Temporal and Spatial Dynamics of Astroglial Reaction and Immune Response in Cuprizone-Induced Demyelination.


Journal

Neurotoxicity research
ISSN: 1476-3524
Titre abrégé: Neurotox Res
Pays: United States
ID NLM: 100929017

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 19 06 2019
accepted: 25 10 2019
revised: 03 10 2019
pubmed: 14 11 2019
medline: 15 12 2020
entrez: 14 11 2019
Statut: ppublish

Résumé

The cuprizone (CPZ)-induced demyelination is a relatively reproducible animal model and has been extremely useful for identifying the specific cellular and molecular signals that regulate oligodendrocyte survival and efficiency of oligodendrogenesis and remyelination. Here, we reported the temporal and spatial dynamics of astroglial reaction and immune response in CPZ-induced demyelinating model. CPZ did not induce significant microglia and astrocyte reaction after 2 weeks of feeding. After 4-6 weeks of CPZ feeding, microglia and astrocytes were markedly migrated and accumulated in myelin sheath. Simultaneously, the expression of tight junction protein ZO-1 was declined and the infiltration of CD4+IFNγ+ and CD4+IL-17+ T cells was increased in the brain, accompanied by increased production of IFN-γ and IL-17 in the extract of brain. However, the levels of IFN-γ and IL-17 were reduced, while IL-6 and TNF-α were elevated in the supernatant of splenocytes. At the 4th and 6th weeks of feeding, CPZ caused astrocyte activation and upregulated the expression of BDNF, CNTF, and IGF-II, providing a neurotrophic microenvironment in the brain. At this stage, NG2+ and PDGF-Rα+ oligodendroglia progenitor cells were enhanced in the corpus callosum, but the myelin sheath is still severely lost. Therefore, targeting microglia to improve the inflammatory microenvironment should contribute to the remyelination.

Identifiants

pubmed: 31721051
doi: 10.1007/s12640-019-00129-4
pii: 10.1007/s12640-019-00129-4
doi:

Substances chimiques

Cuprizone 5N16U7E0AO

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

587-601

Subventions

Organisme : National Natural Science Foundation of China
ID : 81473577
Organisme : National Natural Science Foundation of China
ID : 81371414
Organisme : Shanxi Scholarship Council of China
ID : 2014-7

