inducible factor 1α: posttranscriptional regulation and conformational change by recruitment of the Arnt transcription factor. Proc Natl Acad Sci USA 1997, 94:5667-5672.
6. Poellinger L., Johnson R.S. HIF-1 and hypoxic response: the plot thickens. Curr Opin Genet Dev 2004, 14:81-85.
7. Peyssonnaux C., Datta V., Cramer T., Doedens A., Theodorakis E.A., Gallo R.L., et al. HIF-1α expression regulates the bactericidal capacity of phagocytes. JClin Invest 2005, 115:1806-1815.
8. Sitkovsky M., Lukashev D. Regulation of immune cells by local-tissue oxygen tension: HIF1 α and adenosine receptors. Nat Rev Immunol 2005, 5:712-721.
9. Zinkernagel A.S., Johnson R.S., Nizet V. Hypoxia inducible factor (HIF) function in innate immunity and infection. JMol Med 2007, 85:1339-1346.
10. David E., Tanguy A., Pichavant K., Moraga D. Response of the Pacific oyster Crassostrea gigas to hypoxia exposure under experimental conditions. FEBS J 2005, 272:5635-5652.
11. Le Moullac G., Bacca H., Huvet A., Moal J., Pouvreau S., Van Wormhoudt A. Transcriptional regulation of pyruvate kinase and phosphoenolpyruvate carboxykinase in the adductor muscle of the oyster Crassostrea gigas during prolonged hypoxia. JExp Zool 2007, 307A:371-382.
12. Piontkivska H., Chung J.S., Ivanina A.V., Sokolov E.P., Techa S., Sokolova I.M. Molecular characterization and mRNA expression of two key enzymes of hypoxia-sensing pathways in eastern oysters Crassostrea virginica (Gmelin): hypoxia-inducible factor α (HIF-α) and HIF-prolyl hydroxylase (PHD). Comp Biochem Physiol Part D 2011, 6:103-114.
13. Kawabe S., Yokoyama Y. Role of hypoxia-inducible factor α in response to hypoxia and heat shock in the Pacific oyster Crassostrea gigas. Mar Biotechnol 2012, 14:106-119.
14. Boyd J.N., Burnett L.E. Reactive oxygen intermediate production by oyster hemocytes exposed to hypoxia. JExp Biol 1999, 202:3135-3143.
15. Lambert C., Soudant P., Choquet G., Paillard C. Measurement of Crassostrea gigas hemocyte oxidative metabolism by flow cytometry and the inhibiting capacity of pathogenic vibrios. Fish Shellfish Immunol 2003, 15:225-240.
16. Goedken M., De Guise S. Flow cytometry as a tool to quantify oyster defence mechanisms. Fish Shellfish Immunol 2004, 16:539-552.
17. Scott A.L., Klesius P.H. Chemiluminescence: a novel analysis of phagocytosis in fish. Dev Biol Stand 1981, 49:243-254.
18. Fire A., Xu S., Montgomery M.K., Kostas S.A., Driver S.E., Mello C.C. Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans. Nature 1998, 391:806-811.
19. Fire A. RNA-triggered gene silencing. Trends Genet 1999, 15:358-363.
20. Bernstein E., Denli A.M., Hannon G.J. The rest is silence. RNA 2001, 7:1509-1521.
21. Caplen N.J., Parrish S., Imani F., Fire A., Morgan R.A. Specific inhibition of gene expression by small double-stranded RNA in invertebrate and vertebrate systems. Proc Natl Acad Sci USA 2001, 98:9742-9747.
22. Elbashir S.M., Harborth J., Lendeckel W., Yalcin A., Weber K., Tuschl T. Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells. Nature 2001, 411:494-498.
23. Sharp P.A. RNA Interference - 2001. Genes Dev 2001, 15:485-490.
24. Zamore P.D. RNA interference: listening to the sound of silence. Nat Struct Biol 2001, 8:746-750.
25. Hannon G.J. RNA interference. Nature 2002, 418:244-251.
26. Timmons L., Fire A. Specific interference by ingested dsRNA. Nature 1998, 395:854.
27. Sen G.C. Viruses and interferons. Annu Rev Microbiol 2001, 55:255-281.
28. Hammond S.M., Bernstein E., Beach D., Hannon G.J. An RNA-directed nuclease mediates post-transcriptional gene silencing in Drosophila cells. Nature 2000, 404:293-295.
29. Sharp P.A., Zamore P.D. RNA interference. Science 2000, 287:2431-2433.
30. Suzuki M., Saruwatari K., Kogure T., Yamamoto Y., Nishimura T., Kato T., et al. An acidic matrix protein, Pif, is a key macromolecule for nacre formation. Science 2009, 325:1388-1390.
