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Science 5 June 1998:
Vol. 280. no. 5369, pp. 1610 - 1613
DOI: 10.1126/science.280.5369.1610

Reports

Axonal Swellings and Degeneration in Mice Lacking the Major Proteolipid of Myelin

Ian Griffiths, Matthias Klugmann, Thomas Anderson, Donald Yool, Christine Thomson, Markus H. Schwab, Armin Schneider, Frank Zimmermann, Mailise McCulloch, Nancy Nadon, Klaus-Armin Nave *

Glial cells produce myelin and contribute to axonal morphology in the nervous system. Two myelin membrane proteolipids, PLP and DM20, were shown to be essential for the integrity of myelinated axons. In the absence of PLP-DM20, mice assembled compact myelin sheaths but subsequently developed widespread axonal swellings and degeneration, associated predominantly with small-caliber nerve fibers. Similar swellings were absent in dysmyelinated shiverer mice, which lack myelin basic protein (MBP), but recurred in MBP*PLP double mutants. Thus, fiber degeneration, which was probably secondary to impaired axonal transport, could indicate that myelinated axons require local oligodendroglial support.

I. Griffiths, T. Anderson, D. Yool, C. Thomson, M. McCulloch, Applied Neurobiology Group, Department of Veterinary Clinical Studies, University of Glasgow, Glasgow G61 1QH, Scotland, UK.
M. Klugmann, M. H. Schwab, A. Schneider, F. Zimmerman, K.-A. Nave, Zentrum für Molekulare Biologie (ZMBH), Universität Heidelberg, Im Neuenheimer Feld 282, D-69120 Heidelberg, Germany.
N. Nadon, Oklahoma Medical Research Foundation, 825 Northeast 13th Street, Oklahoma City, OK 73104, USA.
*   To whom correspondence should be addressed. E-mail: nave{at}sun0.urz.uni-heidelberg.de


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   Abstract »    Full Text »    PDF »
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