Suppression of the Toll-like receptors 3 mediated pro-inflammatory gene expressions by progenitor cell differentiation and proliferation factor in chicken DF-1 cells |
Hwang, Eunmi
(Division of Cosmetics and Biotechnology, College of Life and Health Sciences, Hoseo University)
Kim, Hyungkuen (Division of Cosmetics and Biotechnology, College of Life and Health Sciences, Hoseo University) Truong, Anh Duc (Department of Agricultural Convergence Technology, Jeonbuk National University) Kim, Sung-Jo (Division of Cosmetics and Biotechnology, College of Life and Health Sciences, Hoseo University) Song, Ki-Duk (Department of Agricultural Convergence Technology, Jeonbuk National University) |
1 | Nailwal H, Chan FKM. Necroptosis in anti-viral inflammation. Cell Death Differ. 2019;26:4-13. https://doi.org/10.1038/s41418-018-0172-x DOI |
2 | Anwar MA, Basith S, Choi S. Negative regulatory approaches to the attenuation of Toll-like receptor signaling. Exp Mol Med. 2013;45:e11. https://doi.org/10.1038/emm.2013.28 DOI |
3 | Kurochkina N, Guha U. SH3 domains: modules of protein-protein interactions. Biophys Rev. 2013;5:29-39. https://doi.org/10.1007/s12551-012-0081-z DOI |
4 | Deshmukh V, O'Green AL, Bossard C, Seo T, Lamangan L, Ibanez M, et al. Modulation of the Wnt pathway through inhibition of CLK2 and DYRK1A by lorecivivint as a novel, potentially disease-modifying approach for knee osteoarthritis treatment. Osteoarthr Cartil. 2019;27:1347-60. https://doi.org/10.1016/j.joca.2019.05.006 DOI |
5 | Petsalaki E, Zachos G. Clks 1, 2 and 4 prevent chromatin breakage by regulating the Aurora B-dependent abscission checkpoint. Nat Commun. 2016;7:11451. https://doi.org/10.1038/ncomms11451 DOI |
6 | Chauhan JS, Mishra NK, Raghava GPS. Identification of ATP binding residues of a protein from its primary sequence. BMC Bioinformatics. 2009;10:434. https://doi.org/10.1186/1471-2105-10-434 DOI |
7 | Peroval MY, Boyd AC, Young JR, Smith AL. A critical role for MAPK signalling pathways in the transcriptional regulation of toll like receptors. PLOS ONE. 2013;8:e51243. https://doi.org/10.1371/journal.pone.0051243 DOI |
8 | Matsumoto M, Funami K, Tanabe M, Oshiumi H, Shingai M, Seto Y, et al. Subcellular localization of Toll-like receptor 3 in human dendritic cells. J Immunol. 2003;171:3154-62. https://doi.org/10.4049/jimmunol.171.6.3154 DOI |
9 | Tian W, Zhao C, Hu Q, Sun J, Peng X. Roles of Toll-like receptors 2 and 6 in the inflammatory response to Mycoplasma gallisepticum infection in DF-1 cells and in chicken embryos. Dev Comp Immunol. 2016;59:39-47. https://doi.org/10.1016/j.dci.2016.01.008 DOI |
10 | Foster D. Development of a spontaneously immortalized chicken embryo fibroblastic cell line. Virology. 1998;248:305-11. DOI |
11 | Surai PF, Kochish II, Kidd MT. Redox homeostasis in poultry: regulatory roles of NF-κB. Antioxidants. 2021;10:186. https://doi.org/10.3390/antiox10020186 DOI |
12 | McGuffin LJ, Adiyaman R, Maghrabi AHA, Shuid AN, Brackenridge DA, Nealon JO, et al. IntFOLD: an integrated web resource for high performance protein structure and function prediction. Nucleic Acids Res. 2019;47:W408-13. https://doi.org/10.1093/nar/gkz322 DOI |
