Altered glycosylation of α-dystroglycan in neurons of Fukuyama congenital muscular dystrophy brains

Brain Research

Volumn 1075, Issue 1, 2006, Pages 223-228

  Saito, Yoshiaki ^a,b   Yamamoto, Tomoko ^a   Mizuguchi, Masashi ^c   Kobayashi, Makio ^a   Saito, Kayoko ^a   Ohno, Kousaku ^b   Osawa, Makiko ^a  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^b TOTTORI UNIVERSITY   (Japan)

^c UNIVERSITY OF TOKYO   (Japan)

Author keywords

Dystroglycan; Fukutin; Fukuyama congenital muscular dystrophy; Glia limitans; Glycosylation

Indexed keywords

ALPHA DYSTROGLYCAN; EPITOPE; FUKUTIN; POLYSACCHARIDE;

ADOLESCENT; ANTIBODY LABELING; ARTICLE; BLOOD VESSEL WALL; BRAIN NERVE CELL; BRAIN REGION; CLINICAL ARTICLE; CONTROLLED STUDY; FRAGMENTATION REACTION; FUKUYAMA CONGENITAL MUSCULAR DYSTROPHY; GLIA CELL; GLYCOSYLATION; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; IMMUNOREACTIVITY; MICROGYRIA; PRIORITY JOURNAL;

ADOLESCENT; ADULT; DYSTROGLYCANS; FEMALE; GLYCOSYLATION; HIPPOCAMPUS; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MUSCULAR DYSTROPHIES; NEUROGLIA; NEURONS; REFERENCE VALUES;

EID: 33644893128     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2005.12.108     Document Type: Article

References (30)

