Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Figures Only
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sasaki, S.
Right arrow Articles by Iwata, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sasaki, S.
Right arrow Articles by Iwata, M.
Related Collections
Right arrow Parkinson's disease/Parkinsonism
Right arrow Dementia with Lewy bodies
Right arrow All Genetics
NEUROLOGY 2004;63:678-682
© 2004 American Academy of Neurology

Parkin-positive autosomal recessive juvenile parkinsonism with {alpha}-synuclein-positive inclusions

Shoichi Sasaki, MD, Akiko Shirata, MD, Kiyomi Yamane, MD and Makoto Iwata, MD

From the Department of Neurology (Drs. Sasaki and Iwata), Neurological Institute, Tokyo Women’s Medical University, Tokyo; and Department of Neurology (Drs. Shirata and Yamane), Neurological Institute, Ohta-Atami Hospital, Koriyama, Japan.

Address correspondence to Dr. Shoichi Sasaki, Department of Neurology, Neurologic Institute, Tokyo Women’s Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan; e-mail: ssasaki{at}nij.twmu.ac.jp

Objective: To report an autopsy case of an autosomal recessive juvenile parkinsonism patient with a homozygous exon 3 deletion in the parkin gene and {alpha}-synuclein-positive inclusions.

Methods: The representative areas of the brain were embedded in paraffin, stained with hematoxylin-eosin, Klüver-Barrera, and Gallyas-Braak stainings. Immunohistochemically, some of the specimens were used for immunostaining with the antibodies to {alpha}-synuclein, ubiquitin, and phosphorylated tau (AT8). Immunoreaction was visualized by the streptavidin-biotin-peroxidase complex method.

Results: Histologically, the lesions of the brain were limited to the dopaminergic neuron system such as the substantia nigra (SN) and locus ceruleus. Melanin-containing neurons in the pars compacta of the SN were moderately to severely depleted, accompanied by gliosis. In the locus ceruleus, neurons were mildly decreased and extraneuronal melanin pigments were seen. Lewy bodies were not observed in the neuropils of the pars compacta of the SN or locus ceruleus. However, basophilic inclusion bodies were only occasionally observed in the neuropils of the pedunculopontine nucleus in the mesencephalic reticular formation. Immunohistochemistry with antibodies to {alpha}-synuclein and ubiquitin showed {alpha}-synuclein- and ubiquitin-positive inclusions in the neuropils of the pedunculopontine nucleus, which had a doughnut or round shape.

Conclusions: A variety of parkin gene abnormalities may produce pathologic differences in the degree and distribution of neuronal degeneration, including the absence or presence of Lewy bodies. A relationship between parkin-induced parkinsonism and idiopathic Parkinson disease (PD) may exist.


Received February 16, 2004. Accepted in final form April 30, 2004.




This article has been cited by other articles:


Home page
NeurologyHome page
T. Baumer, P. P. Pramstaller, H. R. Siebner, S. Schippling, J. Hagenah, M. Peller, C. Gerloff, C. Klein, and A. Munchau
Sensorimotor integration is abnormal in asymptomatic Parkin mutation carriers: A TMS study
Neurology, November 20, 2007; 69(21): 1976 - 1981.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
W. Mandemakers, V. A. Morais, and B. De Strooper
A cell biological perspective on mitochondrial dysfunction in Parkinson disease and other neurodegenerative diseases
J. Cell Sci., May 15, 2007; 120(10): 1707 - 1716.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
C. Hampe, H. Ardila-Osorio, M. Fournier, A. Brice, and O. Corti
Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin-protein ligase with monoubiquitylation capacity
Hum. Mol. Genet., July 1, 2006; 15(13): 2059 - 2075.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
L. Chen, B. Cagniard, T. Mathews, S. Jones, H. C. Koh, Y. Ding, P. M. Carvey, Z. Ling, U. J. Kang, and X. Zhuang
Age-dependent Motor Deficits and Dopaminergic Dysfunction in DJ-1 Null Mice
J. Biol. Chem., June 3, 2005; 280(22): 21418 - 21426.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Copyright © 2004 by AAN Enterprises, Inc.