Références

An Y, Chen Q, Quan N (2011) Interleukin-1 exerts distinct actions on different cell types of the brain in vitro. J Inflamm Res 2011:11–20. https://doi.org/10.2147/JIR.S15357
doi: 10.2147/JIR.S15357 pubmed: 22022205
Arnett HA, Mason J, Marino M, Suzuki K, Matsushima GK, ing JP (2001) TNF alpha promotes proliferation of oligodendrocyte progenitors and remyelination. Nat Neurosci 4(11):1116–1122. https://doi.org/10.1038/nn738
doi: 10.1038/nn738 pubmed: 11600888
Barres, Burne, Holtmann et al (1996) Ciliary neurotrophic factor enhances the rate of oligodendrocyte generation. Mol Cell Neurosci 8:146–156. https://doi.org/10.1006/mcne.1996.0053
doi: 10.1006/mcne.1996.0053 pubmed: 8954629
Bartus K, Burnside ER, Galino J, James ND, Bennett DLH, Bradbury EJ (2019) ErbB receptor signaling directly controls oligodendrocyte progenitor cell transformation and spontaneous remyelination after spinal cord injury. Glia 67:1036–1046. https://doi.org/10.1002/glia.23586
doi: 10.1002/glia.23586 pubmed: 30637799 pmcid: 6491970
Behan PO, Chaudhuri A (2014) EAE is not a useful model for demyelinating disease. Mult Scler Relat Disord 3:565–574. https://doi.org/10.1016/j.msard.2014.06.003
doi: 10.1016/j.msard.2014.06.003 pubmed: 26265268
Behrangi N, Namvar N, Ataei M, Dizaji S, Javdani G, Sanati MH (2017) MMP9 gene expression variation by ingesting tart cherry and p-coumaric acid during remyelination in the cuprizone mouse model. Acta Med Iran 55(9):539–549
pubmed: 29202545
Brambilla R (2019) The contribution of astrocytes to the neuroinflammatory response in multiple sclerosis and experimental autoimmune encephalomyelitis. Acta Neuropathol 137:757–783. https://doi.org/10.1007/s00401-019-01980-7
doi: 10.1007/s00401-019-01980-7 pubmed: 30847559 pmcid: 6483860
Calabretta S, Vogel G, Yu Z et al (2018) Loss of PRMT5 promotes PDGFRalpha degradation during oligodendrocyte differentiation and myelination. Dev Cell 46:426-440.e5. https://doi.org/10.1016/j.devcel.2018.06.025
doi: 10.1016/j.devcel.2018.06.025 pubmed: 30057274
Fletcher JL, Wood RJ, Nguyen J, Norman EML, Jun CMK, Prawdiuk AR, Biemond M, Nguyen HTH, Northfield SE, Hughes RA, Gonsalvez DG, Xiao J, Murray SS (2018) Targeting TrkB with a brain-derived neurotrophic factor mimetic promotes myelin repair in the brain. J Neurosci 38:7088–7099. https://doi.org/10.1523/JNEUROSCI.0487-18.2018
doi: 10.1523/JNEUROSCI.0487-18.2018 pubmed: 29976621 pmcid: 6596092
Franklin RJM, Ffrench-Constant C, Edgar JM, Smith KJ (2012) Neuroprotection and repair in multiple sclerosis. Nat Rev Neurol 8:624–634. https://doi.org/10.1038/nrneurol.2012.200
doi: 10.1038/nrneurol.2012.200 pubmed: 23026979
Freeman L, Guo H, David CN, Brickey WJ, Jha S, Ting JP (2017) NLR members NLRC4 and NLRP3 mediate sterile inflammasome activation in microglia and astrocytes. J Exp Med 214:1351–1370. https://doi.org/10.1084/jem.20150237
doi: 10.1084/jem.20150237 pubmed: 28404595 pmcid: 5413320
Govier-Cole AE, Wood RJ, Fletcher JL et al (2019) Inhibiting bone morphogenetic protein 4 type i receptor signaling promotes remyelination by potentiating oligodendrocyte differentiation. eNeuro 6:e0399–e0318. https://doi.org/10.1523/ENEURO.0399-18.2019
doi: 10.1523/ENEURO.0399-18.2019
Gudi V, Gingele S, Skripuletz T, Stangel M (2014) Glial response during cuprizone-induced de- and remyelination in the CNS: lessons learned. Front Cell Neurosci 8:73. https://doi.org/10.3389/fncel.2014.00073
doi: 10.3389/fncel.2014.00073 pubmed: 24659953 pmcid: 3952085
Herder V, Hansmann F, Stangel M, Schaudien D, Rohn K, Baumgärtner W, Beineke A (2012) Cuprizone inhibits demyelinating leukomyelitis by reducing immune responses without virus exacerbation in an infectious model of multiple sclerosis. J Neuroimmunol 244(1-2):84–93. https://doi.org/10.1016/j.jneuroim.2012.01.010
doi: 10.1016/j.jneuroim.2012.01.010 pubmed: 22329906
Herranz E, Gianni C, Louapre C et al (2016) Neuroinflammatory component of gray matter pathology in multiple sclerosis. Ann Neurol 80:776–790. https://doi.org/10.1002/ana.24791
doi: 10.1002/ana.24791 pubmed: 27686563 pmcid: 5115951
Kang Z, Liu L, Spangler R et al (2012) IL-17-induced Act1-mediated signaling is critical for cuprizone-induced demyelination. J Neurosci 13;32(24):8284–8292. https://doi.org/10.1523/JNEUROSCI.0841-12.2012
doi: 10.1523/JNEUROSCI.0841-12.2012
Kim M, Carman CV, Springer TA (2003) Bidirectional transmembrane signaling by cytoplasmic domain separation in integrins. Science 301:1720–1725. https://doi.org/10.1126/science.1084174
doi: 10.1126/science.1084174 pubmed: 14500982
