Protective effect of neurofilament heavy gene overexpression in motor neuron disease induced by mutant superoxide dismutase

被引:153
作者
Couillard-Després, S [1 ]
Zhu, QZ
Wong, PC
Price, DL
Cleveland, DW
Julien, JP
机构
[1] McGill Univ, Montreal Gen Hosp, Neurosci Res Ctr, Res Inst, Montreal, PQ H3G 1A4, Canada
[2] Johns Hopkins Univ, Sch Med, Neuropathol Lab, Baltimore, MD 21205 USA
[3] Univ Calif San Diego, Dept Med, Ludwig Inst Canc Res, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Neurosci, Ludwig Inst Canc Res, La Jolla, CA 92093 USA
关键词
amyotrophic lateral sclerosis; transgenic mice; intermediate filaments;
D O I
10.1073/pnas.95.16.9626
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To investigate the role of neurofilaments in motor neuron disease caused by superoxide dismutase (SOD1) mutations, transgenic mice expressing a amyotrophic lateral sclerosis-linked SOD1 mutant (SOD1(G37R)) were mated with transgenic mice expressing human neurofilament heavy (NF-H) subunits, Unexpectedly, expression of human NF-H transgenes increased by up to 65%, the mean lifespan of SOD1(G37R) mice. Microscopic examination corroborated the protective effect of NF-H protein against SOD1 toxicity. Although massive neurodegeneration occurred in 1-yr-old mice expressing SOD1(G37R) alone, spinal root axons and motor neurons were remarkably spared in doubly SOD1(G37R);NF-H-transgenic littermates.
引用
收藏
页码:9626 / 9630
页数:5
相关论文
共 43 条
  • [1] ALS, SOD AND PEROXYNITRITE
    BECKMAN, JS
    CARSON, M
    SMITH, CD
    KOPPENOL, WH
    [J]. NATURE, 1993, 364 (6438) : 584 - 584
  • [2] NEUROFILAMENT LIGHT AND POLYADENYLATED MESSENGER-RNA LEVELS ARE DECREASED IN AMYOTROPHIC-LATERAL-SCLEROSIS MOTOR-NEURONS
    BERGERON, C
    BERICMASKAREL, K
    MUNTASSER, S
    WEYER, L
    SOMERVILLE, MJ
    PERCY, ME
    [J]. JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1994, 53 (03) : 221 - 230
  • [3] Elevated free nitrotyrosine levels, but not protein-bound nitrotyrosine or hydroxyl radicals, throughout amyotrophic lateral sclerosis (ALS)-like disease implicate tyrosine nitration as an aberrant in vivo property of one familial ALS-linked superoxide dismutase 1 mutant
    Bruijn, LI
    Beal, MF
    Becher, MW
    Schulz, JB
    Wong, PC
    Price, DL
    Cleveland, DW
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) : 7606 - 7611
  • [4] PROXIMAL AXONAL ENLARGEMENT IN MOTOR NEURON DISEASE
    CARPENTER, S
    [J]. NEUROLOGY, 1968, 18 (09) : 841 - +
  • [5] Mechanisms of selective motor neuron death in transgenic mouse models of motor neuron disease
    Cleveland, DW
    Bruijn, LI
    Wong, PC
    Marszalek, JR
    Vechio, JD
    Lee, MK
    Xu, XS
    Borchelt, DR
    Sisodia, SS
    Price, DL
    [J]. NEUROLOGY, 1996, 47 (04) : S54 - S61
  • [6] DEFECTIVE AXONAL-TRANSPORT IN A TRANSGENIC MOUSE MODEL OF AMYOTROPHIC-LATERAL-SCLEROSIS
    COLLARD, JF
    COTE, F
    JULIEN, JP
    [J]. NATURE, 1995, 375 (6526) : 61 - 64
  • [7] PROGRESSIVE NEURONOPATHY IN TRANSGENIC MICE EXPRESSING THE HUMAN NEUROFILAMENT HEAVY GENE - A MOUSE MODEL OF AMYOTROPHIC-LATERAL-SCLEROSIS
    COTE, F
    COLLARD, JF
    JULIEN, JP
    [J]. CELL, 1993, 73 (01) : 35 - 46
  • [8] Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis
    Cudkowicz, ME
    McKennaYasek, D
    Sapp, PE
    Chin, W
    Geller, B
    Hayden, DL
    Schoenfeld, DA
    Hosler, BA
    Horvitz, HR
    Brown, RH
    [J]. ANNALS OF NEUROLOGY, 1997, 41 (02) : 210 - 221
  • [9] NEUROPATHOLOGICAL CHANGES IN 2 LINES OF MICE CARRYING A TRANSGENE FOR MUTANT HUMAN CU,ZN SOD, AND IN MICE OVEREXPRESSING WILD-TYPE HUMAN SOD - A MODEL OF FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS (FALS)
    DALCANTO, MC
    GURNEY, ME
    [J]. BRAIN RESEARCH, 1995, 676 (01) : 25 - 40
  • [10] PARVALBUMIN IS A MARKER OF ALS-RESISTANT MOTOR-NEURONS
    ELLIOTT, JL
    SNIDER, WD
    [J]. NEUROREPORT, 1995, 6 (03) : 449 - 452