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Volumn 20, Issue 2, 2000, Pages 660-665

Restricted expression of G86R Cu/Zn superoxide dismutase in astrocytes results in astrocytosis but does not cause motoneuron degeneration

Author keywords

Amyotrophic lateral sclerosis; Glia; Gliosis; Glutamate; Mouse; Transgenic

Indexed keywords

SUPEROXIDE DISMUTASE;

EID: 0034651102     PISSN: 02706474     EISSN: None     Source Type: Journal    
DOI: 10.1523/jneurosci.20-02-00660.2000     Document Type: Article
Times cited : (306)

References (30)
  • 1
    • 0028364108 scopus 로고
    • Demonstration of poly-N-acetyl lactosamine residues in amoeboid and ramified microglial cells in rat brain by tomato lectin binding
    • Acarin L, Vela JM, Gonzalez B, Castellano B (1994) Demonstration of poly-N-acetyl lactosamine residues in amoeboid and ramified microglial cells in rat brain by tomato lectin binding. J Histochem Cytochem 42:1033-1041.
    • (1994) J Histochem Cytochem , vol.42 , pp. 1033-1041
    • Acarin, L.1    Vela, J.M.2    Gonzalez, B.3    Castellano, B.4
  • 2
    • 0032032844 scopus 로고    scopus 로고
    • Aberrant RNA splicing in sporadic amyotrophic lateral sclerosis
    • Bai G, Lipton SA (1998) Aberrant RNA splicing in sporadic amyotrophic lateral sclerosis. Neuron 20:353-366.
    • (1998) Neuron , vol.20 , pp. 353-366
    • Bai, G.1    Lipton, S.A.2
  • 4
    • 0031868461 scopus 로고    scopus 로고
    • Elevated hydroxyl radical generation in vivo in an animal model of amyotrophic lateral sclerosis
    • Bogdanov MB, Ramos L, Xu Z, Beal MF (1998) Elevated hydroxyl radical generation in vivo in an animal model of amyotrophic lateral sclerosis. J Neurochem 71:1321-1324.
    • (1998) J Neurochem , vol.71 , pp. 1321-1324
    • Bogdanov, M.B.1    Ramos, L.2    Xu, Z.3    Beal, M.F.4
  • 5
    • 0028256226 scopus 로고
    • GFAP promoter directs astrocyte- specific expression in transgenic mice
    • Brenner M, Kissebeth WC, Su Y, Besnard F, Messing A (1994) GFAP promoter directs astrocyte- specific expression in transgenic mice. J Neurosci 14:1030-1037.
    • (1994) J Neurosci , vol.14 , pp. 1030-1037
    • Brenner, M.1    Kissebeth, W.C.2    Su, Y.3    Besnard, F.4    Messing, A.5
  • 8
    • 0032579962 scopus 로고    scopus 로고
    • Glutamate uptake is decreased tardively in the spinal cord of FALS mice
    • Canton T, Pratt J, Stutzmann JM, Boireau A (1998) Glutamate uptake is decreased tardively in the spinal cord of FALS mice. NeuroReport 9:775-778.
    • (1998) NeuroReport , vol.9 , pp. 775-778
    • Canton, T.1    Pratt, J.2    Stutzmann, J.M.3    Boireau, A.4
  • 9
    • 0032530566 scopus 로고    scopus 로고
    • Transgenic mice for interleukin 3 develop motor neuron degeneration associated with auto immune reaction against spinal cord motor neurons
    • Chavany C, Vicario-Abejon C, Miller G, Jendobi, M (1998) Transgenic mice for interleukin 3 develop motor neuron degeneration associated with auto immune reaction against spinal cord motor neurons. Proc Natl Acad Sci USA 95:11354-11359.
    • (1998) Proc Natl Acad Sci USA , vol.95 , pp. 11354-11359
    • Chavany, C.1    Vicario-Abejon, C.2    Miller, G.3    Jendobi, M.4
  • 10
    • 0030833449 scopus 로고    scopus 로고
    • Decreased zinc affinity of amyotrophic lateral sclerosis-associated superoxide dismutase mutants leads to enhanced catalysis of tyrosine nitration by peroxynitrite
    • Crow JP, Sampson JB, Zhuang Y, Thompson JA, and Beckman JS (1997) Decreased zinc affinity of amyotrophic lateral sclerosis-associated superoxide dismutase mutants leads to enhanced catalysis of tyrosine nitration by peroxynitrite. J Neurochem 69:1936-1944.
    • (1997) J Neurochem , vol.69 , pp. 1936-1944
    • Crow, J.P.1    Sampson, J.B.2    Zhuang, Y.3    Thompson, J.A.4    Beckman, J.S.5
  • 11
    • 0027946294 scopus 로고
    • Development of central nervous system pathology in a murine transgenic model of ALS
    • Dal Canto MC, Gurney ME (1994) Development of central nervous system pathology in a murine transgenic model of ALS. Am J Pathol 145:1271-1280.
    • (1994) Am J Pathol , vol.145 , pp. 1271-1280
