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载脂蛋白E对EAE星形胶质细胞的影响 被引量:4

Effect of apolipoprotein E on astrocyte cytotoxic edema and reactive astrogliosis in mice with experimental autoimmune encephalomyelitis
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摘要 目的探索载脂蛋白E(apolipoprotein E,apo E)对实验性自身免疫性脑脊髓炎(experimental autoimmune encephalomyelitis,EAE)模型小鼠病灶星形胶质细胞的影响。方法采用MOG35-55诱导apo E基因敲除的C57BL/6小鼠(apo E-/-EAE组)及野生型C57BL/6小鼠(普通EAE组),建立EAE模型。取免疫后35 d的EAE小鼠的大脑及脊髓切片,行HE染色,免疫组织化学染色法观察各组小鼠水通道蛋白4(AQP4)和胶质纤维酸性蛋白(GFAP)的表达。结果 apo E-/-EAE组和普通EAE组大脑和脊髓AQP4、GFAP的表达量均高于正常对照组,差异均有统计学意义(P<0.05);apo E-/-EAE组大脑和脊髓AQP4、GFAP表达量均高于普通EAE组,差异均有统计学意义(P<0.05)。结论 EAE中存在星形胶质细胞水肿、增生,apo E缺乏可以加重这一病变。 Objective Abstract: Objective To explore the effect of apolipoprotein E on astrocyte cytotoxic edema and reactive astrogliosis in mice with experimental autoimmune encephalomyelitis. Methods 20 female C57 BL /6 mice were randomly divided into 2 groups. And the third group incuded 10 female apo E- /- mice on a C57 BL /6 background. EAE model was induced by immunized with myelin oligodendrocyte glycoprotein peptides( MOG35-55) in mice. The expression of AQP4 and GFAP was detected by immunohistochemistry. Results The expression of AQP4 and GFAP in the apo E- /- EAE group and common EAE group was more than the control group in brain( P 〈0. 05) and spinal cord( P 〈0. 05).More importantly,the expression of AQP4 and GFAP in the apo E- /- EAE group was beyond the common EAE group in brain( P 〈0. 05) and spinal cord( P 〈0. 05). Conclusion Apo E deficience may aggravate astrocyte cytotoxic edema and increase the formation of reactive astrogliosis in EAE.
出处 《中风与神经疾病杂志》 CAS 北大核心 2015年第1期33-36,共4页 Journal of Apoplexy and Nervous Diseases
基金 国家自然基金项目(项目批准号:81260188 81460194) 广西自然科学基金资助项目(2012GXNSFAA053082) 广西高等学校立项科研项目(201204LX050)
关键词 载脂蛋白E 实验性自身免疫性脑脊髓炎 水通道蛋白4 胶质纤维酸性蛋白 Apolipoprotein E Experimental autoimmune encephalomyelitis Aquaporins 4 Glial fibrillary ac-dic protein
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参考文献11

  • 1韦俊杰,郑明华,梁培霄,陶敏,唐玉兰.载脂蛋白E拟肽对EAE小鼠的髓鞘和轴突损伤的影响[J].中风与神经疾病杂志,2012,29(10):872-875. 被引量:7
  • 2Wei J, Zheng M, Liang P, et al. Apolipoprotein E and its mimetic peptide suppress Thl and Thl7 responses in experimental autoim- mune encephalomyelitis[ J]. Neurobiol Dis,2013,56:59 - 65.
  • 3郑明华,唐玉兰,韦俊杰,梁培霄,陶敏,韦云飞.载脂蛋白E拟肽对实验性自身免疫性脑脊髓炎小鼠脑脊髓CD4^+、CD8^+ T淋巴细胞表达的影响[J].临床神经病学杂志,2013,26(3):198-201. 被引量:8
  • 4Zhang HL,Wu J, Zhu J. The immune-modulatory role of apolipopro- tein E with emphasis on multiple sclerosis and experimental autoim- mune encephalomyelitis [ J ]. Clin Dev Immunol, 2010, 2010: 186813.
  • 5Chiasserini D, Di Filippo M, Candeliere A, et al. CSF proteome anal- ysis in multiple sclerosis patients by two-dimensional electrophoresis [J]. EurJNeuro,2008,15 (9) :998-1001.
  • 6Miyamoto K, Nagaosa N, Motoyama M, et al. Upregulation of water channel aquaporin-4 in experimental autoimmune encephalomyeritis [J]. J Neurol Sci,2009,276 (1 -2) :103 -107.
  • 7Li L,Zhang H, Varrin-Doyer M, et al. Proinflammatory role of aqua- porin-4 in autoimmune neuroinflammation [ J ]. FASEB J, 2011,25 (5) :1556 - 1566.
  • 8Zheng M,Wei J,Tang Y,et al. ApoE-Deficient promotes blood-brain barrier disruption in experimental autoimmune encephalomyelitis via alteration of MMP-9[J]. J Mol Neurusei,2014,54(2) :282 -290.
  • 9Voskuhl RR, Peterson RS, Song B, et al. Reactive astroeytes form scar-like perivascular barriers to leukocytes during adaptive immuneinflammation of the CNS[J]. J Neurosci,2009,29 (37) :11511 - 11522.
  • 10Lavrnja I, Savic D, Bjelobaba I,et al. The effect of ribavirin on reac- tive astrogliosis in experimental autoimmune encephalomyelitis [ J ].J Pharmacol Sci,2012,119 (3) :221 -232.

