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Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase gene
Lipids in Health and Disease volume 5, Article number: 21 (2006)
Arylsulfatase A (ASA)-deficient mice are a model for the lysosomal storage disorder metachromatic leukodystrophy. This lipidosis is characterised by the lysosomal accumulation of the sphingolipid sulfatide. Storage of this lipid is associated with progressive demyelination. We have mated ASA-deficient mice with mice heterozygous for a non-functional allele of UDP-galactose:ceramide-galactosyltransferase (CGT). This deficiency is known to lead to a decreased synthesis of galactosylceramide and sulfatide, which should reduce sulfatide storage and improve pathology in ASA-deficient mice.
ASA-/- CGT+/- mice, however, showed no detectable decrease in sulfatide storage. Neuronal degeneration of cells in the spiral ganglion of the inner ear, however, was decreased. Behavioural tests showed small but clear improvements of the phenotype in ASA-/- CGT+/- mice.
Thus the reduction of galactosylceramide and sulfatide biosynthesis by genetic means overall causes modest improvements of pathology.
Metachromatic leukodystrophy (MLD) is a lysosomal storage disease of humans, which is characterised by progressive demyelination. The underlying defect is the deficiency of arylsulfatase A (ASA), which results in the lysosomal accumulation of the sphingolipid 3-O-sulfogalactosylceramide (sulfatide) predominantly in brain, kidney and bile ducts . In the typical late infantile form of the disease patients start to develop gait disturbances, ataxia and paresis between the ages of 18 to 24 months. The neurologic symptoms usually progress rapidly and finally patients die in a decerebrated state. The disease is currently untreatable. Since MLD naturally only occurs in humans a mouse model was generated by targeted disruption of the ASA gene . These animals store sulfatide in the same tissues as humans, including oligodendrocytes, Schwann cells and various neurons [2–4]. The accumulation of sulfatide in the central nervous system steadily increases with progressing age of the animals. However, the ASA-deficient mice have a mild phenotype, since they do not show widespread demyelination in the central nervous system typical for patients. Except for oligodendrocytes sulfatide is also stored in certain neurons, which in some cases leads to neuronal degeneration. This is particularly evident in the inner ear. In between 6 to 12 months of age neurons of the spiral ganglion of the inner ear degenerate completely [5, 6]. In addition, ASA-deficient mice show a decrease of the axonal diameter in peripheral nerves [2, 7]. The mice develop progressive neurological symptoms, which are, however, not lethal. In summary, the pathological and behavioural studies performed so far suggest that the animals resemble early stages of human disease [2, 3, 8–10].
Sulfatide is synthesised by sulfation of its precursor galactosylceramide which is formed from ceramide by catalysis of the enzyme UDP-galactose:ceramide-galactosyltransferase (CGT). Mice deficient for this enzyme do not produce galactosylceramide nor sulfatide [11, 12]. Surprisingly, they are still able to myelinate since they compensatorily synthesise glucosylceramide . They develop various neurologic symptoms and die at the age of 2 to 3 months [11–14]. Heterozygous littermates having only one copy of the CGT gene were investigated up to the age of three months. They do not show any pathological phenotype but display reduced levels of galactosylceramide as well as sulfatide [12, 13]. In these studies galactosylceramide was found to be reduced to about 70–80% and sulfatide to about 80% of normal, respectively.
To investigate whether reduction of galactosylceramide synthesis is an option to treat MLD, CGT-heterozygous animals were mated with ASA-deficient mice to obtain ASA-/- CGT+/- animals. The influence of CGT heterozygosity on the phenotype of ASA-deficient mice was examined.
