Oligodendrocytes are critical for the development of the plasma membrane and cytoskeleton of the axon. In this paper, we show that fast axonal transport is also dependent on the oligodendrocyte. Using a mouse model of hereditary spastic paraplegia type 2 due to a null mutation of the myelin Plp gene, we find a progressive impairment in fast retrograde and anterograde transport. Increased levels of retrograde motor protein subunits are associated with accumulation of membranous organelles distal to nodal complexes. Using cell transplantation, we show categorically that the axonal phenotype is related to the presence of the overlying Plp null myelin. Our data demonstrate a novel role for oligodendrocytes in the local regulation of axonal function and have implications for the axonal loss associated with secondary progressive multiple sclerosis.
Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia
The online version of this article includes supplemental material.
D. Yool's present address is Dept. of Veterinary Clinical Studies, Royal (Dick) School of Veterinary Studies, Hospital for Small Animals, Easter Bush Veterinary Centre, Roslin EH25 9RG, Scotland, UK.
Abbreviations used in this paper: CTB, cholera toxin B subunit; HSP, hereditary spastic paraplegia; MBP, myelin basic protein; NF, neurofilament; PLP, proteolipid protein; RGC, retinal ganglion cell.
Julia M. Edgar, Mark McLaughlin, Donald Yool, Su-Chun Zhang, Jill H. Fowler, Paul Montague, Jennifer A. Barrie, Mailis C. McCulloch, Ian D. Duncan, James Garbern, Klaus A. Nave, Ian R. Griffiths; Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia . J Cell Biol 5 July 2004; 166 (1): 121–131. doi: https://doi.org/10.1083/jcb.200312012
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