二级参考文献24

  • 1Karussis D, Michaelson DM, Grigoriadis N, et al. Lack of apolipopro- tein-E exacerbates experimental allergic encephalomyelitis [ J ]. Muh Scler,2003,9 ( 5 ) :476 - 480.
  • 2Laskowitz DT, Fillit H, Yeung N, et al. Apolipoprotein E-derived pep- tides reduce CNS inflammation: implications for therapy of neur01ogi- cal disease [ J ]. Acta Neurol Scand Suppl, 2006,114 ( suppl 185 ) : 15 -20.
  • 3Weaver A, Goncalves Da Silva A, Nuttall RK, et al. An elevated matrix metalloproteinase (MMP) in an animal model of multiple sclerosis is protective by affecting Thl/Th2 polarization [ J]. FASEB J,2005,19 (12) :1668 - 1670.
  • 4Li FQ, Sempowski GD, McKenna SE, et al. Apolipoprotein E-derivedpeptides ameliorate clinical disability and inflammatory infiltrates into the spinal corot in a murine model of multiple sclerosis[ J]. J Pharma- col Ep Ther,2006,318 ( 3 ) :956 - 965.
  • 5Gold R, Linington C, Lassmann H. Understanding pathogenesis and therapy of multiple sclerosis via animal models : 70 years of merits and culprits in experimental autoimmune encephalomyelitis research [ J ]. Brain,2006,129(8) :1953 - 1971.
  • 6Teunissen CE, Dijkstra C, Polman C. Biological markers in CSF and blood for axonal degeneration in multiple sclerosis[ J ]. Lancet Neurol, 2005,4(1) :32 -41.
  • 7Croy JE,Brandon T,Komives EA. Two apolipoprotein E mimetic pep- tides,ApoE(130-149) and ApoE( 141-155)2,bind to LRP1 [J]. Bio- chemistry., 2004,43 ( 23 ) :7328 - 7335.
  • 8Gauhier A,Wu X,Le Moan N,et al. Low-density lipoprotein reeeptor- related protein 1 is an essential receptor for myelin phagoeytosis [ J ]. J Cell Sei,2009,122(8) :1155 -1162.
  • 9Hayashi H, Campenot RB, Vance DE, et al. Apolipoprotein E-contai- ning lipoproteins protect neurons from apoptosis via a signaling path- way involving low-density lipoprotein receptor-related protein-1 [ J ]. J Neurosci ,2007,27(8) : 1933 - 1941.
  • 10Lynch JR,Tang W,Wang H,et al. APOE genotype and an ApoE-mi- metic peptide modify the systemic and central nervous system inflam- matory response [ J ]. J Biol chem,2003,278 (49) : 48529 - 48533.

共引文献10

同被引文献44

  • 1戴华浩,李明昌,石忠松,吴浩强,黄正松,潘伟生.载脂蛋白E基因型与动脉瘤性蛛网膜下腔出血的相关性研究[J].中华神经医学杂志,2006,5(5):465-467. 被引量:9
  • 2Rafiei M, Zarif YM, Sheikholeslami S, et al. Apolipoprotein E polymorphisms status in Iranian patients with multiple sclerosis [J]. J Neurol Sci, 2012, 320(1-2): 22-25. DOI: 10.1016/j.jns.2012.05. 050.
  • 3Erta M, Quintana A, Hidalgo J. Interleukin-6, a major cytokine in the central nervous system[J]. Int J Biol Sci, 2012, 8(9): 1254-1266. DOI: 10.7150/ijbs.4679.
  • 4Vojdani A, Lambert J. The role of Thl7 in neuroimmune disorders: target for CAM therapy. Part I [J]. Evid Based Complement Altemat Med, 2011, 2011: 927294. DOI: 10.1093/ ecam/nep062.
  • 5Jadidi-Niaragh F, Mirshaficy A. Thl7 cell, the new player of neuroinflammatory process in multiple sclerosis [J]. Scand J Immunol, 2011, 74(1): 1-13. DOI: 10.1111/j.1365-3083.2011.02536.
  • 6Bonora M, De Marchi E, Patergnani S, et al. Tumor necrosis factor-α impairs oligodendroglial differentiation through a process[J]. Cell Death Differ, 2014, 21(8) 1198-1208. DOI: 10.1038/cdd.2014.35.
  • 7Iwanoto S, Iwai S, Tsujiyama K, et al. TNF-α drives human CD14+ monocytes to differentiate into CD70+ dendritic cells evokingThl andTh17 resonses [J]. J Immunol, 2007, 179 (3): 1449-1457.
  • 8Wei J, Zheng M, Liang P, et al. Apolipoprotein E and its mimetic peptide suppress Thl and Thl7 responses in experimental autoimmune encephalomyelitis[J]. Neurobiol Dis, 2013, 56: 59-65. DOI: 10.1016/j.nbd.2013.04.009.
  • 9Almolda B, Costa M, Montoya M, et al. Increase in Th17 and T-reg lymphocytes and decrease of IL22 correlate with the recovery phase of acute EAE in rat[J]. PLoS One, 2011, 6(11): e27473. DOI: 10.1371/joumal.pone.0027473.
  • 10Li FQ, Sempowski GD, MeKenna SE, et al. Apolipoprotein E-derived peptides ameliorate clinical disability and inflammatory infiltrates into the spinal cord in a murine model of multiple sclerosis[J]. J Pharmacol Exp Ther, 2006, 318(3): 956-965. DOI: 10.1124/jpet. 106.103671.

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