Oligodendroglial modulation of fast axonal transport in a mouse model of hereditary spastic paraplegia

被引:242
作者
Edgar, JM
McLaughlin, M
Yool, D
Zhang, SC
Fowler, JH
Montague, P
Barrie, JA
McCulloch, MC
Duncan, ID
Garbern, J
Nave, KA
Griffiths, IR [1 ]
机构
[1] Univ Glasgow, Appl Neurobiol Grp, Dept Vet Clin Studies, Glasgow G61 1QH, Lanark, Scotland
[2] Univ Glasgow, Wellcome Surg Inst, Glasgow G61 1QH, Lanark, Scotland
[3] Univ Wisconsin, Dept Med Sci, Sch Vet Med, Madison, WI 53706 USA
[4] Wayne State Univ, Dept Neurol, Detroit, MI 48201 USA
[5] Wayne State Univ, Ctr Mol Med & Genet, Detroit, MI 48201 USA
[6] Max Planck Inst Expt Med, Dept Neurogenet, D-37075 Gottingen, Germany
关键词
proteolipid protein; oligodendrocyte; axonal transport; hereditary spastic paraplegia; axonal degeneration;
D O I
10.1083/jcb.200312012
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
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.
引用
收藏
页码:121 / 131
页数:11
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