13 | Guo ZY, Li JL, Zhang L, Jiang Y, Gao F, Zhou GH. Effects of alpha-lipoic acid supplementation in different stages on growth performance, antioxidant capacity and meat quality in broiler chickens. Br Poult Sci. 2014;55:635-43. https://doi.org/10.1080/00071668.2014.958057 DOI |
14 | Breunig M, Hohwieler M, Seufferlein T, Glockner J, Liebau S, Kleger A. PPDPF impacts pancreatic progenitor cell formation derived from human pluripotent stem cell. Z Gastroenterol. 2018;56:e234. https://doi.org/10.1055/s-0038-1668739 DOI |
15 | Ma N, Wang YK, Xu S, Ni QZ, Zheng QW, Zhu B, et al. PPDPF alleviates hepatic steatosis through inhibition of mTOR signaling. Nat Commun. 2021;12:3059. https://doi.org/10.1038/s41467-021-23285-8 DOI |
16 | Matsumoto M, Oshiumi H, Seya T. Antiviral responses induced by the TLR3 pathway. Rev Med Virol. 2011;21:67-77. https://doi.org/10.1002/rmv.680 DOI |
17 | Chovatiya R, Medzhitov R. Stress, inflammation, and defense of homeostasis. Mol Cell. 2014;54:281-8. https://doi.org/10.1016/j.molcel.2014.03.030 DOI |
18 | Bsibsi M, Ravid R, Gveric D, van Noort JM. Broad expression of Toll-like receptors in the human central nervous system. J Neuropathol Exp Neurol. 2002;61:1013-21. https://doi.org/10.1093/jnen/61.11.1013 DOI |
19 | Yao C, Oh JH, Lee DH, Bae JS, Jin CL, Park CH, et al. Toll-like receptor family members in skin fibroblasts are functional and have a higher expression compared to skin keratinocytes. Int J Mol Med. 2015;35:1443-50. https://doi.org/10.3892/ijmm.2015.2146 DOI |
20 | Kariko K, Buckstein M, Ni H, Weissman D. Suppression of RNA recognition by Toll-like receptors: the impact of nucleoside modification and the evolutionary origin of RNA. Immunity. 2005;23:165-75. https://doi.org/10.1016/j.immuni.2005.06.008 DOI |
21 | Mora Izaguirre MO, Quester K, Petranovski V, Gonzalez Davalos L, Pina Garza E, Shimada Miyasaka A, et al. Effect of nanostructured zeolite with lipoic acid on performance and carcass yield in broiler. Rev Mex Cienc Pecu. 2018;9:185-202. https://doi.org/10.22319/rmcp.v9i2.4315 DOI |
22 | Keestra AM, van Putten JPM. Unique properties of the chicken TLR4/MD-2 complex: selective lipopolysaccharide activation of the MyD88-dependent pathway. J Immunol. 2008;181:4354-62. https://doi.org/10.4049/jimmunol.181.6.4354 DOI |
23 | Xiao Y, Lai Y, Yu Y, Jiang P, Li Y, Wang C, et al. The exocrine differentiation and proliferation factor (EXDPF) gene promotes ovarian cancer tumorigenesis by up-regulating DNA replication pathway. Front Oncol. 2021;11:669603. https://doi.org/10.3389/fonc.2021.669603 DOI |
24 | Stowell NC, Seideman J, Raymond HA, Smalley KA, Lamb RJ, Egenolf DD, et al. Long-term activation of TLR3 by poly (I:C) induces inflammation and impairs lung function in mice. Respir Res. 2009;10:43. https://doi.org/10.1186/1465-9921-10-43 DOI |
25 | Leung YHC, Nicholls JM, Ho CK, Sia SF, Mok CKP, Valkenburg SA, et al. Highly pathogenic avian influenza A H5N1 and pandemic H1N1 virus infections have different phenotypes in Toll-like receptor 3 knockout mice. J Gen Virol. 2014;95:1870-9. https://doi.org/10.1099/vir.0.066258-0 DOI |
