Molecular characterisation of porcine miR-155 and its regulatory roles in the TLR3/TLR4 pathways

Developmental and Comparative Immunology

Volumn 39, Issue 1-2, 2013, Pages 110-116

  Li, Congcong ^a   He, Huabin ^a   Zhu, Mengjin ^a   Zhao, Shuhong ^a   Li, Xinyun ^a  

^a Huazhong Agricultural University   (China)

Author keywords

Association; miR 155; Pig; SNP; TLR3; TLR4

Indexed keywords

B7 ANTIGEN; CD86 ANTIGEN; HEMOGLOBIN; MICRORNA 155; POLYINOSINIC POLYCYTIDYLIC ACID; TOLL LIKE RECEPTOR 3; TOLL LIKE RECEPTOR 4; LIPOPOLYSACCHARIDE; MICRORNA;

ADIPOSE TISSUE; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; BASOPHIL; CD3+ T LYMPHOCYTE; CD4+ T LYMPHOCYTE; CD8+ T LYMPHOCYTE; CONTROLLED STUDY; EOSINOPHIL COUNT; ERHUALIAN PIG; ERYTHROCYTE COUNT; GENE FREQUENCY; GENE SEQUENCE; GENETIC TRAIT; GENOTYPE; HEMATOCRIT; HEMATOLOGICAL PARAMETERS; HETEROZYGOSITY; LEUKOCYTE COUNT; LYMPHOCYTE COUNT; MEISHAN PIG; MONOCYTE COUNT; NEUTROPHIL COUNT; NONHUMAN; PIG; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN CLEAVAGE; PROTEIN FUNCTION; PROTEIN LOCALIZATION; QUANTITATIVE ANALYSIS; RNA ISOLATION; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; SPLEEN; TISSUE DISTRIBUTION; UPREGULATION; ANIMAL; CELL LINE; CELLULAR IMMUNITY; CHEMICAL STRUCTURE; GENE EXPRESSION REGULATION; GENETICS; IMMUNOLOGY; LIVESTOCK; METABOLISM; SWINE; TRANSGENE;

ADIPOSE TISSUE; ANIMALS; CELL LINE; GENE EXPRESSION REGULATION; IMMUNITY, CELLULAR; LIPOPOLYSACCHARIDES; LIVESTOCK; MICRORNAS; MOLECULAR STRUCTURE; POLY I-C; POLYMORPHISM, SINGLE NUCLEOTIDE; SIGNAL TRANSDUCTION; SPLEEN; SWINE; TOLL-LIKE RECEPTOR 3; TOLL-LIKE RECEPTOR 4; TRANSGENES;

EID: 84857006029     PISSN: 0145305X     EISSN: 18790089     Source Type: Journal    
DOI: 10.1016/j.dci.2012.01.001     Document Type: Article

References (53)

