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<title>Apolipoprotein D mediates autocrine protection of astrocytes and controls their reactivity level, contributing to the functional maintenance of paraquat-challenged dopaminergic systems</title>
<creator>Bajo Grañeras, Raquel</creator>
<creator>Ganfornina Álvarez, María Dolores</creator>
<creator>Martín Tejedor, Esperanza</creator>
<creator>Sánchez Romero, Diego</creator>
<subject>Sistema nervioso central - Enfermedades</subject>
<description>Producción Científica</description>
<description>The study of glial derived factors induced by injury and&#xd;
degeneration is important to understand the nervous system&#xd;
response to deteriorating conditions. We focus on Apolipoprotein&#xd;
D (ApoD), a Lipocalin expressed by glia and&#xd;
strongly induced upon aging, injury or neurodegeneration.&#xd;
Here we study ApoD function in the brain of wild type and&#xd;
ApoD-KO mice by combining in vivo experiments with&#xd;
astrocyte cultures. Locomotor performance, dopamine concentration,&#xd;
and gene expression levels in the substantia&#xd;
nigra were assayed in mice treated with paraquat (PQ). The&#xd;
regulation of ApoD transcription, a molecular screening of&#xd;
oxidative stress (OS)-related genes, cell viability and oxidation&#xd;
status, and the effects of adding human ApoD were&#xd;
tested in astrocyte cultures. We demonstrate that (1) ApoD&#xd;
is required for an adequate locomotor performance, modifies&#xd;
the gene expression profile of PQ-challenged nigrostriatal&#xd;
system, and contributes to its functional maintenance; (2)&#xd;
ApoD expression in astrocytes is controlled by the OSresponsive&#xd;
JNK pathway; (3) ApoD contributes to an&#xd;
autocrine protecting mechanism in astrocytes, avoiding peroxidated&#xd;
lipids accumulation and altering the PQ transcriptional&#xd;
response of genes involved in ROS managing and the&#xd;
inflammatory response to OS; (4) Addition of human ApoD&#xd;
to ApoD-KO astrocytes promotes survival through a mechanism&#xd;
accompanied by protein internalization and modulation&#xd;
of astroglial reactivity. Our data support that ApoD&#xd;
contributes to the endurance of astrocytes and decreases&#xd;
their reactivity level in vitro and in vivo. ApoD function as&#xd;
a maintenance factor for astrocytes would suffice to explain&#xd;
the observed protection by ApoD of OS-vulnerable dopaminergic&#xd;
circuits in vivo.</description>
<date>2014-09-19</date>
<date>2015-09-19</date>
<date>2011</date>
<type>info:eu-repo/semantics/article</type>
<identifier>Glia, 2011, vol. 59, p. 1551-1566</identifier>
<identifier>0894-1491</identifier>
<identifier>http://uvadoc.uva.es/handle/10324/6085</identifier>
<identifier>10.1002/glia.21200</identifier>
<identifier>1551</identifier>
<identifier>1566</identifier>
<identifier>Glia</identifier>
<identifier>59</identifier>
<language>eng</language>
<rights>info:eu-repo/semantics/openAccess</rights>
<rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</rights>
<rights>Attribution-NonCommercial-NoDerivatives 4.0 International</rights>
<publisher>Wiley-Liss</publisher>
</thesis></metadata></record></GetRecord></OAI-PMH>