Jan 2, 2011 FA2H and other enzymes are responsible for the increase in 2-OH very-long- chain (>C20) fatty acid contents in galactolipids during myelination.

Recent studies have found that mice lacking either the galactolipids or PLP are able to form myelin sheaths with apparently normal periodicity and The abnormal myelin structures present in the mutant animals are consistent with the possibility that the galactolipids play a role in regulating or mediating proper axo-glial interactions. The further detailed analysis of these animals should help refine our understanding of galactolipid function in the myelination process. Among the most abundant components of myelin are the galactolipids galactocerebroside (GalC) and sulfatide. In spite of this abundance, the roles that these molecules play in the myelin sheath are not well understood. The vertebrate myelin sheath is greatly enriched in the galactolipids galactocerebroside (GalC) and sulfatide. Mice with a disruption in the gene that encodes the biosynthetic enzyme UDP-galactose:ceramide galactosyl transferase (CGT) are incapable of synthesizing these lipids yet form myelin sheaths that exhibit major and minor dense lines with spacing comparable to controls.

Among the most abundant components of myelin are the galactolipids galactocerebroside (GalC) and sulfatide. In spite of this abundance, the roles that these molecules play in the myelin sheath are not well understood. The vertebrate myelin sheath is greatly enriched in the galactolipids galactocerebroside (GalC) and sulfatide. Mice with a disruption in the gene that encodes the biosynthetic enzyme UDP-galactose:ceramide galactosyl transferase (CGT) are incapable of synthesizing these lipids yet form myelin sheaths that exhibit major and minor dense lines with spacing comparable to controls. The galactolipids galactocerebroside and sulfatide and the proteolipid protein (PLP) and its splice variant DM20 are the most abundant lipid and protein components of central nervous system myelin. Recent studies have found that mice lacking either the galactolipids or PLP are able to form myelin sheaths with apparently normal periodicity and A defining feature of the vertebrate nervous system is the ensheathment of axons by myelin, a multilamellar membrane containing a small group of proteins and an abundance of the galactolipid galactocerebroside (GalC) and its sulfated derivative sulfatide. Several in vitro studies have suggested that these galactolipids transduce developmental signals, facilitate protein trafficking and TY - THES.

The abnormal myelin structures present in the mutant animals are consistent with the possibility that the galactolipids play a role in regulating or mediating proper axo-glial interactions. The further detailed analysis of these animals should help refine our understanding of galactolipid function in the myelination process.

increase rapidly during developmental myelination. CHANGES DURING EARLY MYELINATION 189 These two measures (Figs.

galactolipids, two glial components implicated in mediating axo-glial interactions during the myelination process. The single-mutant mice produce abnormal myelin containing similar ultrastructural abnormalities, suggesting that these molecules may play an overlapping role in myelin formation. Furthermore, the absence of the galactolipids

The vertebrate myelin sheath is greatly enriched in the galactolipids galactocerebroside (GalC) and sulfatide. Mice with a disruption in the gene that encodes the biosynthetic enzyme UDP-galactose:ceramide galactosyl transferase (CGT) are incapable of synthesizing these lipids yet form myelin sheaths that exhibit major and minor dense lines with spacing comparable to controls. Download Citation | Galactolipids are molecular determinants of myelin development and axo-glial organization | Myelination is a developmentally regulated process whereby myelinating glial cells A defining feature of the vertebrate nervous system is the ensheathment of axons by myelin, a multilamellar membrane containing a small group of proteins and an abundance of the galactolipid galactocerebroside (GalC) and its sulfated derivative sulfatide. In this study, we have tested for the possibility that MAG and myelin galactolipids function similarly in mediating early stages of myelination. Previous experiments, mainly cell culture based, have employed biochemical strategies to determine that MAG and the galactolipids are critical early mediators of myelin formation ( Dupree et al., 1998c ; Schachner and Bartsch, 2000 ).

Recently, the isolation of the gene that encodes UDP-galactose:ceramide Lipid rafts play critical The biochemical basis for the increase in 2-hydroxy roles in neural development (38), and a number of mye- galactolipids during myelination is now explained, at least lin proteins involved in cell signaling and adhesion are in part, by the upregulation of FA2H in oligodendrocytes associated with lipid rafts (39). The biochemical basis of the increase in 2-hydroxy galactolipids during myelination is now. explained, at least in part, by the upregulation of FA2H in oligodendrocytes and Schwann cells. The galactolipids galactocerebroside and sulfatide, which require the enzyme UDP‐galactose:ceramide galactosyltransferase (CGT) for their synthesis, are among the most prevalent molecules in the myelin sheath. Numerous studies, mainly using antibody perturbation methods in vitro, have suggested that these molecules are crucial mediators of oligodendrocyte differentiation and myelin formation galactolipids, two glial components implicated in mediating axo-glial interactions during the myelination process. The single-mutant mice produce abnormal myelin containing similar ultrastructural abnormalities, suggesting that these molecules may play an overlapping role in myelin formation.
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In this study, we have tested for the possibility that MAG and myelin galactolipids function similarly in mediating early stages of myelination. Previous experiments, mainly cell culture based, have employed biochemical strategies to determine that MAG and the galactolipids are critical early mediators of myelin formation ( Dupree et al., 1998c ; Schachner and Bartsch, 2000 ).

Novel oligodendrocyte transmembrane signaling systems. CHANGES DURING EARLY MYELINATION 189 These two measures (Figs. 3 and 4) show very similar developmental profiles in the forebrain as well as in the cerebellum, indicating their value as myelin markers.
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Galactolipids are a type of glycolipid whose sugar group is galactose.They differ from glycosphingolipids in that they do not have nitrogen in their composition.. They are the main part of plant membrane lipids where they substitute phospholipids to conserve phosphate for other essential processes. These chloroplast membranes contain a high quantity of monogalactosyldiacylglycerol (MGDG) and

The fatty acid compositions of galactolipids in neonatal mouse brain gradually changed during the course of myelination. The relative ratio of 2-hydroxy versus nonhydroxy galactolipids was very low at 2 days of age (∼8% of total galactolipids) and increased 6- to 8-fold by 30 days of age. Lipid hydroxylation in glial cell signaling and myelination Hama, Hiroko Medical University of South Carolina, Charleston, SC, United States. Search 17 grants MYELIN is the most stable membrane known and the fact that it contains ten times as much long chain sphingolipid as any other known membrane structure has led to the suggestion that the long chain fatty acids (> 18 carbon atoms) in these sphingolipids are concerned in the stability of myelin^1,2. The finding^3,4 of a myelin deficient mouse mutant whose galactolipids and Despite the extraordinary abundance of 2-OH galactolipids in myelin, there is surprisingly little understanding of the basic biochemistry and physiological role of 2-OH galactolipids.