1. L. Aravind, and E.V. Koonin The fukutin protein family-predicted enzymes modifying cell-surface molecules Curr. Biol. 9 1999 R836 R837
2. K.P. Campbell, and S.D. Kahl Association of dystrophin and an integral membrane protein Nature 338 1989 259 262
3. D.B.-V. De Bernabé, S. Currier, A. Steinbrecher, J. Celli, E. van Beusekom, B. van der Zwaag, H. Kayserili, L. Merlini, D. Chitayat, W.B. Dobyns, B. Cormand, A.-E. Lehesjoki, J. Cruces, T. Voit, C.A. Walsh, H. van Bokhoven, and H.G. Brunner Mutations in the O-mannosyltransferase gene POMT1 give rise to the severe neuronal migration disorder Walker-Warburg syndrome Am. J. Hum. Genet. 71 2002 1033 1043
4. J.M. Ervasti, and K.P. Campbell A role for the dystrophin-glycoprotein complex as a transmembrane linker between laminin and actin J. Cell Biol. 122 1993 809 823
5. J.M. Ervasti, K. Ohlendieck, S.D. Kahl, M.G. Gaver, and K.P. Campbell Deficiency of a glycoprotein component of the dystrophin complex in dystrophic muscle Nature 345 1990 315 319
6. S.H. Gee, R.W. Blacher, P.J. Douville, P.R. Provost, P.D. Yurchenco, and S. Carbonetto Laminin-binding protein 120 from brain is closely related to the dystrophin-associated glycoprotein, dystroglycan, and binds with high affinity to the major heparin binding domain of laminin J. Biol. Chem. 268 1993 14972 14980
7. D.C. Górecki, J.M.J. Derry, and E.A. Barnard Dystroglycan: brain localization and chromosome mapping in the mouse Hum. Mol. Genet. 3 1994 1589 1597
8. P.K. Grewal, P.J. Holzfeind, R. Bittner, and J.E. Hewitt Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse Nat. Genet. 28 2001 151 154
9. P.K. Grewal, J.M. McLaughlan, J.C. Moore, C.A. Browning, and J.E. Hewitt Characterization of the LARGE family of putative glycosyltransferases associated with dystroglycanopathies Glycobiology 15 2005 (Jun 15) 912 923
10. Y.K. Hayashi, M. Ogawa, K. Tagawa, S. Noguchi, T. Ishihara, I. Nonaka, and K. Arahata Selective deficiency of α-dystroglycan in Fukuyama-type congenital muscular dystrophy Neurology 57 2001 115 121
11. M.D. Henry, and K.P. Campbell Dystroglycan inside and out Curr. Opin. Cell Biol. 11 1999 602 607
12. R. Herrmann, V. Straub, M. Blank, C. Kutzick, N. Franke, E.N. Jacob, H.G. Lenard, S. Kröger, and T. Voit Dissociation of the dystroglycan complex in caveolin-3-deficient limb girdle muscular dystrophy Hum. Mol. Genet. 9 2000 2335 2340
13. O. Ibraghimov-Beskrovnaya, J.M. Ervasti, J. Leveille, C.A. Slaughter, S.W. Sernett, and K.P. Campbell Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix Nature 355 1992 696 702
14. S. Kamoshita, Y. Konishi, M. Segawa, and Y. Fukuyama Congenital muscular dystrophy as a disease of the central nervous system Arch. Neurol. 33 1976 513 516
15. I. Knuesel, R.A. Zuellig, M.C. Schaub, and J.-M. Fritschy Alterations in dystrophin and utrophin expression parallel the reorganization of GABAergic synapses in a mouse model of temporal lobe epilepsy Eur. J. Neurosci. 13 2001 1113 1124
16. K. Kobayashi, Y. Nakahori, M. Miyake, K. Matsumura, E. Kondo-Iida, Y. Nomura, M. Segawa, M. Yoshioka, K. Saito, M. Osawa, K. Hamano, Y. Sakakihara, I. Nonaka, Y. Nakagome, I. Kanazawa, Y. Nakamura, K. Tokunaga, and T. Toda An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy Nature 394 1998 388 392
17. S. Levi, R.M. Grady, M.D. Henry, K.P. Campbell, J.R. Sanes, and A.M. Craig Dystroglycan is selectively associated with inhibitory GABAergic synapses but is dispensable for their differentiation J. Neurosci. 22 2002 4274 4285
18. H.G.W. Litov, T.J. Byers, S.C. Watkins, and L.M. Kunkel Localization of dystrophin to postsynaptic regions of central nervous system cortical neurons Nature 348 1990 725 728
19. D.E. Michele, and K.P. Campbell Dystrophin-glycoprotein complex: post-translational processing and dystroglycan function J. Biol. Chem. 278 2003 15457 15460
20. D.E. Michele, R. Barresi, M. Kanagawa, F. Saito, R.D. Cohn, J.S. Satz, J. Dollar, I. Nishino, R.I. Kelley, H. Somer, V. Straub, K.D. Mathews, S.A. Moore, and K.P. Campbell Post-transcriptional disruption of dystroglycan-ligand interactions in congenital muscular dystrophies Nature 418 2002 417 422
21. S.A. Moore, F. Saito, J. Chen, D.E. Michele, M.D. Henry, A. Messing, R.D. Cohn, S.E. Ross-Barta, S. Westra, R.A. Williamson, T. Hoshi, and K.P. Campbell Deletion of brain dystroglycan recapitulates aspects of congenital muscular dystrophy Nature 418 2002 422 425
22. I. Nakano, M. Funahashi, K. Takada, and T. Toda Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? Pathological study of the cerebral cortex of an FCMD fetus Acta Neuropathol. 91 1996 313 321
23. E. Ohtsuka-Tsurumi, Y. Saito, T. Yamamoto, T. Voit, M. Kobayashi, and M. Osawa Co-localization of fukutin and alpha-dystroglycan in the mouse central nervous system Brain Res. Dev. Brain Res. 152 2004 121 127
24. Q. Qu, and F.I. Smith Alpha-dystroglycan interactions affect cerebellar granule neuron migration J. Neurosci. Res. 76 2004 771 782
25. Y. Saito, M. Mizuguchi, A. Oka, and S. Takashima Fukutiin protein is expressed in neurons of the normal developing human brain but is reduced in Fukuyama-type congenital muscular dystrophy brain Ann. Neurol. 47 2000 756 764
26. J. Sasaki, K. Ishikawa, K. Kobayashi, E. Kondo-Iida, M. Fukayama, H. Mizusawa, S. Takashima, Y. Sakakihara, Y. Nakamura, and T. Toda Neuronal expression of the fukutin gene Hum. Mol. Genet. 9 2000 3083 3090
27. K. Takada, H. Nakamura, K. Suzumori, T. Ishikawa, and N. Sugiyama Cortical dysplasia in a 23-week fetus with Fukuyama congenital muscular dystrophy (FCMD) Acta Neuropathol. 74 1987 300 306
28. T. Yamamoto, Y. Kato, M. Karita, H. Takeiri, F. Muramatsu, M. Kobayashi, K. Saito, and M. Osawa Fukutin expression in glial cells and neurons: implication in the brain lesions of Fukuyama congenital muscular dystrophy Acta Neuropathol. 104 2002 217 224
29. A. Yoshida, K. Kobayashi, H. Manya, K. Taniguchi, H. Kano, M. Mizuno, T. Inazu, H. Mitsuhashi, S. Takahashi, M. Takeuchi, R. Herrmann, V. Straub, B. Talim, T. Voit, H. Topaloglu, T. Toda, and T. Endo Muscular dystrophy and neuronal migration disorder caused by mutations in a glycosyltransferase, POMGnT1 Dev. Cell 1 2001 717 724
30. M.L. Zaccaria, F. Di Tommaso, A. Brancaccio, P. Paggi, and T.C. Petrucci Dystroglycan distribution in adult mouse brain: a light and electron microscopy study Neuroscience 104 2001 311 324