Brain lipid analysis of ASA-deficient mice heterozygous for a non-functional CGT allele
To investigate whether a decrease in galactosylceramide and sulfatide synthesis can improve the phenotype of ASA-deficient mice we crossed ASA-/- with CGT+/- mice. Genotypes of offspring at the ASA and CGT locus were determined by PCR as described under material and methods. Lipids were extracted from brains of mice with different genotypes and galactosylceramide and sulfatide were quantified by thin layer chromatography (see Figure 1). Compared to control animals (ASA+/+ CGT+/+) levels of sulfatide were increased in ASA-deficient animals but no significant difference was found between ASA-deficient mice with CGT+/+ and CGT+/- genetic background. Galactosylceramide levels are decreased in brains of MLD patients and ASA-deficient mice. This was also found in the mice investigated here and again no difference was found between CGT+/+ and CGT+/- mice. Thus, the alteration in CGT gene dosage has no obvious overall effect on sulfatide accumulation and galactosylceramide reduction in brains of ASA-deficient mice.
Pathology of ASA-deficient mice heterozygous for a non-functional CGT allele
Beside the nervous system kidneys of ASA-deficient mice show the highest amount of sulfatide storage material . The histochemical examination of the kidneys revealed no differences between ASA-/- CGT +/- mice and ASA-/- CGT+/+ mice, as far as the degree and topographic distribution of sulfatide storage are concerned (results not shown). In the nervous system the most impressive degenerative alteration seen in ASA-deficient mice is the neuronal cell loss in the spiral ganglion of the inner ear starting 6 – 8 months after birth. At the age of 12 months the majority of neurons is lost in ASA-deficient mice [5, 6]. To examine whether the heterozygosity for CGT has any influence on the pathology of ASA-deficient mice we quantified the cell loss in the spiral ganglion of mice with various genotypes. In these examinations ASA-deficient mice bearing only one intact CGT gene showed a clear improvement of pathology (see figure 2). The degeneration of neurons observed in the spiral ganglion of ASA-deficient mice was clearly mitigated in the CGT-heterozygous mice. This improvement can easily be seen by light microscopy (Fig. 2). We also quantified the number of cells by counting cells present in an area of defined size. This revealed a remarkable difference between ASA-/- CGT+/+ and ASA-/- CGT+/- mice. In animals older than 12 month only 26% of cells had survived in the spiral ganglion of ASA-deficient mice when compared to wild-type, whereas 57% were still structurally intact in mice bearing only one intact CGT gene (Figure 2d).
ASA-deficient mice show various slowly progressing neurologic symptoms. The animals are hyperactive, have problems to stay on a rotating rod and show impairment in the morris water maze . In the latter, however, impairments may be due to reduced neuromotor coordination capabilities rather than true learning deficits. To examine whether behavioural impairments are improved in ASA-/- CGT+/- mice, we performed various behavioural tests with these animals. When compared to wild-type and ASA-deficient mice no significant improvement in cage activity, rotarod or open field testing could be observed in ASA-deficient animals heterozygous for CGT. Only the Dark-Light-transition box test – a test of exploration and anxiety, but possibly less affected by the hyperactivity of the animals – showed a significant improvement in ASA-deficient mice bearing only one CGT allele (fig. 3).
In recent years various approaches to treat lysosomal storage diseases have been investigated. These include enzyme replacement therapy, gene therapy and substrate reduction therapy. Enzyme replacement therapy has been approved as therapy for various lysosomal storage diseases, such as Gaucher disease, Fabry disease, Pompe disease and certain kinds of mucopolysaccharidosis (for reviews see [16–20]). A number of reports deal with gene therapy approaches in animal models of lysosomal storage diseases [21–25]. However, although some of these studies show promising results the routine clinical application is not feasible in foreseeable future. In contrast, substrate reduction therapy has been shown to be a promising concept and is an approved therapy of some patient with Gaucher type 1 disease [26–31]. Compared to enzyme replacement, substrate reduction therapy may offer advantages for diseases with central nervous system involvement, because inhibition of synthesising enzymes depends on small molecule competitive inhibitors, which may be modified such that they can cross the blood brain barrier. In addition, treatment of hypercholesteremia with inhibitors of HMG-CoA-Reductase has proven that inhibition of lipid synthesis is a valuable clinical option to reduce levels of particular lipids [32, 33]. The compound N-butyldeoxynojirimycin has been shown to inhibit the synthesis of glucosylceramide and is approved for therapy of Gaucher disease in which glucosylceramide accumulates . Since glucosylceramide is also the precursor of gangliosides it is also employed in the treatment of GM2 gangliosidosis. The possible benefits of such a therapy has been demonstrated in animal models and clinical studies are already performed [31, 35–40].