1. Alexopoulou, L., Holt, A.C., Medzhitov, R., Flavell, R.A., Recognition of double-stranded RNA and activation of NF-kappaB by Toll-like receptor 3. Nature 413 (2001), 732–738.
2. Anglicheau, Dany, Sharma, Vijay K., Ding, Ruchuang, Hummel, Aurélie, Snopkowski, Catherine, Dadhania, Darshana, Seshan, Surya V., Suthanthiran, Manikkam, MicroRNA expression profiles predictive of human renal allograft status. PNAS 106 (2009), 5330–5335.
3. Baggiolini, Marco, Chemokines and leukocyte traffic. Nature 392 (1998), 565–568.
4. Baggiolini, Marco, Dahinden, Clemens A., CC chemokines in allergic inflammation. Immunol. Today 15 (1994), 127–133.
5. Baltimore, D., Boldin, M.P., O'Connell, Ryan M., Rao, Dinesh S., Taganov, Konstantin D., MicroRNAs: new regulators of immune cell development and function. Nat. Immunol. 9 (2008), 839–845.
6. Bartel, David P., MicroRNAs: genomics, biogenesis, mechanism, and function. Cell 116 (2004), 281–297.
7. Barton, Gregory M., Medzhitov, Ruslan, Toll-like receptor signalling pathways. Science 300 (2003), 1524–1525.
8. Bhattacharyya, S., Balakathiresan, N.S., Dalgard, C., Gutti, U., Armistead, D., Jozwik, C., Srivastava, M., Pollard, H.B., Biswas, R., Elevated miR-155 promotes inflammation in cystic fibrosis by driving hyperexpression of interleukin-8. J. Biol. Chem. 286 (2011), 11604–11615.
9. Chen, C., Ridzon, D.A., Broomer, A.J., Zhou, Z., Lee, D.H., Nguyen, Julie T., Barbisin, Maura, Xu, Nan Lan, Mahuvakar, Vikram R., Andersen, Mark R., Lao, Kai Qin, Livak, Kenneth J., Guegler, Karl J., Real-time quantification of microRNAs by stem-loop RT-PCR. Nucleic Acids Res., 33, 2005, 179.
10. Duvigneau, J.C., Hartl, R.T., Groiss, S., Gemeiner, M., Quantitative simultaneous multiplex real-time PCR for the detection of porcine cytokines. J. Immunol. Methods 306 (2005), 16–27.
11. Faraoni, Isabella, Antonetti, Francesca Romana, Cardone, John, Bonmassar, Enzo, miR-155 Gene: a typical multifunctional microRNA. Biochim. Biophys. Acta 1792 (2009), 497–505.
12. Fletcher, Anne L., Lukacs-Kornek, Veronika, Reynoso, Erika D., Pinner, Sophie E., Bellemare-Pelletier, Angelique, Curry, Mark S., Collier, Ai-Ris, Boyd, Richard L., Turley, Shannon J., Lymph node fibroblastic reticular cells directly present peripheral tissue antigen under steady-state and inflammatory conditions. J. Exp. Med. 207 (2010), 689–697.
13. Gatto, G., Rossi, A., Rossi, D., Kroening, S., Bonatti, S., Mallardo, M., Epstein–Barr virus latent membrane protein 1 trans-activates miR-155 transcription through the NF-kappaB pathway. Nucleic Acids Res. 36 (2008), 6608–6619.
14. Haasch, Deanna, Chen, Yung-Wu, Reilly, Regina M., Grace Chiou, X., Koterski, Sandra, Smith, Morey L., Kroeger, Paul, McWeeny, Kerri, Halbert, Donald N., Mollison, Karl W., Djuric, Stevan W., Trevillyan, James M., T cell activation induces a noncoding RNA transcript sensitive to inhibition by immunosuppressant drugs and encoded by the proto-oncogene, BIC. Cell. Immunol. 217 (2002), 78–86.
15. Hardiman, G., Rock, F.L., Balasubramanian, S., Kastelein, R.A., Bazan, J.F., Molecular characterization and modular analysis of human MyD88. Oncogene 13 (1996), 2467–2475.
