NF-M is an essential target for the myelin-directed “outside-in” signaling cascade that mediates radial axonal growth
Open Access
- 8 December 2003
- journal article
- research article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 163 (5) , 1011-1020
- https://doi.org/10.1083/jcb.200308159
Abstract
Neurofilaments are essential for acquisition of normal axonal calibers. Several lines of evidence have suggested that neurofilament-dependent structuring of axoplasm arises through an “outside-in” signaling cascade originating from myelinating cells. Implicated as targets in this cascade are the highly phosphorylated KSP domains of neurofilament subunits NF-H and NF-M. These are nearly stoichiometrically phosphorylated in myelinated internodes where radial axonal growth takes place, but not in the smaller, unmyelinated nodes. Gene replacement has now been used to produce mice expressing normal levels of the three neurofilament subunits, but which are deleted in the known phosphorylation sites within either NF-M or within both NF-M and NF-H. This has revealed that the tail domain of NF-M, with seven KSP motifs, is an essential target for the myelination-dependent outside-in signaling cascade that determines axonal caliber and conduction velocity of motor axons.Keywords
This publication has 55 references indexed in Scilit:
- The p75 Neurotrophin Receptor Interacts with Multiple MAGE ProteinsJournal of Biological Chemistry, 2002
- p75 interacts with the Nogo receptor as a co-receptor for Nogo, MAG and OMgpNature, 2002
- Neurofilament subunit NF-H modulates axonal diameter by selectively slowing neurofilament transport.The Journal of cell biology, 1996
- Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosisNature, 1995
- Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: A mouse model of amyotrophic lateral sclerosisCell, 1993
- Assembly properties of dominant and recessive mutations in the small mouse neurofilament (NF-L) subunit.The Journal of cell biology, 1990
- The expression and posttranslational modification of a neuron‐specific β‐tubulin isotype during chick embryogenesisCell Motility, 1990
- Plectin: General Overview and Appraisal of its potential Role as a Subunit Protein of the CytomatriCritical Reviews in Biochemistry and Molecular Biology, 1989
- Structure of the peripheral domains of neurofilaments revealed by low angle rotary shadowingJournal of Molecular Biology, 1988
- In vivo microtubules are copolymers of available beta-tubulin isotypes: localization of each of six vertebrate beta-tubulin isotypes using polyclonal antibodies elicited by synthetic peptide antigens.The Journal of cell biology, 1987