Myelination in the absence of galactocerebroside and sulfatide: Normal structure with abnormal function and regional instability

被引:515
作者
Coetzee, T
Fujita, N
Dupree, J
Shi, R
Blight, A
Suzuki, K
Suzuki, K
Popko, B
机构
[1] UNIV N CAROLINA,DEPT PATHOL & LAB MED,CHAPEL HILL,NC 27599
[2] UNIV N CAROLINA,DEPT SURG,DIV NEUROSURG,CHAPEL HILL,NC 27599
[3] UNIV N CAROLINA,DEPT NEUROL & PSYCHIAT,CHAPEL HILL,NC 27599
[4] UNIV N CAROLINA,DEPT BIOCHEM & BIOPHYS,CHAPEL HILL,NC 27599
[5] UNIV N CAROLINA,PROGRAM MOL BIOL & BIOTECHNOL,CHAPEL HILL,NC 27599
关键词
D O I
10.1016/S0092-8674(00)80093-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The vertebrate nervous system is characterized by ensheathment of axons with myelin, a multilamellar membrane greatly enriched in the galactolipid galactocerebroside (GalC) and its sulfated derivative sulfatide. We have generated mice lacking the enzyme UDP-galactose:ceramide galactosyltransferase (CGT), which is required for GalC synthesis. CGT-deficient mice do not synthesize GalC or sulfatide but surprisingly form myelin containing glucocerebroside, a lipid not previously identified in myelin. Microscopic and morphometric analyses revealed myelin of normal ultrastructural appearance, except for slightly thinner sheaths in the ventral region of the spinal cord. Nevertheless, these mice exhibit severe generalized tremoring and mild ataxia, and electrophysiological analysis showed conduction deficits consistent with reduced insulative capacity of the myelin sheath. Moreover, with age, CGT-deficient mice develop progressive hindlimb paralysis and extensive vacuolation of the ventral region of the spinal cord. These results indicate that GalC and sulfatide play important roles in myelin function and stability.
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页码:209 / 219
页数:11
相关论文
共 65 条
[1]  
ABRAMSON MB, 1965, J BIOL CHEM, V240, P2389
[2]   ELECTRON MICROSCOPIC AND ENZYME HISTOCHEMICAL STUDIES OF CEREBELLUM IN SPONGY DEGENERATION - (VAN BOGAERT AND BERTRAND TYPE) [J].
ADACHI, M ;
SCHNECK, L ;
VOLK, BW ;
TORII, J .
ACTA NEUROPATHOLOGICA, 1972, 20 (01) :22-&
[3]   HYPERMYELINATION AND DEMYELINATING PERIPHERAL NEUROPATHY IN PMP22-DEFICIENT MICE [J].
ADLKOFER, K ;
MARTINI, R ;
AGUZZI, A ;
ZIELASEK, J ;
TOYKA, KV ;
SUTER, U .
NATURE GENETICS, 1995, 11 (03) :274-280
[4]   FINE STRUCTURE AND ELECTROLYTE ANALYSIS OF CEREBRAL EDEMA INDUCED BY ALKYL TIN INTOXICATION [J].
ALEU, FP ;
KATZMAN, R ;
TERRY, RD .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1963, 22 (03) :403-&
[5]  
[Anonymous], EXPT CLIN NEUROTOXIC
[6]   REVERSIBLE INHIBITION OF OLIGODENDROCYTE PROGENITOR DIFFERENTIATION BY A MONOCLONAL-ANTIBODY AGAINST SURFACE GALACTOLIPIDS [J].
BANSAL, R ;
PFEIFFER, SE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (16) :6181-6185
[7]   INTRACELLULAR-RECORDING FROM VERTEBRATE MYELINATED AXONS - MECHANISM OF THE DEPOLARIZING AFTERPOTENTIAL [J].
BARRETT, EF ;
BARRETT, JN .
JOURNAL OF PHYSIOLOGY-LONDON, 1982, 323 (FEB) :117-144
[8]  
BEAUDET AL, 1995, METABOLIC MOL BASIS, P4599
[9]  
BENJAMINS JA, 1990, ANN NY ACAD SCI, V305, P90
[10]   ION CHANNEL ORGANIZATION OF THE MYELINATED FIBER [J].
BLACK, JA ;
KOCSIS, JD ;
WAXMAN, SG .
TRENDS IN NEUROSCIENCES, 1990, 13 (02) :48-54