16. Hoshino, K., Takeuchi, O., Kawai, T., Sanjo, H., Ogawa, T., Takeda, Y., Takeda, K., Akira, S., Toll-like receptor 4 (TLR4)-deficient mice are hyporesponsive to lipopolysaccharide: evidence for TLR4 as the Lps gene product. J. Immunol. 162 (1999), 3749–3752.
17. Imaizumi, T., Tanaka, H., Tajima, A., Yokono, Y., Matsumiya, T., Yoshida, H., Tsuruga, K., Aizawa-Yashiro, T., Hayakari, R., Inoue, I., Ito, E., Satoh, K., IFN-γ and TNF-α synergistically induce microRNA-155 which regulates TAB2/IP-10 expression in human mesangial cells. Am. J. Nephrol. 32 (2010), 462–468.
18. Iorio, Marilena V., Ferracin, Manuela, Liu, Chang-Gong, Veronese, Angelo, Spizzo, Riccardo, Sabbioni, Silvia, Magri, Eros, Pedriali, Massimo, Fabbri, Muller, Campiglio, Manuela, Ménard, Sylvie, Palazzo, Juan P., Rosenberg, Anne, Musiani, Piero, Volinia, Stefano, Nenci, Italo, Calin, George A., Querzoli, Patrizia, Negrini, Massimo, Croce, Carlo M., MicroRNA gene expression deregulation in human breast cancer. Cancer Res. 65 (2005), 7065–7070.
19. Jiang, S., Zhang, H.W., Lu, M.H., He, X.H., Li, Y., Gu, H., Liu, M.F., Wang, E.D., MicroRNA-155 functions as an OncomiR in breast cancer by targeting the suppressor of cytokine signalling 1 gene. Cancer Res. 70 (2010), 3119–3127.
20. Kaisho, Tsuneyasu, Takeuchi, Osamu, Kawai, Taro, Hoshino, Katsuaki, Akira, Shizuo, Endotoxin-induced maturation of MyD88-dificient dendritic cells. J. Immunol. 166 (2001), 5688–5694.
21. Kluiver, Joost, Poppema, Sibrand, de Jong, Debora, Blokzijl, Tjasso, Harms, Geert, Jacobs, Susan, Kroesen, Bart-Jan, van den Berg, Anke, BIC and miR-155 are highly expressed in Hodgkin, primary mediastinal and diffuse large B cell lymphomas. J. Pathol. 207 (2005), 243–249.
22. Lee, Yuriy, Gusev, Jinmai, Jiang, Gerard J., Nuovo, Megan R., Lerner, Wendy L., Frankel, Daniel L., Morgan, Russell G., Postier, Daniel J., Brackett, Thomas D., Schmittgen, Expression profiling identifies microRNA signature in pancreatic cancer. Int. J. Cancer 120 (2007), 1046–1054.
23. Liu, S., Yang, Y., Wu, J., TNFα-induced up-regulation of miR-155 inhibits adipogenesis by down-regulating early adipogenic transcription factors. Biochem. Biophys. Res. Commun. 414 (2011), 618–624.
24. Lodish, H.F., Zhou, B., Liu, G., Chen, C.Z., Micromanagement of the immune system by microRNAs. Nat. Rev. Immunol. 8 (2008), 120–130.
25. Mantovani, Alberto, The chemokine system: redundancy for robust outputs. Immunol. Today 20 (1999), 254–257.
26. Margolick, Joseph B., Carey, Vincent, Muñoz, Alvaro, Frank Polk, B., Giorgi, Janis V., Bauer, Kenneth D., Kaslow, Richard, Rinaldo, Charles, Development of antibodies to HIV-1 is associated with an increase in circulating CD3+ CD4− CD8− lymphocytes. Clin. Immunol. Immunopathol. 51 (1989), 348–361.
27. McCoy, C.E., Sheedy, F.J., Qualls, J.E., Doyle, S.L., Quinn, S.R., Murray, P.J., O'Neill, L.A., IL-10 inhibits miR-155 induction by toll-like receptors. J. Biol. Chem. 285 (2010), 20492–20498.
28. Medzhitov, Ruslan., Janeway, Charles A. Jr., Innate immunity: impact on the adaptive immune response. Curr. Opin. Immunol. 9 (1997), 4–9.
