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PMID: 1892215 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Immunohistochemical expression of P400 protein in Purkinje cells of sphingomyelinosis mouse.

Brain & development ·Vol. 13 ·No. 2 ·1991-00-00 ·Pages 110-4

Tanaka J, Miyawaki S, Maeda N, Mikoshiba K

Abstract

Immunohistochemical expression of P400 protein, a glycoprotein localized to the Purkinje cell membrane, has been studied in the cerebellum of spm mouse using anti-P400 monoclonal antibody. The initial change observed in the Purkinje cells was a swelling of the cell body with distortion of the neurites; this occurred as early as 5 weeks of age. A significant, patchy loss of Purkinje cells started at 6 weeks before cerebellar signs became manifest. With progression of the disease the dendritic processes in the molecular layer showed a marked swelling, followed by irregular arborization and finally by disintegration. A few, heterotopic Purkinje cells were found in the subcortical white matter; this was interpreted as an indication that a disturbance in neuronal migration could be superimposed on the sphingolipid metabolic disorder. Additionally, P400-immunoreactive nerve cells were occasionally encountered in areas of the deep cerebellar nuclei and in the lateral vestibular nuclei of the pontine tegmentum. The number of P400-immunoreactive Purkinje cells correlated well with the percentages of the remaining Purkinje cells during the ages of 4 to 7 wks. At the late stage of 10 to 12 weeks almost all Purkinje cells had lost their P400-immunoreactivity. It is suggested that Purkinje cells that fail to express P400 protein may undergo an immunohistochemical degeneration of the plasma membrane.

MeSH Terms
Aging/pathology Animals Calcium Channels Cell Count Cerebellum/pathology Disease Models, Animal Immunohistochemistry Inositol 1,4,5-Trisphosphate Receptors Membrane Glycoproteins/analysis Mice Mice, Neurologic Mutants Nerve Tissue Proteins/analysis Niemann-Pick Diseases/metabolism,pathology Pons/pathology Purkinje Cells/chemistry,pathology Receptors, Cytoplasmic and Nuclear
Chemicals
Calcium Channels Inositol 1,4,5-Trisphosphate Receptors Itpr1 protein, mouse Membrane Glycoproteins Nerve Tissue Proteins Receptors, Cytoplasmic and Nuclear
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Tanaka J
Division of Neuropathology, Jikei University School of Medicine, Tokyo, Japan.
Miyawaki S
Maeda N
Mikoshiba K
Article Info
Journal
Brain & development
Abbr.
Brain Dev
ISSN
0387-7604
Published
1991-00-00
Pages
110-4
Language
English
Region
Netherlands
NLM ID
7909235
Subset
IM
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