Whereas globoid cell leukodystrophy (Krabbe disease) is the result of defects in the degradation of galactosylceramide, sulfatide accumulation leads to MLD. Thus, the inhibition of either CGT or galactosylceramide sulfotransferase (CST) is therefore an option to reduce galactosylceramide and/or sulfatide levels in these lysosomal storage disorders. Galactosylceramide storing twitcher mice, a model for Krabbe disease, show a decreased life span and body weight, and they suffer from demyelination and various neurological symptoms [41–43]. To investigate the possible benefits of reduction of galactosylceramide synthesis for the treatment of Krabbe disease, twitcher mice were mated with mice bearing a deficient CGT allele to yield twitcher mice with only one copy of a functional CGT allele. Although the amount of galactosylceramide was not reduced in the CGT-heterozygous twitcher mice these animals showed a moderate but significant improvement of their phenotype .
In MLD sulfatide is the accumulating lipid, and patients suffer from demyelination and devastating neurologic symptoms . Since the synthesis of sulfatide from ceramide is a two-step process both the enzymes involved – the CGT and the CST – are possible targets for inhibition of sulfatide synthesis. In contrast to glucosylceramide transferase, inhibitors of CGT or CST are currently not available. It was shown recently that mice bearing only one functional copy of the CGT gene have reduced levels of galactosylceramide as well as sulfatide [11, 12]. Therefore we mated these animals with ASA-deficient mice. In the CGT-heterozygous ASA-deficient mice, however, the overall amount of sulfatide in brain was not reduced. In addition no effect on the reduction of galactosylceramide in ASA-deficient mice was seen in the animals heterozygous for CGT. This is in accordance with the results presented for CGT-heterozygous twichter mice . Here also no reduction of galactosylceramide was found. In this study the authors interpreted this surprising results as coincidental. They assumed that the expected reduction in galactosylceramide is compensated by a prolonged survival of oligodendrocytes due to reduced galactosylceramide synthesis. As a consequence of reduced synthesis and preservation of oligodendrocytes the galactosylceramide levels appeared unaltered.
Beside lysosomal storage of sulfatide in myelin forming glia cells, examination of ASA-deficient mice has clearly shown, that also a number of neurons store sulfatide [2–4]. In neurons of the spiral ganglion this storage is accompanied with neuronal degeneration, whereas neuronal storage without any cellular damage can be observed in several nuclei of brainstem, diencephalon and spinal cord [2, 4]. Thus, the pathogenesis of this lysosomal storage disorder beside its glial certainly also has a neuronal component. For the spiral ganglion we found that the manipulation of galactosylceramide and sulfatide biosynthesis leads to mitigation of neuronal degeneration, although ganglion cells still do store sulfatides (Fig. 2c). Former experiments have demonstrated that brain stem auditory-evoked potentials correlate with the amounts of neurons in the spiral ganglion . Therefore we expect an improvement of the deafness phenotype seen in ASA-deficient mice. Unfortunately, due to the small number of neurons in this ganglion, we are not able to determine the extent of sulfatide storage at the cellular level, so that this improvement cannot directly be correlated with the accumulated amount of sulfatide.