31. Fang D., Xu G., Hu Y., Pan C., Xie L., Zhang R. Identification of genes directly involved in shell formation and their functions in pearl oyster, Pinctada fucata. PLoS One 2011, 6:e21860.
32. Jiao Y., Wang H., Du X., Zhao X., Wang Q., Huang R., et al. Dermatopontin, a shell matrix protein gene from pearl oyster Pinctada martensii, participates in nacre formation. Biochem Biophys Res Commun 2012, 425:679-683.
33. Fabioux C., Corporeau C., Quillien V., Favrel P., Huvet A. Invivo RNA interference in oyster - vasa silencing inhibits germ cell development. FEBS J 2009, 276:2566-2573.
34. Huvet A., Fleury E., Corporeau C., Quillien V., Daniel J.Y., Riviere G., et al. Invivo RNA interference of a gonad-specific transforming growth factor-β in the Pacific oyster Crassostrea gigas. Mar Biotechnol 2011, 14:402-410.
35. Wang M., Yang J., Zhou Z., Oiu L., Wang L., Zhang H., et al. Aprimitive Toll-like receptor signaling pathway in mollusk Zhikong scallop Chlamys farreri. Dev Comp Immunol 2011, 35:511-520.
36. Takeda K., Kaisho T., Akira S. Toll-like receptors. Annu Rev Immunol 2003, 21:335-376.
37. Akira S., Takeda K. Toll-like receptor signalling. Nat Rev Immunol 2004, 4:499-511.
38. Beutler B. Inferences, questions and possibilities in Toll-like receptor signalling. Nature 2004, 430:257-263.
39. Alexopoulou L., Holt A.C., Medzhitov R., Flavell R.A. Recognition of double-stranded RNA and activation of NF-κB by Toll-like receptor 3. Nature 2001, 413:732-738.
40. Janeway C.A., Medzhitov R. Innate immune recognition. Annu Rev Immunol 2002, 20:197-216.
41. Pallavicini A., Costa M.M., Gestal C., Dreos R., Figueras A., Venier P., et al. High sequence variability of myticin transcripts in hemocytes of immune-stimulated mussels suggests ancient host-pathogen interactions. Dev Comp Immunol 2008, 32:213-216.
42. Green T.J., Barnes A.C. Inhibitor of REL/NF-κB is regulated in Sydney rock oysters in response to specific double-stranded RNA and Vibrio alginolyticus, but the major immune anti-oxidants EcSOD and Prx6 are non-inducible. Fish Shellfish Immunol 2009, 27:260-265.
43. Luo M., Ye S., Xu T., Wu X., Yang P. Molecular characterization of a novel tetraspanin from the oyster, Crassostrea ariakensis: variation, localization and relationship to oyster host defense. Fish Shellfish Immunol 2012, 33:294-304.
44. Wu S.Z., Huang X.D., Li Q., He M.X. Interleukin-17 in pearl oyster (Pinctada fucata): molecular cloning and functional characterization. Fish Shellfish Immunol 2013, 34:1050-1056.
45. Walmsley S.R., Print C., Farahi N., Peyssonnaux C., Johnson R.S., Cramer T., et al. Hypoxia-induced neutrophil survival is mediated by HIF-1α-dependent NF-κB activity. JExp Med 2005, 201:105-115.
46. Peyssonnaux C., Cejudo-Martin P., Doedens A., Zinkernagel A.S., Johnson R.S., Nizet V. Cutting edge: essential role of hypoxia inducible factor-1alpha in development of lipopolysaccharide-induced sepsis. JImmunol 2007, 178:7516-7519.
47. Rius J., Guma M., Schachtrup C., Akassoglou K., Zinkernagel A.S., Nizet V., et al. NF-κB links innate immunity to the hypoxic response through transcriptional regulation of HIF-1alpha. Nature 2008, 453:807-811.
48. Hartmann H., Eltzschig H.K., Wurz H., Hantke K., Rakin A., Yazdi A.S., et al. Hypoxia-independent activation of HIF-1 by enterobacteriaceae and their siderophores. Gastroenterology 2008, 134:756-767.
49. Diebold I., Petry A., Hess J., Görlach A. The NADPH oxidase subunit NOX4 is a new target gene of the hypoxia-inducible factor-1. Mol Biol Cell 2010, 21:2087-2096.
50. Hervouet E., Cízková A., Demont J., Vojtísková A., Pecina P., Franssen-van Hal N.L., et al. HIF and reactive oxygen species regulate oxidative phosphorylation in cancer. Carcinogenesis 2008, 29:1528-1537.