Movement Disorders (revue)

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Cell type‐specific neuronal loss in the putamen of patients with multiple system atrophy

Identifieur interne : 002F66 ( Main/Exploration ); précédent : 002F65; suivant : 002F67

Cell type‐specific neuronal loss in the putamen of patients with multiple system atrophy

Auteurs : Kenta Sato [Japon] ; Ryuji Kaji [Japon] ; Sadayuki Matsumoto [Japon] ; Satoshi Goto [Japon]

Source :

RBID : ISTEX:82D7E5D647067812CD396FB00B3790D3EAA69E24

Descripteurs français

English descriptors

Abstract

Using antibodies to calcineurin (CaN) and choline acetyltransferase (ChAT), we performed topographical and cellular immunohistochemical analysis on the posterior putamen of autopsied patients with multiple system atrophy with predominant parkinsonism (MSA‐P). We document that in these patients, medium spiny neurons positive for CaN were severely depleted in the dorsolateral portion of the posterior putamen where ChAT‐positive neurons are normally distributed. Our findings indicate that in patients with MSA‐P, striatal neurons manifest a cell type‐specific vulnerability to neurodegeneration. © 2007 Movement Disorder Society

Url:
DOI: 10.1002/mds.21385


Affiliations:


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Le document en format XML

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<term>Human</term>
<term>Humans</term>
<term>Immunoenzyme Techniques</term>
<term>Middle Aged</term>
<term>Multiple System Atrophy (pathology)</term>
<term>Multiple system atrophy</term>
<term>Nerve Degeneration (pathology)</term>
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<div type="abstract" xml:lang="en">Using antibodies to calcineurin (CaN) and choline acetyltransferase (ChAT), we performed topographical and cellular immunohistochemical analysis on the posterior putamen of autopsied patients with multiple system atrophy with predominant parkinsonism (MSA‐P). We document that in these patients, medium spiny neurons positive for CaN were severely depleted in the dorsolateral portion of the posterior putamen where ChAT‐positive neurons are normally distributed. Our findings indicate that in patients with MSA‐P, striatal neurons manifest a cell type‐specific vulnerability to neurodegeneration. © 2007 Movement Disorder Society</div>
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