TY - JOUR
T1 - Myelin abnormalities in mice deficient in galactocerebroside and sulfatide
AU - Dupree, Jeffrey L.
AU - Coetzee, Timothy
AU - Suzuki, Kinuko
AU - Popko, Brian
N1 - Funding Information:
This work was supported by Grants NS27336 (B.P.) and NS24453 (K.S.) from the National Institutes of Health (NIH) and Mental Retardation Research Center Core Grant HD03110 from the NIH. J.D. and T.C. were supported by Advanced Postdoctoral Fellowships from the National Multiple Sclerosis Society. We thank Dr Robert Bagnell, Victoria Madden, and Clarita Langa-man for their assistance with the electron microscopic analysis and Dr Cedric Raine for his insightful critique of the electron micrographs.
PY - 1998
Y1 - 1998
N2 - Myelin sheath formation depends on appropriate axo-glial interactions that are mediated by myelin-specific surface molecules. In this study, we have used quantitative morphological analyses to determine the roles of the prominent myelin lipids galactocerebroside (GalC) and sulfatide in both central and peripheral myelin formation, exploiting mutant mice incapable of synthesizing these lipids. Our results demonstrate a significant increase in uncompacted myelin sheaths, the frequency of multiple cytoplasmic loops, redundant myelin profiles, and Schmidt-Lanterman incisures in the CNS of these mutant mice. In contrast, PNS myelin appeared structurally normal in these animals; however, at post-natal day 10, greater than 10% of the axons withered and pulled away from their myelin sheaths. These results indicate that GalC and sulfatide are critical to the formation of CNS myelin. In contrast, PNS myelin formation is not dependent on these lipids; however, GalC and sulfatide appear to be instrumental in maintaining Schwann cell- axon contact during a specific developmental window.
AB - Myelin sheath formation depends on appropriate axo-glial interactions that are mediated by myelin-specific surface molecules. In this study, we have used quantitative morphological analyses to determine the roles of the prominent myelin lipids galactocerebroside (GalC) and sulfatide in both central and peripheral myelin formation, exploiting mutant mice incapable of synthesizing these lipids. Our results demonstrate a significant increase in uncompacted myelin sheaths, the frequency of multiple cytoplasmic loops, redundant myelin profiles, and Schmidt-Lanterman incisures in the CNS of these mutant mice. In contrast, PNS myelin appeared structurally normal in these animals; however, at post-natal day 10, greater than 10% of the axons withered and pulled away from their myelin sheaths. These results indicate that GalC and sulfatide are critical to the formation of CNS myelin. In contrast, PNS myelin formation is not dependent on these lipids; however, GalC and sulfatide appear to be instrumental in maintaining Schwann cell- axon contact during a specific developmental window.
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U2 - 10.1023/A:1006908013972
DO - 10.1023/A:1006908013972
M3 - Article
C2 - 10447239
AN - SCOPUS:0032420901
SN - 0300-4864
VL - 27
SP - 649
EP - 659
JO - Journal of Neurocytology
JF - Journal of Neurocytology
IS - 9
ER -