The behavioural studies revealed only very selective improvements in ASA-deficient CGT-heterozygous mice. Thus, the phenotypic and pathologic improvements in ASA-/- CGT+/- mice are significant but overall minor. If extrapolated to the clinical situation they are certainly not satisfactory. However, it should be taken into account that the reduction of sulfatide biosynthesis in CGT+/- mice is only around 20%. The results presented here suggest that a far more efficient inhibition is necessary to achieve a substantial positive clinical effect. Surprisingly, this slight reduction is obviously already sufficient to mitigate the neuronal degeneration in the ASA-deficient mice.
Silica gel 60 (230–400 mesh) and precoated HPTLC-plates were obtained from Merck AG, Darmstadt, Germany. The silica-gel plates used for TLC-ELISA were precoated plastic sheets, Polygram R. Sil G, from Macherey-Nagel, Düringen, Germany. Sulfatide and galactosylceramide standards were isolated and characterised at the Institute of Clinical Neuroscience, Goteborg University, Sweden.
Generation of mice
Mice heterozygous for the CGT gene were a generous gift of B. Popko . For generation of CGT +/+ and CGT +/- on wildtype and ASA-deficient background the CGT heterozygous (C57/Bl6) animals were bred with wildtype as well as ASA-deficient (both 129ola). CGT +/+ and +/- littermates on the different ASA backgrounds were used for analysis.
For the genotyping of animals DNA of mouse tail tips was analysed by PCR using the following primers: 5'-TGACCAAGGCCTTGTTCCCAT-3', 5'-TAGGGTGGAAGTTACCCTAGA-3', 5'-GGAGAGGCTATTCGGCTATGAC-3' for ASA genotyping and 5'-CTCTCAGAAGGCAGAGACATTGCC-3', 5'-CATCCATAGGCTGGACCCATGAAC-3', 5'-GGAGAGGCTATTCGGCTATGAC-3' for CGT genotyping;
The PCR program was as follows: initial denaturation at 94°C for 5 min, then 32 cycles 94°C 30 s, 56°C 60 s, 72°C 120 s.
For ASA PCR resulted in a 480 bp product for the wild-type allele and a 1.2 kb for the knockout allele and for CGT in a 558 bp and a 1.4 kb product, respectively.
Lipid extraction and isolation
Frozen brains were mortared under liquid nitrogen and approximately 100 mg of the homogenised brain powder was processed for lipid extraction with chloroform:methanol:water, (C/M/W 4:8:3, by vol.) . Phase partition was performed in C/M/0.1 M KCl (10:5:2, by vol.). The final lipid fraction, consisting of the lower phase, was stored in C/M/W (60:30:4,5 by vol.) and aliquots of each age were taken for sulfatide and galactosylceramide determination by densitometry after High Performance Thin Layer Chromatography and orcinol visualisation . Significance of differences between means was assessed by 1-way ANOVA.
For the morphological examination animals 10 to 21 months of age were used. Some tissue samples of wild-type mice were taken from previous experiments. Under deep anaesthesia (intraperitoneal injection of tribromoethanol) the animals were killed by transcardial vascular perfusion with Bouin's mixture (diluted with phosphate-buffered saline to 25% of the original formula) or 6% glutaraldehyde in 0.1 M phosphate buffer (pH 7.4). Temporal bones were removed from the skull and decalcified with 4% EDTA . Bones and thick slices of kidneys were processed for selective staining of sulfatides. This was achieved by incubation (3 weeks) with the cationic dye alcian blue (Alcec Blue, Aldrich, Steinheim, Germany) in the presence of 0.3 M MgCl2 as described . The samples were then postfixed with 2% OsO4 for 3 hours and embedded in paraffin; sections (3–5 μm) were mounted with DePeX without further staining. Morphometric analysis of the spiral ganglion of the inner ear was performed by counting the ganglion cells in a test area measuring 120 μm × 120 μm. Significance of differences between means was assessed by 1-way ANOVA.
Behavioural testings were performed as already described .