26 | Blom N, Gammeltoft S, Brunak S. Sequence and structure-based prediction of eukaryotic protein phosphorylation sites. J Mol Biol. 1999;294:1351-62. https://doi.org/10.1006/jmbi.1999.3310 DOI |
27 | Walsh I, Di Domenico T, Tosatto SCE. RUBI: rapid proteomic-scale prediction of lysine ubiquitination and factors influencing predictor performance. Amino Acids. 2014;46:853-62. https://doi.org/10.1007/s00726-013-1645-3 DOI |
28 | McGuffin LJ, Shuid AN, Kempster R, Maghrabi AHA, Nealon JO, Salehe BR, et al. Accurate template-based modeling in CASP12 using the IntFOLD4-TS, ModFOLD6, and ReFOLD methods. Proteins. 2018;86:335-44. https://doi.org/10.1002/prot.25360 DOI |
29 | Beug H, von Kirchbach A, Doderlein G, Conscience JF, Graf T. Chicken hematopoietic cells transformed by seven strains of defective avian leukemia viruses display three distinct phenotypes of differentiation. Cell. 1979;18:375-90. https://doi.org/10.1016/0092-8674(79)90057-6 DOI |
30 | Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods. 2001;25:402-8. https://doi.org/10.1006/meth.2001.1262 DOI |
31 | Vittrant B, Leclercq M, Martin-Magniette ML, Collins C, Bergeron A, Fradet Y, et al. Identification of a transcriptomic prognostic signature by machine learning using a combination of small cohorts of prostate cancer. Front Genet. 2020;11:550894. https://doi.org/10.3389/fgene.2020.550894 DOI |
32 | Akira S, Takeda K. Toll-like receptor signalling. Nat Rev Immunol. 2004;4:499-511. https://doi.org/10.1038/nri1391 DOI |
33 | Jiang Z, Song J, Qi F, Xiao A, An X, Liu N, et al. Exdpf is a key regulator of exocrine pancreas development controlled by retinoic acid and ptf1a in zebrafish. PLOS Biol. 2008;6:e293. https://doi.org/10.1371/journal.pbio.0060293 DOI |
34 | Funami K, Matsumoto M, Oshiumi H, Akazawa T, Yamamoto A, Seya T. The cytoplasmic 'linker region' in Toll-like receptor 3 controls receptor localization and signaling. Int Immunol. 2004;16:1143-54. https://doi.org/10.1093/intimm/dxh115 DOI |
35 | Karpala AJ, Lowenthal JW, Bean AG. Activation of the TLR3 pathway regulates IFNβ production in chickens. Dev Comp Immunol. 2008;32:435-44. https://doi.org/10.1016/j.dci.2007.08.004 DOI |
36 | Cheng J, Sun Y, Zhang X, Zhang F, Zhang S, Yu S, et al. Toll-like receptor 3 inhibits Newcastle disease virus replication through activation of pro-inflammatory cytokines and the type-1 interferon pathway. Arch Virol. 2014;159:2937-48. https://doi.org/10.1007/s00705-014-2148-6 DOI |
37 | Wang Q, Miller DJ, Bowman ER, Nagarkar DR, Schneider D, Zhao Y, et al. MDA5 and TLR3 initiate pro-inflammatory signaling pathways leading to rhinovirus-induced airways inflammation and hyperresponsiveness. PLOS Pathog. 2011;7:e1002070. https://doi.org/10.1371/journal.ppat.1002070 DOI |
38 | Jiang Z, Schatzmayr G, Mohnl M, Applegate TJ. Net effect of an acute phase response-partial alleviation with probiotic supplementation. Poult Sci. 2010;89:28-33. https://doi.org/10.3382/ps.2009-00464 DOI |
39 | Wong R, Balachandran A, Mao AYQ, Dobson W, Gray-Owen S, Cochrane A. Differential effect of CLK SR kinases on HIV-1 gene expression: potential novel targets for therapy. Retrovirology. 2011;8:47. https://doi.org/10.1186/1742-4690-8-47 DOI |
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