期刊论文详细信息
Particle and Fibre Toxicology
Preliminary expression profile of cytokines in brain tissue of BALB/c mice with Angiostrongylus cantonensis infection
Zhongdao Wu1  Zhiyue Lv1  Yi Zhao2  Xin Zeng1  Siqi Luo1  Lian Xu1  Qi Liao4  Jie Wei1  Xiaoying Wu1  Liping Yu3 
[1] Key Laboratory for Tropical Diseases Control, The Ministry of Education, Sun Yat-sen University, Guangzhou, China;Advanced Computing Research Laboratory, Institute of Computing Technology, Chinese Academy of Sciences, Beijing, China;Department of Parasitology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China;Department of Preventive Medicine, School of Medicine, Ningbo University, Ningbo, China
关键词: Chemokine;    Cytokine;    Mouse model;    Eosinophil;    Angiostrongylus cantonensis;   
Others  :  1224193
DOI  :  10.1186/s13071-015-0939-6
 received in 2015-01-22, accepted in 2015-06-05,  发布年份 2015
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【 摘 要 】

Background

Angiostrongylus cantonensis (A. cantonensis) infection can result in increased risk of eosinophilic meningitis. Accumulation of eosinophils and inflammation can result in the A. cantonensis infection playing an important role in brain tissue injury during this pathological process. However, underlying mechanisms regarding the transcriptomic responses during brain tissue injury caused by A. cantonensis infection are yet to be elucidated. This study is aimed at identifying some genomic and transcriptomic factors influencing the accumulation of eosinophils and inflammation in the mouse brain infected with A. cantonensis.

Methods

An infected mouse model was prepared based on our laboratory experimental process, and then the mouse brain RNA Libraries were constructed for deep Sequencing with Illumina Genome Analyzer. The raw data was processed with a bioinformatics’ pipeline including Refseq genes expression analysis using cufflinks, annotation and classification of RNAs, lncRNA prediction as well as analysis of co-expression network. The analysis of Refseq data provides the measure of the presence and prevalence of transcripts from known and previously unknown genes.

Results

This study showed that Cys-Cys (CC) type chemokines such as CCL2, CCL8, CCL1, CCL24, CCL11, CCL7, CCL12 and CCL5 were elevated significantly at the late phase of infection. The up-regulation of CCL2 indicated that the worm of A. cantonensis had migrated into the mouse brain at an early infection phase. CCL2 could be induced in the brain injury during migration and CCL2 might play a major role in the neuropathic pain caused by A. cantonensis infection. The up-regulated expression of IL-4, IL-5, IL-10, and IL-13 showed Th2 cell predominance in immunopathological reactions at late infection phase in response to infection by A. cantonensis. These different cytokines can modulate and inhibit each other and function as a network with the specific potential to drive brain eosinophilic inflammation. The increase of ATF-3 expression at 21 dpi suggested the injury of neuronal cells at late phase of infection. 1217 new potential lncRNA were candidates of interest for further research.

Conclusions

These cytokine networks play an important role in the development of central nervous system inflammation caused by A. cantonensis infection.