Kipp M, Clarner T, Dang J, Copray S, Beyer C (2009) The cuprizone animal model: new insights into an old story. Acta Neuropathol 118(6):723–736. https://doi.org/10.1007/s00401-009-0591-3
doi: 10.1007/s00401-009-0591-3 pubmed: 19763593
Kipp M, Nyamoya S, Hochstrasser T, Amor S (2017) Multiple sclerosis animal models: a clinical and histopathological perspective. Brain Pathol 27:123–137. https://doi.org/10.1111/bpa.12454
doi: 10.1111/bpa.12454 pubmed: 27792289 pmcid: 8029141
Klegeris A, Giasson BI, Zhang H et al (2006) Alpha-synuclein and its disease-causing mutants induce ICAM-1 and IL-6 in human astrocytes and astrocytoma cells. FASEB J 20:2000–2008. https://doi.org/10.1096/fj.06-6183com
doi: 10.1096/fj.06-6183com pubmed: 17012252
Komegae EN, Souza TA, Grund LZ, Lima C, Lopes-Ferreira M (2017) Multiple functional therapeutic effects of TnP: A small stable synthetic peptide derived from fish venom in a mouse model of multiple sclerosis. PLoS One 12(2):e0171796. https://doi.org/10.1371/journal.pone.0171796 eCollection 2017
doi: 10.1371/journal.pone.0171796 pubmed: 28235052 pmcid: 5325231
Komoly S, Hudson LD, Webster HD, Bondy CA (1992) Insulin-like growth factor I gene expression is induced in astrocytes during experimental demyelination. Proc Natl Acad Sci U S A 89:1894–1898. https://doi.org/10.1073/pnas.89.5.1894
doi: 10.1073/pnas.89.5.1894 pubmed: 1371885 pmcid: 48560
Kramann N, Menken L, Pfortner R et al (2019) Glial fibrillary acidic protein expression alters astrocytic chemokine release and protects mice from cuprizone-induced demyelination. Glia 67:1308–1319. https://doi.org/10.1002/glia.23605
doi: 10.1002/glia.23605 pubmed: 30801815
Labunets IF, Rodnichenko AE (2019) Melatonin effects in young and aged mice with toxic cuprizone-induced model of demyelination. Adv Gerontol 32(3):338–346
pubmed: 31512419
Lassmann H, Bradl M (2017) Multiple sclerosis: experimental models and reality. Acta Neuropathol 133:223–244. https://doi.org/10.1007/s00401-016-1631-4
doi: 10.1007/s00401-016-1631-4 pubmed: 27766432
Li W, Suwanwela NC, Patumraj S (2017) Curcumin prevents reperfusion injury following ischemic stroke in rats via inhibition of NFkappaB, ICAM-1, MMP-9 and caspase-3 expression. Mol Med Rep 16:4710–4720. https://doi.org/10.3892/mmr.2017.7205
doi: 10.3892/mmr.2017.7205 pubmed: 28849007 pmcid: 5647023
Lub M, van Kooyk Y, van Vliet SJ, Figdor CG (1997) Dual role of the actin cytoskeleton in regulating cell adhesion mediated by the integrin lymphocyte function-associated molecule-1. Mol Biol Cell 8:341–351. https://doi.org/10.1091/mbc.8.2.341
doi: 10.1091/mbc.8.2.341 pubmed: 9190212 pmcid: 276084
Lutton EM, Razmpour R, Andrews AM, Cannella LA, Son YJ, Shuvaev VV, Muzykantov VR, Ramirez SH (2017) Acute administration of catalase targeted to ICAM-1 attenuates neuropathology in experimental traumatic brain injury. Sci Rep 7:3846. https://doi.org/10.1038/s41598-017-03309-4
doi: 10.1038/s41598-017-03309-4 pubmed: 28630485 pmcid: 5476649
Madadi S, Pasbakhsh P, Tahmasebi F, Mortezaee K, Khanehzad M, Boroujeni FB, Noorzehi G, Kashani IR (2019) Astrocyte ablation induced by La-aminoadipate (L-AAA) potentiates remyelination in a cuprizone demyelinating mouse model. Metab Brain Dis 34:593–603. https://doi.org/10.1007/s11011-019-0385-9
doi: 10.1007/s11011-019-0385-9 pubmed: 30652255
Mahad DH, Trapp BD, Lassmann H (2015) Pathological mechanisms in progressive multiple sclerosis. Lancet Neurol 14:183–193. https://doi.org/10.1016/S1474-4422(14)70256-X
doi: 10.1016/S1474-4422(14)70256-X pubmed: 25772897
Mana P, Fordham SA, Staykova MA et al (2009) Demyelination caused by the copper chelator cuprizone halts T cell mediated autoimmune neuroinflammation. J Neuroimmunol 210:13–21. https://doi.org/10.1016/j.jneuroim.2009.02.013
doi: 10.1016/j.jneuroim.2009.02.013 pubmed: 19344958
McMahon EJ, Suzuki K, Matsushima GK et al (2002) Peripheral macrophage recruitment in cuprizone-induced CNS demyelination despite an intact blood-brain barrier. J Neuroimmunol 130(1-2):32–45. https://doi.org/10.1016/s0165-5728(02)00205-9
doi: 10.1016/s0165-5728(02)00205-9 pubmed: 12225886
Miklossy J, Doudet DD, Schwab C et al (2006) Role of ICAM-1 in persisting inflammation in Parkinson disease and MPTP monkeys. Exp Neurol 197:275–283. https://doi.org/10.1016/j.expneurol.2005.10.034
doi: 10.1016/j.expneurol.2005.10.034 pubmed: 16336966
Nakahara H, Konishi Y, Beach TG, Yamada N, Makino S, Tooyama I (2010) Infiltration of T lymphocytes and expression of icam-1 in the hippocampus of patients with hippocampal sclerosis. Acta Histochem Cytochem 43:157–162. https://doi.org/10.1267/ahc.10022
doi: 10.1267/ahc.10022 pubmed: 21245982 pmcid: 3015053
