Marszalek J R, Williamson T L, Lee M K, Xu Z, Hoffman P N, Becher M W, Crawford T O, Cleveland D W
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
J Cell Biol. 1996 Nov;135(3):711-24. doi: 10.1083/jcb.135.3.711.
To examine the mechanism through which neurofilaments regulate the caliber of myelinated axons and to test how aberrant accumulations of neurofilaments cause motor neuron disease, mice have been constructed that express wild-type mouse NF-H up to 4.5 times the normal level. Small increases in NF-H expression lead to increased total neurofilament content and larger myelinated axons, whereas larger increases in NF-H decrease total neurofilament content and strongly inhibit radial growth. Increasing NF-H expression selectively slow neurofilament transport into and along axons, resulting in severe perikaryal accumulation of neurofilaments and proximal axonal swellings in motor neurons. Unlike the situation in transgenic mice expressing modest levels of human NF-H (Cote, F., J.F. Collard, and J.P. Julien. 1993. Cell. 73:35-46), even 4.5 times the normal level of wild-type mouse NF-H does not result in any overt phenotype or enhanced motor neuron degeneration or loss. Rather, motor neurons are extraordinarily tolerant of wild-type murine NF-H, whereas wild-type human NF-H, which differs from the mouse homolog at > 160 residue positions, mediates motor neuron disease in mice by acting as an aberrant, mutant subunit.
为了研究神经丝调节有髓轴突管径的机制,并测试神经丝异常聚集如何导致运动神经元疾病,已构建出表达野生型小鼠NF-H的水平高达正常水平4.5倍的小鼠。NF-H表达的小幅增加会导致神经丝总含量增加以及有髓轴突变大,而NF-H表达的大幅增加则会降低神经丝总含量并强烈抑制径向生长。增加NF-H表达会选择性地减缓神经丝向轴突内及沿轴突的运输,导致运动神经元中神经丝在核周严重聚集以及近端轴突肿胀。与表达适度水平人类NF-H的转基因小鼠的情况不同(科特,F.,J.F. 科拉德,和J.P. 朱利安。1993年。《细胞》。73:35 - 46),即使野生型小鼠NF-H的水平达到正常水平的4.5倍也不会导致任何明显的表型或运动神经元变性或丢失加剧。相反,运动神经元对野生型小鼠NF-H具有极强的耐受性,而与小鼠同源物在超过160个残基位置存在差异的野生型人类NF-H,通过作为异常的突变亚基在小鼠中介导运动神经元疾病。