【 授权许可】

   
2015 Yu et al.

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【 参考文献 】
  • [1]Moreira VL, Giese EG, Melo FT, Simoes RO, Thiengo SC, Maldonado A et al.. Endemic angiostrongyliasis in the Brazilian Amazon: natural parasitism of Angiostrongylus cantonensis in Rattus rattus and R. norvegicus, and sympatric giant African land snails, Achatina fulica. Acta Trop. 2013; 125(1):90-7.
  • [2]Eamsobhana P. Angiostrongyliasis in Thailand: epidemiology and laboratory investigations. Hawaii J Med Public Health. 2013; 72(6 Suppl 2):28-32.
  • [3]Lunn JA, Lee R, Smaller J, MacKay BM, King T, Hunt GB et al.. Twenty two cases of canine neural angiostronglyosis in eastern Australia (2002–2005) and a review of the literature. Parasit Vectors. 2012; 5:70. BioMed Central Full Text
  • [4]Deng ZH, Lv S, Lin JY, Lin RX, Pei FQ. An outbreak of angiostrongyliasis in Guanging, People’s Republic of China: migrants vulnerable to an emerging disease. Southeast Asian J Trop Med Public Health. 2011; 42(5):1047-53.
  • [5]Evans-Gilbert T, Lindo JF, Henry S, Brown P, Christie CD. Severe eosinophilic meningitis owing to Angiostrongylus cantonensis in young Jamaican children: case report and literature review. Paediatr Int Child Health. 2014; 34(2):148-52.
  • [6]Padilla-Docal B, Iglesias-Gonzalez I, Bu-Coifiu-Fanego R, Socarras-Hernandez CA, Dorta-Contreras AJ. Intrathecal activation as a typical immune response within the central nervous system in angiostrongyliasis. Am J Trop Med Hyg. 2013; 88(2):230-5.
  • [7]Slom T, Johnson S. Eosinophilic Meningitis. Curr Infect Dis Rep. 2003; 5(4):322-8.
  • [8]Wiwanitkit S, Wiwanitkit V. Eosinophilic meningitis due to Angiostrongylus cantonensis with confirmed finding of intrathecal parasite. Arq Neuropsiquiatr. 2014; 72(3):261.
  • [9]Morassutti AL, Thiengo SC, Fernandez M, Sawanyawisuth K, Graeff-Teixeira C. Eosinophilic meningitis caused by Angiostrongylus cantonensis: an emergent disease in Brazil. Mem Inst Oswaldo Cruz. 2014; 109(4):399-407.
  • [10]Liu LH, He HJ, Lv ZY, Wei J, Zeng X, Liang JY et al.. The mRNA level of the galectin-10 of Angiostrongylus cantonensis induced by reactive oxygen stress. Parasitol Res. 2013; 112(3):933-43.
  • [11]Intapan PM, Kittimongkolma S, Niwattayakul K, Sawanyawisuth K, Maleewong W. Cerebrospinal fluid cytokine responses in human eosinophilic meningitis associated with angiostrongyliasis. J Neurol Sci. 2008; 267(1–2):17-21.
  • [12]Lv S, Zhang Y, Chen SR, Wang LB, Fang W, Chen F et al.. Human angiostrongyliasis outbreak in Dali China. PLoS Negl Trop Dis. 2009; 3(9): Article ID e520
  • [13]Oehler E, Ghawche F, Delattre A, Berberian A, Levy M, Valour F. Angiostrongylus cantonensis eosinophilic meningitis: a clinical study of 42 consecutive cases in French Polynesia. Parasitol Int. 2014; 63(3):544-9.
  • [14]Iwata T, Fujii T, Morii K, Saito M, Sugiyama J, Nishio H et al.. Cytokine profile in cervical mucosa of Japanese patients with cervical intraepithelial neoplasia. Int J Clin Oncol. 2014; 20(1):126-33.
  • [15]Teixeira MM, Wells TN, Lukacs NW, Proudfoot AE, Kunkel SL, Williams TJ et al.. Chemokine-induced eosinophil recruitment: Evidence of a role for endogenous eotaxin in an in vivo allergy model in mouse skin. J Clin Invest. 1997; 100(7):1657-66.
  • [16]Lukacs NW, Standiford TJ, Chensue SW, Kunkel RG, Strieter RM, Kunkel SL. C-C chemokine-induced eosinophil chemotaxis during allergic airway inflammation. J Leukoc Biol. 1996; 60(5):573-8.
  • [17]Lukacs NW, Prosser DM, Wiekowski M, Lira SA, Cook DN. Requirement for the chemokine receptor CCR6 in allergic pulmonary inflammation. J Exp Med. 2001; 194(4):551-5.
  • [18]Gerard C, Rollins BJ. Chemokines and disease. Nat Immunol. 2001; 2(2):108-15.
