Characterization of spheroids in hereditary diffuse leukoencephalopathy with axonal spheroids

Journal of the Neurological Sciences

Volumn 352, Issue 1-2, 2015, Pages 74-78

  Jin, Chenghua ^a   Washimi, Yukihiko ^a   Yoshida, Kunihiro ^b   Hashizume, Yoshio ^c   Yazawa, Ikuru ^a  

^a NATIONAL CENTER FOR GERIATRICS AND GERONTOLOGY   (Japan)

^b SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c Fukushimura Hospital   (Japan)

Author keywords

Colony stimulating factor 1 receptor; Hereditary diffuse leukoencephalopathy with axonal spheroids; Neurodegeneration; Spheroids; White matter degeneration; Synuclein

Indexed keywords

ALPHA SYNUCLEIN; COLONY STIMULATING FACTOR RECEPTOR;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; AUTOPSY; AXONAL SPHEROID; BRAIN ATROPHY; BRAIN REGION; BRAIN TISSUE; CASE REPORT; COGNITION; COGNITIVE DEFECT; DEGENERATIVE DISEASE; DEMENTIA; DNA SEQUENCE; GAIT DISORDER; GENETIC VARIABILITY; HEREDITARY DIFFUSE LEUKOENCEPHALOPATHY WITH AXONAL SPHEROID; HETEROZYGOTE; HUMAN; HUMAN TISSUE; IMMUNOHISTOCHEMISTRY; INVESTIGATIVE PROCEDURES; LEUKOENCEPHALOPATHY; MALE; MIDDLE AGED; MOTOR DYSFUNCTION; NERVE DEGENERATION; NEUROIMAGING; NUCLEAR MAGNETIC RESONANCE IMAGING; PARKINSONISM; PRIORITY JOURNAL; PYRAMIDAL SIGN; FEMALE; GENETICS; NERVE FIBER; PATHOLOGY; WHITE MATTER;

ADULT; ALPHA-SYNUCLEIN; AXONS; FEMALE; HUMANS; LEUKOENCEPHALOPATHIES; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; NEURODEGENERATIVE DISEASES; RECEPTOR, MACROPHAGE COLONY-STIMULATING FACTOR; WHITE MATTER;

EID: 84928368965     PISSN: 0022510X     EISSN: 18785883     Source Type: Journal    
DOI: 10.1016/j.jns.2015.03.033     Document Type: Article

References (20)

1. B. Alberts, A. Johnson, J. Lewis, M. Raff, K. Roberts, and P. Walter Cytoskeleton Molecular Biology of the Cell 5th ed. Cytoskeleton 2008 Garland Science New York 965 1052
2. R. Axelsson, M. Röyttä, P. Sourander, H.O. Akesson, and O. Andersen Hereditary diffuse leucoencephalopathy with spheroids Acta Psychiatr Scand Suppl 314 1984 1 65
3. Y. Baba, B. Ghetti, M.C. Baker, R.J. Uitti, M.L. Hutton, and K. Yamaguchi et al. Hereditary diffuse leukoencephalopathy with spheroids: clinical, pathologic and genetic studies of a new kindred Acta Neuropathol (Berl) 111 2006 300 311
4. J. Cervós-Navarro, and H. Urich Degenerative diseases of the cerebral cortex and the white matter Metabolic and degenerative diseases of the central nervous system: pathology, biochemistry, and genetics 1995 Academic Press San Diego 497 519
5. S.H. Freeman, B.T. Hyman, K.B. Sims, E.T. Hedley-Whyte, A. Vossough, and M.P. Frosch et al. Adult onset leukodystrophy with neuroaxonal spheroids: clinical, neuroimaging and neuropathologic observations Brain Pathol 19 2009 39 47
6. K. Itoh, K. Shiga, K. Shimizu, M. Muranishi, M. Nakagawa, and S. Fushiki Autosomal dominant leukodystrophy with axonal spheroids and pigmented glia: clinical and neuropathological characteristics Acta Neuropathol (Berl) 111 2006 39 45
7. J.D. Marotti, S. Tobias, J.D. Fratkin, J.M. Powers, and C.H. Rhodes Adult onset leukodystrophy with neuroaxonal spheroids and pigmented glia: report of a family, historical perspective, and review of the literature Acta Neuropathol (Berl) 107 2004 481 488
8. S. Mizushima, and T. Nakazawa Clinical, pathological and neurochemical studies of a case of sudanophilic leukodystrophy Psychiatr Neurol Jpn 73 1971 840 853 (906-7, in Japanese with English abstract)
9. K. Nakayama, Y. Suzuki, and I. Yazawa Microtubule depolymerization suppresses α-synuclein accumulation in a mouse model of multiple system atrophy Am J Pathol 174 2009 1471 1480
10. R. Rademakers, M. Baker, A.M. Nicholson, N.J. Rutherford, N. Finch, and A. Soto-Ortolaza et al. Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids Nat Genet 44 2011 200 205
11. F. Seitelberger Neuropathological conditions related to neuroaxonal dystrophy Acta Neuropathol (Berl) suppl V 1971 17 29
12. C. Sundal, J. Lash, J. Aasly, S. Øygarden, S. Roeber, and H. Kretzschman et al. Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): a misdiagnosed disease entity J Neurol Sci 314 2012 130 137
13. Y. Suzuki, C. Jin, T. Iwase, and I. Yazawa β-III Tubulin fragments inhibit α-synuclein accumulation in models of multiple system atrophy J Biol Chem 289 2014 24374 24382
14. Y. Suzuki, C. Jin, and I. Yazawa Cystatin C triggers neuronal degeneration in a model of multiple system atrophy Am J Pathol 184 2014 790 799
15. S. Terada, H. Ishizu, O. Yokota, T. Ishihara, H. Nakashima, and A. Kugo et al. An autopsy case of hereditary diffuse leukoencephalopathy with spheroids, clinically suspected of Alzheimer's disease Acta Neuropathol (Berl) 108 2004 538 545
16. M.S. Van der Knaap, S. Naidu, B.K. Kleinschmidt-Demasters, W. Kamphorst, and H.C. Weinstein Autosomal dominant diffuse leukoencephalopathy with neuroaxonal spheroids Neurology 54 2000 463 468
17. I. Watanabe, and J. Muller Cavitating "diffuse sclerosis" J Neuropathol Exp Neurol 26 1967 437 455
18. C. Wider, J.A. Van Gerpen, S. DeArmond, E.A. Shuster, D.W. Dickson, and Z.K. Wszolek Leukoencephalopathy with spheroids (HDLS) and pigmentary leukodystrophy (POLD): a single entity? Neurology 72 2009 1953 1959
19. I. Yazawa, I. Nakano, H. Yamada, and M. Oda Long tract degeneration in familial sudanophilic leukodystrophy with prominent spheroids J Neurol Sci 147 1997 185 191
20. I. Yazawa, B.I. Giasson, R. Sasaki, B. Zhang, S. Joyce, and K. Uryu et al. Mouse model of multiple system atrophy: α-synuclein expression in oligodendrocytes causes glial and neuronal degeneration Neuron 45 2005 847 859