Nystad AE, Wergeland S, Aksnes L, Myhr KM, Bø L, Torkildsen O (2014) Effect of high-dose 1.25 dihydroxyvitamin D3 on remyelination in the cuprizone model. APMIS 122(12):1178–1186. https://doi.org/10.1111/apm.12281
doi: 10.1111/apm.12281 pubmed: 24862867
Patel R, Hossain MA, German N, Al-Ahmad AJ (2018) Gliotoxin penetrates and impairs the integrity of the human blood-brain barrier in vitro. Mycotoxin Res 34:257–268. https://doi.org/10.1007/s12550-018-0320-7
doi: 10.1007/s12550-018-0320-7 pubmed: 30006720
Petkovic F, Campbell IL, Gonzalez B, Castellano B (2017) Reduced cuprizone-induced cerebellar demyelination in mice with astrocyte-targeted production of IL-6 is associated with chronically activated, but less responsive microglia. J Neuroimmunol 310:97–102. https://doi.org/10.1016/j.jneuroim.2017.07.003
doi: 10.1016/j.jneuroim.2017.07.003 pubmed: 28778453
Pfeifenbring S, Bunyan RF, Metz I, Röver C, Huppke P, Gärtner J, Lucchinetti CF, Brück W (2015) Extensive acute axonal damage in pediatric multiple sclerosis lesions. Ann Neurol 77:655–667. https://doi.org/10.1002/ana.24364
doi: 10.1002/ana.24364 pubmed: 25612167 pmcid: 4523885
Pirko I, Johnson AJ (2008) Neuroimaging of demyelination and remyelination models. Curr Top Microbiol Immunol 318:241–266
pubmed: 18219821
Praet J, Guglielmetti C, Berneman Z, van der Linden A, Ponsaerts P (2014) Cellular and molecular neuropathology of the cuprizone mouse model: clinical relevance for multiple sclerosis. Neurosci Biobehav Rev 47:485–505. https://doi.org/10.1016/j.neubiorev.2014.10.004
doi: 10.1016/j.neubiorev.2014.10.004 pubmed: 25445182
Remington LT, Babcock AA, Zehntner SP, Owens T (2007) Microglial recruitment, activation, and proliferation in response to primary demyelination. Am J Pathol 170(5):1713–1724. https://doi.org/10.2353/ajpath.2007.060783
doi: 10.2353/ajpath.2007.060783 pubmed: 17456776 pmcid: 1854965
Scott GS, Kean RB, Fabis MJ et al (2004) ICAM-1 upregulation in the spinal cords of PLSJL mice with experimental allergic encephalomyelitis is dependent upon TNF-alpha production triggered by the loss of blood-brain barrier integrity. J Neuroimmunol 155:32–42. https://doi.org/10.1016/j.jneuroim.2004.05.011
doi: 10.1016/j.jneuroim.2004.05.011 pubmed: 15342194
Skripuletz T, Hackstette D, Bauer K et al (2013) Astrocytes regulate myelin clearance through recruitment of microglia during cuprizone-induced demyelination. Brain 136:147–167. https://doi.org/10.1093/brain/aws262
doi: 10.1093/brain/aws262 pubmed: 23266461
Sui R-X, Miao Q, Wang J et al (2019) Protective and therapeutic role of Bilobalide in cuprizone-induced demyelination. Int Immunopharmacol 66:69–81. https://doi.org/10.1016/j.intimp.2018.09.041
doi: 10.1016/j.intimp.2018.09.041 pubmed: 30445309
Vega-Riquer JM, Mendez-Victoriano G, Morales-Luckie RA, Gonzalez-Perez O (2019) Five Decades of Cuprizone, an Updated Model to Replicate Demyelinating Diseases. Curr Neuropharmacol 17:129–141. https://doi.org/10.2174/1570159X15666170717120343
doi: 10.2174/1570159X15666170717120343 pubmed: 28714395 pmcid: 6343207
Weller RO (1998) Pathology of cerebrospinal fluid and interstitial fluid of the CNS: significance for Alzheimer disease, prion disorders and multiple sclerosis. J Neuropathol Exp Neurol 57(10):885–894. https://doi.org/10.1097/00005072-199810000-00001
doi: 10.1097/00005072-199810000-00001 pubmed: 9786239
Wu T, Zhang A, Lu H, Cheng Q (2018) The Role and Mechanism of Borneol to Open the Blood-Brain Barrier. Integr Cancer Ther 17:806–812. https://doi.org/10.1177/1534735418767553
doi: 10.1177/1534735418767553 pubmed: 29652199 pmcid: 6142104
Yang J, Fei M, Gu Y et al (2008) Evaled expression of ICAM-1 and its ligands in the rat spinal cord following lipopolysaccharide intraspinal injection. Neuromolecular Med 10(4):385–392. https://doi.org/10.1007/s12017-008-8049-7
doi: 10.1007/s12017-008-8049-7 pubmed: 18759008
Zhao C, Ma D, Zawadzka M, Fancy SP, Elis-Williams L, Bouvier G, Stockley JH, de Castro GM, Wang B, Jacobs S, Casaccia P, Franklin RJ (2015) Sox2 sustains recruitment of oligodendrocyte progenitor cells following CNS demyelination and primes them for differentiation during remyelination. J Neurosci 35:11482–11499. https://doi.org/10.1523/JNEUROSCI.3655-14.2015
doi: 10.1523/JNEUROSCI.3655-14.2015 pubmed: 26290228 pmcid: 6605237
Zheng P, Fu H, Wei G, Wei Z, Zhang J, Ma X, Rui D, Meng X, Ming L (2016) Antigen-oriented T cell migration contributes to myelin peptide induced-EAE and immune tolerance. Clin Immunol 169:36–46. https://doi.org/10.1016/j.clim.2016.06.004
doi: 10.1016/j.clim.2016.06.004 pubmed: 27327113

