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
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