For cage activity recording mice are on a 12/12 h dark-light schedule (lights on at 8 AM, off at 8 PM). Standard transparent mouse cages (16 × 22 cm2 bottom area; on sawdust bedding) are placed between 3 infrared photocells (2 along the short axis and 1 along the long axis of the cage), and the number of beam crossings is recorded during a defined period using a lab-built programmable counter. Single animals are placed in the recording cages in the late afternoon (dusk phase of their activity), and typically show an initial increase of exploratory activity followed by relatively high nocturnal activity. Activity is thus expressed as total beam crossings during the first 2 h as well as during the total 16 h overnight recording (4 PM through 8 AM).
Exploratory activity is assessed in the dark-light transition box. The box consists of a large illuminated compartment (55 × 73 cm2) and a smaller dark compartment (9 × 73 cm2) with four 4-cm holes, equally spaced in the dividing wall to allow transition between these compartments. Mice are first dark adapted for 1 h, and subsequently, placed in the dark compartment of the box. Exploratory activity is recorded for 10 min and expressed as the amount of crossings of 2 photobeams parallel to the dividing wall (beam 1: 1 cm from the wall; beam 2: 10 cm from the wall).
Significance of differences between means was assessed by 1-way ANOVA.
von Figura K, Gieselmann V, Jaeken J: Metachromatic leukodystrophy. The metabolic and molecular bases of inherited disease. Edited by: Scriver CR BALSWSVD. 2001, 3: 3695-3724. New York , McGraw-Hill Professional Publishing, 8th
Hess B, Saftig P, Hartmann D, Coenen R, Lullmann-Rauch R, Goebel HH, Evers M, von Figura K, D'Hooge R, Nagels G, De Deyn P, Peters C, Gieselmann V: Phenotype of arylsulfatase A-deficient mice: relationship to human metachromatic leukodystrophy. Proc Natl Acad Sci U S A. 1996, 93 (25): 14821-14826. 10.1073/pnas.93.25.14821
Gieselmann V, Matzner U, Hess B, Lullmann-Rauch R, Coenen R, Hartmann D, D'Hooge R, DeDeyn P, Nagels G: Metachromatic leukodystrophy: molecular genetics and an animal model. J Inherit Metab Dis. 1998, 21 (5): 564-574. 10.1023/A:1005471106088
Wittke D, Hartmann D, Gieselmann V, Lullmann-Rauch R: Lysosomal sulfatide storage in the brain of arylsulfatase A-deficient mice: cellular alterations and topographic distribution. Acta Neuropathol (Berl). 2004, 108 (4): 261-271. 10.1007/s00401-004-0883-6
Coenen R, Gieselmann V, Lullmann-Rauch R: Morphological alterations in the inner ear of the arylsulfatase A-deficient mouse. Acta Neuropathol (Berl). 2001, 101 (5): 491-498.
