La maladie de Parkinson en France (serveur d'exploration)

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Caspase-3: A vulnerability factor and final effector in apoptotic death of dopaminergic neurons in Parkinson's disease

Identifieur interne : 000212 ( Pmc/Curation ); précédent : 000211; suivant : 000213

Caspase-3: A vulnerability factor and final effector in apoptotic death of dopaminergic neurons in Parkinson's disease

Auteurs : Andreas Hartmann [France] ; Stéphane Hunot [France] ; Patrick P. Michel [France] ; Marie-Paule Muriel [France] ; Sheela Vyas [Royaume-Uni] ; Baptiste A. Faucheux [France] ; Annick Mouatt-Prigent [France] ; Hélène Turmel [France] ; Anu Srinivasan [États-Unis] ; Merle Ruberg [France] ; Gerard I. Evan [Royaume-Uni] ; Yves Agid [France] ; Etienne C. Hirsch [France]

Source :

RBID : PMC:16023

Abstract

Caspase-3 is an effector of apoptosis in experimental models of Parkinson's disease (PD). However, its potential role in the human pathology remains to be demonstrated. Using caspase-3 immunohistochemistry on the postmortem human brain, we observed a positive correlation between the degree of neuronal loss in dopaminergic (DA) cell groups affected in the mesencephalon of PD patients and the percentage of caspase-3-positive neurons in these cell groups in control subjects and a significant decrease of caspase-3-positive pigmented neurons in the substantia nigra pars compacta of PD patients compared with controls that also could be observed in an animal model of PD. This suggests that neurons expressing caspase-3 are more sensitive to the pathological process than those that do not express the protein. In addition, using an antibody raised against activated caspase-3, the percentage of active caspase-3-positive neurons among DA neurons was significantly higher in PD patients than in controls. Finally, electron microscopy analysis in the human brain and in vitro data suggest that caspase-3 activation precedes and is not a consequence of apoptotic cell death in PD.