    • Dal Canto, M.C.1    Gurney, M.E.2
  • 16
    • 0032032013 scopus 로고    scopus 로고
    • Aberrant RNA processing in a neurodegenerative disease: The cause for absent EAAT2, a glutamate transporter in amyotrophic lateral sclerosis
    • Lin CLG, Bristol LA, Jin L, Dykes-Hoberg M, Crawford T, Clawson L, and Rothstein JD (1998) Aberrant RNA processing in a neurodegenerative disease: the cause for absent EAAT2, a glutamate transporter in amyotrophic lateral sclerosis. Neuron 20:589-602.
    • (1998) Neuron , vol.20 , pp. 589-602
    • Lin, C.L.G.1    Bristol, L.A.2    Jin, L.3    Dykes-Hoberg, M.4    Crawford, T.5    Clawson, L.6    Rothstein, J.D.7
  • 18
    • 0031768026 scopus 로고    scopus 로고
    • Protein modification by the lipid peroxidation product 4-hydroxynonenal in the spinal cords of amyotrophic lateral sclerosis patients
    • Pedersen WA, Fu W, Keller JN, Markesberry WR, Appel SA, Smith RG, Kasarkis E, Mattson MP (1998) Protein modification by the lipid peroxidation product 4-hydroxynonenal in the spinal cords of amyotrophic lateral sclerosis patients. Ann Neurol 44:819-824.
    • (1998) Ann Neurol , vol.44 , pp. 819-824
    • Pedersen, W.A.1    Fu, W.2    Keller, J.N.3    Markesberry, W.R.4    Appel, S.A.5    Smith, R.G.6    Kasarkis, E.7    Mattson, M.P.8
  • 21
    • 0028888945 scopus 로고
    • Transgenic mice expressing an altered superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis
    • Ripps M E, Huntley GW, Hof PR, Morrison JH, and Gordon JW (1995) Transgenic mice expressing an altered superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis. Proc Natl Acad Sci USA 92:689-693.
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 689-693
    • Ripps, M.E.1    Huntley, G.W.2    Hof, P.R.3    Morrison, J.H.4    Gordon, J.W.5
  • 23
    • 0026597010 scopus 로고
    • Decreased glutamate transport by the brain and spinal cord in amyotrophic lateral sclerosis
    • Rothstein JD, Martin LJ, Kuncl RW (1992) Decreased glutamate transport by the brain and spinal cord in amyotrophic lateral sclerosis. New Engl J Med 326:1464-1468.
    • (1992) New Engl J Med , vol.326 , pp. 1464-1468
    • Rothstein, J.D.1    Martin, L.J.2    Kuncl, R.W.3
  • 25
    • 0029030610 scopus 로고
    • Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis
    • Rothstein JD, Van Kammen M, Levey AI, Martin LJ, Kuncl RW (1995) Selective loss of glial glutamate transporter GLT-1 in amyotrophic lateral sclerosis. Ann Neurol 38:73-84.
    • (1995) Ann Neurol , vol.38 , pp. 73-84
    • Rothstein, J.D.1    Van Kammen, M.2    Levey, A.I.3    Martin, L.J.4    Kuncl, R.W.5
  • 28
    • 0033366461 scopus 로고    scopus 로고
    • SOD1 mutants linked to amyotrophic lateral sclerosis selectively inactivate a glial glutamate transporter
    • Trotti D, Rolfs A, Danbolt NC, Brown Jr RH, Hediger MA (1999) SOD1 mutants linked to amyotrophic lateral sclerosis selectively inactivate a glial glutamate transporter. Nat Neurosci 2:427-433.
    • (1999) Nat Neurosci , vol.2 , pp. 427-433
    • Trotti, D.1    Rolfs, A.2    Danbolt, N.C.3    Brown R.H., Jr.4    Hediger, M.A.5
  • 29
    • 0029966363 scopus 로고    scopus 로고
    • Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions
    • Tu PH, Rau P, Robinson KA, Gurney ME, Trojanowski JQ, and Lee V (1996) Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions. Proc Natl Acad Sci USA 93:3155-3160.
    • (1996) Proc Natl Acad Sci USA , vol.93 , pp. 3155-3160
    • Tu, P.H.1    Rau, P.2    Robinson, K.A.3    Gurney, M.E.4    Trojanowski, J.Q.5    Lee, V.6
  • 30
    • 0029053881 scopus 로고
    • An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria
    • Wong PC, Pardo CA, Borchelt DR, Lee MK, Copeland NG, Jenkins NA, Sisodia SS, Cleveland DW, Price DL (1995) An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria. Neuron 14:1105-1116.
    • (1995) Neuron , vol.14 , pp. 1105-1116
    • Wong, P.C.1    Pardo, C.A.2    Borchelt, D.R.3    Lee, M.K.4    Copeland, N.G.5    Jenkins, N.A.6    Sisodia, S.S.7    Cleveland, D.W.8    Price, D.L.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.