  • [19]Ying S, Robinson DS, Meng Q, Barata LT, McEuen AR, Buckley MG et al.. C-C chemokines in allergen-induced late-phase cutaneous responses in atopic subjects: association of eotaxin with early 6-hour eosinophils, and of eotaxin-2 and monocyte chemoattractant protein-4 with the later 24-hour tissue eosinophilia, and relationship to basophils and other C-C chemokines (monocyte chemoattractant protein-3 and RANTES). J Immunol. 1999; 163(7):3976-84.
  • [20]Chang EE, Chung LY, Yen CM. Kinetics of change in the eotaxin concentration in serum and cerebrospinal fluid of mice infected with Angiostrongylus cantonensis. Parasitol Res. 2004; 92(2):137-41.
  • [21]Li S, Yang F, Ji P, Zeng X, Wu X, Wei J et al.. Eosinophil chemotactic chemokine profilings of the brain from permissive and non-permissive hosts infected with Angiostrongylus cantonenis. Parasitol Res. 2014; 113(2):517-25.
  • [22]Feng Y, Zeng X, Li WH, Wang WC, Ou-Yang LS, Sun X et al.. Animal model of human disease with optic neuritis: neuropapillitis in a rat model infected with Angiostrongylus cantonensis. Parasitol Res. 2014; 113(11):4005-13.
  • [23]Yu L, Liao Q, Zeng X, Lv Z, Zheng H, Zhao Y et al.. MicroRNA expressions associated with eosinophilic meningitis caused by Angiostrongylus cantonensis infection in a mouse model. Eur J Clin Microbiol Infect Dis. 2014; 33(8):1457-65.
  • [24]Bauer BK, Isom SC, Spate LD, Whitworth KM, Spollen WG, Blake SM et al.. Transcriptional profiling by deep sequencing identifies differences in mRNA transcript abundance in in vivo-derived versus in vitro-cultured porcine blastocyst stage embryos. Biol Reprod. 2010; 83(5):791-8.
  • [25]Zhao Y, Luo H, Chen X, Xiao Y, Chen R. Computational methods to predict long noncoding RNA functions based on co-expression network. Methods Mol Biol. 2014; 1182:209-18.
  • [26]Liao Q, Liu C, Yuan X, Kang S, Miao R, Xiao H et al.. Large-scale prediction of long non-coding RNA functions in a coding-non-coding gene co-expression network. Nucleic Acids Res. 2011; 39(9):3864-78.
  • [27]OuYang L, Wei J, Wu Z, Zeng X, Li Y, Jia Y et al.. Differences of larval development and pathological changes in permissive and nonpermissive rodent hosts for Angiostrongylus cantonensis infection. Parasitol Res. 2012; 111(4):1547-57.
  • [28]Van Steenwinckel J, Auvynet C, Sapienza A, Reaux-Le Goazigo A, Combadiere C, Melik PS. Stromal cell-derived CCL2 drives neuropathic pain states through myeloid cell infiltration in injured nerve. Brain Behav Immun. 2015; 45:198-210.
  • [29]Guo YQ, Zheng LN, Wei JF, Hou XL, Yu SZ, Zhang WW et al.. Expression of CCL2 and CCR2 in the hippocampus and the interventional roles of propofol in rat cerebral ischemia/reperfusion. Exp Ther Med. 2014; 8(2):657-61.
  • [30]Yao Y, Tsirka SE. Monocyte chemoattractant protein-1 and the blood–brain barrier. Cell Mol Life Sci. 2014; 71(4):683-97.
  • [31]Peterson KE, Errett JS, Wei T, Dimcheff DE, Ransohoff R, Kuziel WA et al.. MCP-1 and CCR2 contribute to non-lymphocyte-mediated brain disease induced by Fr98 polytropic retrovirus infection in mice: role for astrocytes in retroviral neuropathogenesis. J Virol. 2004; 78(12):6449-58.
  • [32]Tanaka T, Minami M, Nakagawa T, Satoh M. Enhanced production of monocyte chemoattractant protein-1 in the dorsal root ganglia in a rat model of neuropathic pain: possible involvement in the development of neuropathic pain. Neurosci Res. 2004; 48(4):463-9.
  • [33]Graber DJ, Costine BA, Hickey WF. Early inflammatory mediator gene expression in two models of traumatic brain injury: ex vivo cortical slice in mice and in vivo cortical impact in piglets. J Neuroinflammation. 2015; 12(1):76. BioMed Central Full Text
  • [34]Hammond MD, Taylor RA, Mullen MT, Ai Y, Aguila HL, Mack M et al.. CCR2+ Ly6C (hi) inflammatory monocyte recruitment exacerbates acute disability following intracerebral hemorrhage. J Neurosci. 2014; 34(11):3901-9.
  • [35]Bose S, Cho J. Role of chemokine CCL2 and its receptor CCR2 in neurodegenerative diseases. Arch Pharm Res. 2013; 36(9):1039-50.