29. Medzhitov, Ruslan, Preston-Hurlburt, Paula, Janeway, Charles. Jr., A human homologue of the drosophila toll protein signals activation of adaptive immunity. Nature 388 (1997), 394–397.
30. Neurath, M.F., Pettersson, S., Meyer Zum Buschenfelde, K.W., Strober, W., Local administration of antisense phosphorothioate oligonucleotides to the p65 subunit of NF- kappaB abrogates established experimental colitis in mice. Nat. Med. 2 (1996), 998–1004.
31. O'Connell, R.M., Taganov, K.D., Boldin, M.P., Cheng, G., Baltimore, D., MicroRNA-155 is induced during the macrophage inflammatory response. Proc. Natl. Acad. Sci. 104 (2007), 1604–1609.
32. O'Connell, Ryan M., Rao, Dinesh S., Chaudhuri, Aadel A., Boldin, Mark P., Taganov, Konstantin D., Nicoll, John, Paquette, Ronald L., Baltimore, David, Sustained expression of microRNA-155 in hematopoietic stem cells causes a myeloproliferative disorder. J. Exp. Med. 205 (2008), 585–594.
33. O'Connell, R.M., Chaudhuri, A.A., Rao, D.S., Baltimore, D., Inositol phosphatase SHIP1 is a primary target of miR-155. Proc. Natl. Acad. Sci. USA 106 (2009), 7113–7118.
34. O'Connell, R.M., Rao, D.S., Chaudhuri, A.A., Baltimore, D., Physiological and pathological roles for microRNAs in the immune system. Nat. Rev. Immunol. 10 (2010), 111–122.
35. Palladino, M.A., Johnson, T.A., Gupta, R., Chapman, J.L., Ojha, P., Members of the Toll-like receptor family of innate immunity pattern-recognition receptors are abundant in the male rat reproductive tract. Biol. Reprod. 76 (2007), 958–964.
36. Pedersen, Irene M., Otero, Dennis, Kao, Elaine, Miletic, Ana V., Hother, Christoffer, Ralfkiaer, Elisabeth, Rickert, Robert C., Gronbaek, Kirsten, David, Michael, Onco-miR-155 targets SHIP1 to promote TNFα-dependent growth of B cell lymphomas. EMBO Mol. Med. 1 (2009), 288–295.
37. Poltorak, A., He, X., Smirnova, I., Liu, M.Y., Van Huffel, C., Du, X., Birdwell, D., Alejos, E., Silva, M., Galanos, C., Freudenberg, M., Ricciardi-Castagnoli, P., Layton, B., Beutler, B., Defective LPS signalling in C3H/HeJ and C57BL/10ScCr mice:mutations in Tlr4 gene. Science 282 (1998), 2085–2088.
38. Ramkissoon, Shakti H., Mainwaring, Lori A., Ogasawara, Yoji, Keyvanfar, Keyvan, Philip McCoy, J. Jr., Sloand, Elaine M., Kajigaya, Sachiko, Hematopoietic-specific microRNA expression in human cells. Leuk. Res. 30 (2006), 643–647.
39. Rodriguez, Antony, Vigorito, Elena, Clare, Simon, Warren, Madhuri V., Couttet, Philippe, Soond, Dalya R., van Dongen, Stijn, Grocock, Russell J., Das, Partha P., Miska, Eric A., Vetrie, David, Okkenhaug, Klaus, Enright, Anton J., Dougan, Gordon, Turner, Martin, Bradley, Allan, Requirement of BIC/microRNA-155 for normal immune function. Science 316 (2007), 608–611.
40. Schletter, Jens, Heine, Holger, Ulmer, Artur J., Rietschel, Ernst T., Molecular mechanisms of endotoxin activity. Arch. Microbiol. 164 (1995), 383–389.
41. Stanczyk, Joanna, Leslie Pedrioli, Deena M., Brentano, Fabia, Sanchez-Pernaute, Olga, Kolling, Christoph, Gay, Renate E., Detmar, Michael, Gay, Steffen, Kyburz, Diego, Altered expression of microRNA in synovial fibroblasts and synovial tissue in rheumatoid arthritis. Arthritis Rheum. 58 (2008), 1001–1009.