D'Hooge R, Coenen R, Gieselmann V, Lullmann-Rauch R, De Deyn PP: Decline in brainstem auditory-evoked potentials coincides with loss of spiral ganglion cells in arylsulfatase A-deficient mice. Brain Res. 1999, 847 (2): 352-356. 10.1016/S0006-8993(99)02085-5
Matzner U, Hartmann D, Lullmann-Rauch R, Coenen R, Rothert F, Mansson JE, Fredman P, D'Hooge R, De Deyn PP, Gieselmann V: Bone marrow stem cell-based gene transfer in a mouse model for metachromatic leukodystrophy: effects on visceral and nervous system disease manifestations. Gene Ther. 2002, 9 (1): 53-63. 10.1038/sj.gt.3301593
D'Hooge R, Franck F, Mucke L, De Deyn PP: Age-related behavioural deficits in transgenic mice expressing the HIV-1 coat protein gp120. Eur J Neurosci. 1999, 11 (12): 4398-4402. 10.1046/j.1460-9568.1999.00857.x
D'Hooge R, Hartmann D, Manil J, Colin F, Gieselmann V, De Deyn PP: Neuromotor alterations and cerebellar deficits in aged arylsulfatase A-deficient transgenic mice. Neurosci Lett. 1999, 273 (2): 93-96. 10.1016/S0304-3940(99)00647-3
D'Hooge R, Van Dam D, Franck F, Gieselmann V, De Deyn PP: Hyperactivity, neuromotor defects, and impaired learning and memory in a mouse model for metachromatic leukodystrophy. Brain Res. 2001, 907 (1-2): 35-43. 10.1016/S0006-8993(01)02374-5
Bosio A, Binczek E, Stoffel W: Functional breakdown of the lipid bilayer of the myelin membrane in central and peripheral nervous system by disrupted galactocerebroside synthesis. Proc Natl Acad Sci U S A. 1996, 93 (23): 13280-13285. 10.1073/pnas.93.23.13280
Coetzee T, Fujita N, Dupree J, Shi R, Blight A, Suzuki K, Popko B: Myelination in the absence of galactocerebroside and sulfatide: normal structure with abnormal function and regional instability. Cell. 1996, 86 (2): 209-219. 10.1016/S0092-8674(00)80093-8
Bosio A, Binczek E, Haupt WF, Stoffel W: Composition and biophysical properties of myelin lipid define the neurological defects in galactocerebroside- and sulfatide-deficient mice. J Neurochem. 1998, 70 (1): 308-315.
Coetzee T, Dupree JL, Popko B: Demyelination and altered expression of myelin-associated glycoprotein isoforms in the central nervous system of galactolipid-deficient mice. J Neurosci Res. 1998, 54 (5): 613-622. 10.1002/(SICI)1097-4547(19981201)54:5<613::AID-JNR6>3.0.CO;2-V
Lullmann-Rauch R, Matzner U, Franken S, Hartmann D, Gieselmann V: Lysosomal sulfoglycolipid storage in the kidneys of mice deficient for arylsulfatase A (ASA) and of double-knockout mice deficient for ASA and galactosylceramide synthase. Histochem Cell Biol. 2001, 116 (2): 161-169.
Schiffmann R, Brady RO: New prospects for the treatment of lysosomal storage diseases. Drugs. 2002, 62 (5): 733-742. 10.2165/00003495-200262050-00002
Siatskas C, Medin JA: Gene therapy for Fabry disease. J Inherit Metab Dis. 2001, 24 Suppl 2: 25-41; discussion 11-2. 10.1023/A:1012455421014
Hodges BL, Cheng SH: Cell and gene-based therapies for the lysosomal storage diseases. Curr Gene Ther. 2006, 6 (2): 227-241. 10.2174/156652306776359522
Miebach E: Enzyme replacement therapy in mucopolysaccharidosis type I. Acta Paediatr Suppl. 2005, 94 (447): 58-60; discussion 57. 10.1080/08035320510028120
Pastores GM, Thadhani R: Advances in the management of Anderson-Fabry disease: enzyme replacement therapy. Expert Opin Biol Ther. 2002, 2 (3): 325-333. 10.1517/147125188.8.131.525