  • [36]Choi JW, Herr DR, Noguchi K, Yung YC, Lee CW, Mutoh T et al.. LPA receptors: subtypes and biological actions. Annu Rev Pharmacol Toxicol. 2010; 50:157-86.
  • [37]Islam SA, Chang DS, Colvin RA, Byrne MH, McCully ML, Moser B et al.. Mouse CCL8, a CCR8 agonist, promotes atopic dermatitis by recruiting IL-5+ T (H)2 cells. Nat Immunol. 2011; 12(2):167-77.
  • [38]Lee YG, Jeong JJ, Nyenhuis S, Berdyshev E, Chung S, Ranjan R et al.. Recruited alveolar macrophages, in response to airway epithelial-derived MCP-1/CCL2, regulate airway inflammation and remodeling in allergic asthma. Am J Respir Cell Mol Biol. 2014; 52(6):772-84.
  • [39]Suzuki Y, Asano K, Niimi K, Miyata J, Shiraishi Y, Fukunaga K et al.. TP receptor-mediated release of eosinophil chemotactic activity from human bronchial smooth muscle cells. Eur J Pharmacol. 2008; 600(1–3):133-9.
  • [40]de Nadai P, Chenivesse C, Gilet J, Porte H, Vorng H, Chang Y et al.. CCR5 usage by CCL5 induces a selective leukocyte recruitment in human skin xenografts in vivo. J Invest Dermatol. 2006; 126(9):2057-64.
  • [41]Meyer-Hoffert U, Lezcano-Meza D, Bartels J, Montes-Vizuet AR, Schroder JM, Teran LM. Th2- and to a lesser extent Th1-type cytokines upregulate the production of both CXC (IL-8 and gro-alpha) and CC (RANTES, eotaxin, eotaxin-2, MCP-3 and MCP-4) chemokines in human airway epithelial cells. Int Arch Allergy Immunol. 2003; 131(4):264-71.
  • [42]Feng Y, Zeng X, Li WH, Wang WC, Chen W, Ou-Yang LS et al.. The pathogenesis of optic neuritis caused by Angiostrongylus cantonensis in BALB/c mice. Parasit Vectors. 2014; 7:339. BioMed Central Full Text
  • [43]Tsai HC, Lee BY, Yen CM, Wann SR, Lee SS, Chen YS. Dexamethasone inhibits brain apoptosis in mice with eosinophilic meningitis caused by Angiostrongylus cantonensis infection. Parasit Vectors. 2015; 8(1):200. BioMed Central Full Text
  • [44]Garcia G, Taille C, Laveneziana P, Bourdin A, Chanez P, Humbert M. Anti-interleukin-5 therapy in severe asthma. Eur Respir Rev. 2013; 22(129):251-7.
  • [45]Fontes JA, Rose NR, Cihakova D. The varying faces of IL-6: From cardiac protection to cardiac failure. Cytokine. 2015; 74(1):62-8.
  • [46]Kunz S, Wolk K, Witte E, Witte K, Doecke WD, Volk HD et al.. Interleukin (IL)-19, IL-20 and IL-24 are produced by and act on keratinocytes and are distinct from classical ILs. Exp Dermatol. 2006; 15(12):991-1004.
  • [47]Azuma YT, Matsuo Y, Kuwamura M, Yancopoulos GD, Valenzuela DM, Murphy AJ et al.. Interleukin-19 protects mice from innate-mediated colonic inflammation. Inflamm Bowel Dis. 2010; 16(6):1017-28.
  • [48]Hsu YH, Li HH, Sung JM, Chen WT, Hou YC, Chang MS. Interleukin-19 mediates tissue damage in murine ischemic acute kidney injury. PLoS One. 2013; 8(2): Article ID e56028
  • [49]Liao YC, Liang WG, Chen FW, Hsu JH, Yang JJ, Chang MS. IL-19 induces production of IL-6 and TNF-alpha and results in cell apoptosis through TNF-alpha. J Immunol. 2002; 169(8):4288-97.
  • [50]Stenberg L, Kanje M, Dolezal K, Dahlin LB. Expression of activating transcription factor 3 (ATF 3) and caspase 3 in Schwann cells and axonal outgrowth after sciatic nerve repair in diabetic BB rats. Neurosci Lett. 2012; 515(1):34-8.
  • [51]Cai B, Song XQ, Cai JP, Zhang S. HOTAIR: acancer-related long non-coding RNA. Neoplasma. 2014; 61(4):379-91.
  • [52]Leung A, Trac C, Jin W, Lanting L, Akbany A, Saetrom P et al.. Novel long noncoding RNAs are regulated by angiotensin II in vascular smooth muscle cells. Circ Res. 2013; 113(3):266-78.
  • [53]Deng K, Guo X, Wang H, Xia J. The lncRNA-MYC regulatory network in cancer. Tumour Biol. 2014; 35(10):9497-503.
  • [54]Tran VG, Court F, Duputie A, Antoine E, Aptel N, Milligan L et al.. H19 antisense RNA can up-regulate Igf2 transcription by activation of a novel promoter in mouse myoblasts. PLoS One. 2012; 7(5): Article ID e37923
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