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.
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1 November 1996
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November 01 1996
Neurofilament subunit NF-H modulates axonal diameter by selectively slowing neurofilament transport.
J R Marszalek,
J R Marszalek
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
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T L Williamson,
T L Williamson
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
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M K Lee,
M K Lee
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
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Z Xu,
Z Xu
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
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P N Hoffman,
P N Hoffman
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
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M W Becher,
M W Becher
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
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T O Crawford,
T O Crawford
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
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D W Cleveland
D W Cleveland
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
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J R Marszalek
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
T L Williamson
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
M K Lee
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
Z Xu
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
P N Hoffman
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
M W Becher
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
T O Crawford
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
D W Cleveland
Division of Cellular and Molecular Medicine, University of California at San Diego, La Jolla 92093, USA.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1996) 135 (3): 711–724.
Citation
J R Marszalek, T L Williamson, M K Lee, Z Xu, P N Hoffman, M W Becher, T O Crawford, D W Cleveland; Neurofilament subunit NF-H modulates axonal diameter by selectively slowing neurofilament transport.. J Cell Biol 1 November 1996; 135 (3): 711–724. doi: https://doi.org/10.1083/jcb.135.3.711
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