Sands MS, Davidson BL: Gene therapy for lysosomal storage diseases. Mol Ther. 2006, 13 (5): 839-849. 10.1016/j.ymthe.2006.01.006
Matzner U, Gieselmann V: Gene therapy of metachromatic leukodystrophy. Expert Opin Biol Ther. 2005, 5 (1): 55-65. 10.1517/147125184.108.40.206
Biffi A, Naldini L: Gene therapy of storage disorders by retroviral and lentiviral vectors. Hum Gene Ther. 2005, 16 (10): 1133-1142. 10.1089/hum.2005.16.1133
Eto Y, Shen JS, Meng XL, Ohashi T: Treatment of lysosomal storage disorders: cell therapy and gene therapy. J Inherit Metab Dis. 2004, 27 (3): 411-415. 10.1023/B:BOLI.0000031170.69676.68
Ellinwood NM, Vite CH, Haskins ME: Gene therapy for lysosomal storage diseases: the lessons and promise of animal models. J Gene Med. 2004, 6 (5): 481-506. 10.1002/jgm.581
Bembi B, Marchetti F, Guerci VI, Ciana G, Addobbati R, Grasso D, Barone R, Cariati R, Fernandez-Guillen L, Butters T, Pittis MG: Substrate reduction therapy in the infantile form of Tay-Sachs disease. Neurology. 2006, 66 (2): 278-280. 10.1212/01.wnl.0000194225.78917.de
Jmoudiak M, Futerman AH: Gaucher disease: pathological mechanisms and modern management. Br J Haematol. 2005, 129 (2): 178-188. 10.1111/j.1365-2141.2004.05351.x
Cox TM: Substrate reduction therapy for lysosomal storage diseases. Acta Paediatr Suppl. 2005, 94 (447): 69-75; discussion 57. 10.1080/08035320510028157
Butters TD, Dwek RA, Platt FM: Imino sugar inhibitors for treating the lysosomal glycosphingolipidoses. Glycobiology. 2005, 15 (10): 43R-52R. 10.1093/glycob/cwi076
Moyses C: Substrate reduction therapy: clinical evaluation in type 1 Gaucher disease. Philos Trans R Soc Lond B Biol Sci. 2003, 358 (1433): 955-960. 10.1098/rstb.2003.1271
Butters TD, Dwek RA, Platt FM: New therapeutics for the treatment of glycosphingolipid lysosomal storage diseases. Adv Exp Med Biol. 2003, 535: 219-226.
Rodenburg J, Vissers MN, Daniels SR, Wiegman A, Kastelein JJ: Lipid-lowering medications. Pediatr Endocrinol Rev. 2004, 2 Suppl 1: 171-180.
Vaughan CJ, Gotto AMJ: Update on Statins: 2003. Circulation. 2004, 110 (7): 886- 10.1161/01.CIR.0000139312.10076.BA
Platt FM, Neises GR, Dwek RA, Butters TD: N-butyldeoxynojirimycin is a novel inhibitor of glycolipid biosynthesis. J Biol Chem. 1994, 269 (11): 8362-8365.
Weinreb NJ, Barranger JA, Charrow J, Grabowski GA, Mankin HJ, Mistry P: Guidance on the use of miglustat for treating patients with type 1 Gaucher disease. Am J Hematol. 2005, 80 (3): 223-229. 10.1002/ajh.20504
Pastores GM, Barnett NL, Kolodny EH: An open-label, noncomparative study of miglustat in type I Gaucher disease: Efficacy and tolerability over 24 months of treatment. Clin Ther. 2005, 27 (8): 1215-1227. 10.1016/j.clinthera.2005.08.004
Elstein D, Hollak C, Aerts JM, van Weely S, Maas M, Cox TM, Lachmann RH, Hrebicek M, Platt FM, Butters TD, Dwek RA, Zimran A: Sustained therapeutic effects of oral miglustat (Zavesca, N-butyldeoxynojirimycin, OGT 918) in type I Gaucher disease. J Inherit Metab Dis. 2004, 27 (6): 757-766. 10.1023/B:BOLI.0000045756.54006.17
Jeyakumar M, Norflus F, Tifft CJ, Cortina-Borja M, Butters TD, Proia RL, Perry VH, Dwek RA, Platt FM: Enhanced survival in Sandhoff disease mice receiving a combination of substrate deprivation therapy and bone marrow transplantation. Blood. 2001, 97 (1): 327-329. 10.1182/blood.V97.1.327