Auteurs

Jun An (J)

The Key Research Laboratory of Benefiting Qi for Acting Blood Circulation Method to Treat Multiple Sclerosis of State Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Taiyuan, 030024, China.

Jun-Jun Yin (JJ)

The Key Research Laboratory of Benefiting Qi for Acting Blood Circulation Method to Treat Multiple Sclerosis of State Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Taiyuan, 030024, China.

Yan He (Y)

The Key Research Laboratory of Benefiting Qi for Acting Blood Circulation Method to Treat Multiple Sclerosis of State Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Taiyuan, 030024, China.

Ruo-Xuan Sui (RX)

The Key Research Laboratory of Benefiting Qi for Acting Blood Circulation Method to Treat Multiple Sclerosis of State Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Taiyuan, 030024, China.

Qiang Miao (Q)

The Key Research Laboratory of Benefiting Qi for Acting Blood Circulation Method to Treat Multiple Sclerosis of State Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Taiyuan, 030024, China.

Qing Wang (Q)

The Key Research Laboratory of Benefiting Qi for Acting Blood Circulation Method to Treat Multiple Sclerosis of State Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Taiyuan, 030024, China.

Jie-Zhong Yu (JZ)

Institute of Brain Science, Shanxi Datong University, Datong, 037009, China.

Jing-Wen Yu (JW)

Institute of Brain Science, Shanxi Datong University, Datong, 037009, China.

Fu-Dong Shi (FD)

Department of Neurology, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ, 85013, USA.

Cun-Gen Ma (CG)

The Key Research Laboratory of Benefiting Qi for Acting Blood Circulation Method to Treat Multiple Sclerosis of State Administration of Traditional Chinese Medicine, Shanxi University of Chinese Medicine, Taiyuan, 030024, China. macungen2001@163.com.
Institute of Brain Science, Shanxi Datong University, Datong, 037009, China. macungen2001@163.com.

Bao-Guo Xiao (BG)

Institute of Neurology, Huashan Hospital, Institutes of Brain Science and State Key Laboratory of Medical Neurobiology, Fudan University, Shanghai, 200025, China. bgxiao@shmu.edu.cn.

Articles similaires

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male
Humans Meals Time Factors Female Adult

Classifications MeSH