42. Tam, W., Ben-Yehuda, D., Hayward, W.S., Bic, a novel gene activated by proviral insertions in avian leukosis virus-induced lymphomas, is likely to function through its noncoding RNA. Mol. Cell. Biol. 17 (1997), 1490–1502.
43. Tan, Z.Q., Liu, F.X., Tang, H.L., Su, Q., Expression and its clinical significance of hsa-miR-155 in serum of endometrial cancer. Zhonghua Fu Chan Ke Za Zhi 45 (2009), 772–774.
44. Tang, B., Xiao, B., Liu, Z., Li, N., Zhu, E.D., Li, B.S., Xie, Q.H., Zhuang, Y., Zou, Q.M., Mao, X.H., Identification of MyD88 as a novel target of miR-155, involved in negative regulation of helicobacter pylori-induced inflammation. FEBS Lett. 584 (2010), 1481–1486.
45. Tatsumi, Y., kumanogoh, A., Saitoh, M., Mizushima, Y., Kimura, K., Suzuki, S., Yagi, H., Horiuchi, A., Ogata, M., Hamaoka, T., Differentiation of thymocytes from CD3−CD4−CD8− through CD3−CD4−CD8′ into more mature stages induced by a thymic stromal cell clone. Proc. Natl. Acad. Sci. USA, Immunology 87 (1990), 2750–2754.
46. Tili, E., Michaille, J.J., Cimino, A., Fabbri, Hannes, Alder, Chang Gong, Liu, George, Adrian, Stefan, Costinean, Calin, Dan Dumitru, Brett, Adair, Muller, Calin, Carlo Maria, Croce, Modulation of miR-155 and miR-125b levels following Lipopolysaccharide/TNF-alpha stimulation and their possible roles in regulating the response to endotoxin shock. J. Immunol. 179 (2007), 5982–5989.
47. Tili, E., Croce, C.M., Michaille, J.J., MiR-155: on the crosstalk between inflammation and cancer. Int. Rev. Immunol. 28 (2009), 264–284.
48. Vargova, K., Curik, N., Burda, P., Basova, P., Kulvait, V., Pospisil, V., Savvulidi, F., Kokavec, J., Necas, E., Berkova, A., Obrtlikova, P., Karban, J., Mraz, M., Pospisilova, S., Mayer, J., Trneny, M., Zavadil, J., Stopka, T., MYB transcriptionally regulates the miR-155 host gene in chronic lymphocytic leukemia. Blood 117 (2011), 3816–3825.
49. Wesch, D., Beetz, S., Kabelitz, D., TLR3 ligand induces a direct costimulatory effect on phosphoantigen stimulated human gdT cells, but not on aminobisphosphonate-stimulated human gdT cells. Haematol. Rep. 2 (2006), 4–5.
50. Yamamoto, Masahiro, Sato, Shintaro, Hemmi, Hiroaki, Hoshino, Katsuaki, Kaisho, Tsuneyasu, Sanjo, Hideki, Takeuchi, Osamu, Sugiyama, Masanaka, Okabe, Masaru, Takeda, Kiyoshi, Akira, Shizuo, Role of adaptor TRIF in the MyD88-independent toll-like receptor signalling pathway. Science 301 (2003), 640–643.
51. Yanaihara, Nozomu, Caplen, Natasha, Bowman, Elise, Seike, Masahiro, Kumamoto, Kensuke, Yi, Ming, Stephens, Robert M., Okamoto, Aikou, Yokota, Jun, Tanaka, Tadao, Calin, George Adrian, Liu, Chang-Gong, Croce, Carlo M., Harris, Curtis C., Unique microRNA molecular profiles in lung cancer diagnosis and prognosis. Cancer Cell 9 (2006), 189–198.
52. Yin, Q., Wang, X., McBride, J., Fewell, C., Flemington, E., B-cell receptor activation induces BIC/miR-155 expression through a conserved AP-1 element. J. Biol. Chem. 283 (2008), 2654–2662.
53. Zhu, J., Hu, X.Q., Guo, G.L., Zhang, Y., Wang, O.C., You, J., Huang, Q.D., Zhang, X.H., Expression and its clinical significance of miR-155 in human primary breast cancer. Zhonghua Wai Ke Za Zhi 48 (2010), 205–208.