Jeyakumar M, Butters TD, Cortina-Borja M, Hunnam V, Proia RL, Perry VH, Dwek RA, Platt FM: Delayed symptom onset and increased life expectancy in Sandhoff disease mice treated with N-butyldeoxynojirimycin. Proc Natl Acad Sci U S A. 1999, 96 (11): 6388-6393. 10.1073/pnas.96.11.6388
Platt FM, Neises GR, Reinkensmeier G, Townsend MJ, Perry VH, Proia RL, Winchester B, Dwek RA, Butters TD: Prevention of lysosomal storage in Tay-Sachs mice treated with N-butyldeoxynojirimycin. Science. 1997, 276 (5311): 428-431. 10.1126/science.276.5311.428
Wenger DA, Suzuki K, Suzuki Y, Suzuki K: Galactosylceramide Lipidosis: Globoid Cell Leukodystrophy (Krabbe disease). The metabolic and molecular bases of inherited disease. Edited by: Scriver CR BALSWSVD. 2001, 3: 3669-3694. New York , McGraw-Hill Professional Publishing, 8th
Kobayashi T, Yamanaka T, Jacobs JM, Teixeira F, Suzuki K, Duchen LW, Eicher EM, Scaravilli F: The Twitcher mouse: an enzymatically authentic model of human globoid cell leukodystrophy (Krabbe disease). Brain Res. 1980, 202 (2): 479-483. 10.1016/0006-8993(80)90159-6
Duchen LW, Eicher EM, Jacobs JM, Scaravilli F, Teixeira F: Hereditary leucodystrophy in the mouse: the new mutant twitcher. Brain. 1980, 103 (3): 695-710.
Ezoe T, Vanier MT, Oya Y, Popko B, Tohyama J, Matsuda J, Suzuki K: Twitcher mice with only a single active galactosylceramide synthase gene exhibit clearly detectable but therapeutically minor phenotypic improvements. J Neurosci Res. 2000, 59 (2): 179-187. 10.1002/(SICI)1097-4547(20000115)59:2<179::AID-JNR4>3.0.CO;2-N
Svennerholm L, Fredman P: A procedure for the quantitative isolation of brain gangliosides. Biochim Biophys Acta. 1980, 617 (1): 97-109.
Svennerholm L, Fredman P, Jungbjer B, Mansson JE, Rynmark BM, Bostrom K, Hagberg B, Noren L, Santavuori P: Large alterations in ganglioside and neutral glycosphingolipid patterns in brains from cases with infantile neuronal ceroid lipofuscinosis/polyunsaturated fatty acid lipidosis. J Neurochem. 1987, 49 (6): 1772-1783.
Baird IL, Winborn WB, Bockman DE: A technique of decalcification suited to electron microscopy of tissues closely associated with bone. Anat Rec. 1967, 159 (3): 281-289. 10.1002/ar.1091590306
Schott I, Hartmann D, Gieselmann V, Lullmann-Rauch R: Sulfatide storage in visceral organs of arylsulfatase A-deficient mice. Virchows Arch. 2001, 439 (1): 90-96. 10.1007/s004280000360
Financial support was obtained from the German Research Foundation, Flemish Ministry of Education, Born-Bunge Foundation and Belgian Foundation of Scientific Research FWO.
The author(s) declare that they have no competing interests.
SF was responsible for the mating of mice, designed the study, organized the collaboration and finalized the manuscript. DW and RLR carried out the histological experiment and participated in the design of the manuscript. JEM carried out the lipid analysis of brain samples. RD'H and PPDD performed the behavioral testings of the animals. UM and VG participated in the design and coordination of the study and helped to draft the manuscript. All authors read and approved the final manuscript.
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Franken, S., Wittke, D., Mansson, J. et al. Modest phenotypic improvements in ASA-deficient mice with only one UDP-galactose:ceramide-galactosyltransferase gene. Lipids Health Dis 5, 21 (2006). https://doi.org/10.1186/1476-511X-5-21
- Enzyme Replacement Therapy
- Fabry Disease
- Gauche Disease
- Spiral Ganglion