Url:
PubMed: 10688892
PubMed Central: 16023

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PMC:16023

Le document en format XML

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<p>Caspase-3 is an effector of apoptosis in experimental models of Parkinson's disease (PD). However, its potential role in the human pathology remains to be demonstrated. Using caspase-3 immunohistochemistry on the postmortem human brain, we observed a positive correlation between the degree of neuronal loss in dopaminergic (DA) cell groups affected in the mesencephalon of PD patients and the percentage of caspase-3-positive neurons in these cell groups in control subjects and a significant decrease of caspase-3-positive pigmented neurons in the substantia nigra pars compacta of PD patients compared with controls that also could be observed in an animal model of PD. This suggests that neurons expressing caspase-3 are more sensitive to the pathological process than those that do not express the protein. In addition, using an antibody raised against activated caspase-3, the percentage of active caspase-3-positive neurons among DA neurons was significantly higher in PD patients than in controls. Finally, electron microscopy analysis in the human brain and
<italic>in vitro</italic>
data suggest that caspase-3 activation precedes and is not a consequence of apoptotic cell death in PD.</p>
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<name>
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<given-names>Andreas</given-names>
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<name>
<surname>Hunot</surname>
<given-names>Stéphane</given-names>
</name>
<xref ref-type="aff" rid="N0x9ea9268.0xa03f080">*</xref>
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<name>
<surname>Michel</surname>
<given-names>Patrick P.</given-names>
</name>
<xref ref-type="aff" rid="N0x9ea9268.0xa03f080">*</xref>
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<contrib contrib-type="author">
<name>
<surname>Muriel</surname>
<given-names>Marie-Paule</given-names>
</name>
<xref ref-type="aff" rid="N0x9ea9268.0xa03f080">*</xref>
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<name>
<surname>Vyas</surname>
<given-names>Sheela</given-names>
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<surname>Faucheux</surname>
<given-names>Baptiste A.</given-names>
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<xref ref-type="aff" rid="N0x9ea9268.0xa03f080">*</xref>
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<name>
<surname>Mouatt-Prigent</surname>
<given-names>Annick</given-names>
</name>
<xref ref-type="aff" rid="N0x9ea9268.0xa03f080">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Turmel</surname>
<given-names>Hélène</given-names>
</name>
<xref ref-type="aff" rid="N0x9ea9268.0xa03f080">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Srinivasan</surname>
<given-names>Anu</given-names>
</name>
<xref ref-type="aff" rid="N0x9ea9268.0xa03f080"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ruberg</surname>
<given-names>Merle</given-names>
</name>
<xref ref-type="aff" rid="N0x9ea9268.0xa03f080">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Evan</surname>
<given-names>Gerard I.</given-names>
</name>
<xref ref-type="aff" rid="N0x9ea9268.0xa03f080"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Agid</surname>
<given-names>Yves</given-names>
</name>
<xref ref-type="aff" rid="N0x9ea9268.0xa03f080">*</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Hirsch</surname>
<given-names>Etienne C.</given-names>
</name>
<xref ref-type="aff" rid="N0x9ea9268.0xa03f080">*</xref>
<xref ref-type="author-notes" rid="FN153">§</xref>
</contrib>
</contrib-group>
<aff id="N0x9ea9268.0xa03f080">
<label>*</label>
Institut National de la Santé et de la Recherche Médicale U 289, Hôpital de la Salpêtrière, 47 Boulevard de l′Hôpital, 75013 Paris, France;
<label></label>
Imperial Cancer Research Fund Laboratories, 44 Lincoln's Inn Field, London WC2A 3PX, United Kingdom; and
<label></label>
IDUN Pharmaceuticals Inc., 11085 North Pines Road, La Jolla, CA 92037</aff>
<author-notes>
<fn id="FN153">
<label>§</label>
<p>To whom reprint requests should be addressed. E-mail:
<email>hirsch@ccr.jussieu.fr</email>
.</p>
</fn>
<fn>
<p>Communicated by Jean-Pierre Changeux, Institut Pasteur, Paris, France</p>
</fn>
</author-notes>
<pub-date pub-type="ppub">
<day>14</day>
<month>3</month>
<year>2000</year>
</pub-date>
<pub-date pub-type="epub">
<day>25</day>
<month>2</month>
<year>2000</year>
</pub-date>
<volume>97</volume>
<issue>6</issue>
<fpage>2875</fpage>
<lpage>2880</lpage>
<history>
<date date-type="received">
<day>20</day>
<month>8</month>
<year>1999</year>
</date>
<date date-type="accepted">
<day>20</day>
<month>12</month>
<year>1999</year>
</date>
</history>
<copyright-statement>Copyright © 2000, The National Academy of Sciences</copyright-statement>
<copyright-year>2000</copyright-year>
<abstract>
<p>Caspase-3 is an effector of apoptosis in experimental models of Parkinson's disease (PD). However, its potential role in the human pathology remains to be demonstrated. Using caspase-3 immunohistochemistry on the postmortem human brain, we observed a positive correlation between the degree of neuronal loss in dopaminergic (DA) cell groups affected in the mesencephalon of PD patients and the percentage of caspase-3-positive neurons in these cell groups in control subjects and a significant decrease of caspase-3-positive pigmented neurons in the substantia nigra pars compacta of PD patients compared with controls that also could be observed in an animal model of PD. This suggests that neurons expressing caspase-3 are more sensitive to the pathological process than those that do not express the protein. In addition, using an antibody raised against activated caspase-3, the percentage of active caspase-3-positive neurons among DA neurons was significantly higher in PD patients than in controls. Finally, electron microscopy analysis in the human brain and
<italic>in vitro</italic>
data suggest that caspase-3 activation precedes and is not a consequence of apoptotic cell death in PD.</p>
</abstract>
</article-meta>
</front>
</pmc>
</record>

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