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      <dc:title>Long-time effects of an experimental therapy with mesenchymal stem cells in congenital hydrocephalus</dc:title>
      <dc:creator>García-Bonilla, María</dc:creator>
      <dc:creator>Ojeda-Pérez, Betsaida</dc:creator>
      <dc:creator>Shumilov, Kirill</dc:creator>
      <dc:creator>Vitorica Ferrández, Javier</dc:creator>
      <dc:creator>Guitérrez, Antonia</dc:creator>
      <dc:creator>Páez-González, Patricia</dc:creator>
      <dc:creator>Jiménez-Lara, Antonio Jesús</dc:creator>
      <dc:subject>Hidrocefalia</dc:subject>
      <dc:subject>Espina bífida</dc:subject>
      <dc:description>Introduction:&#xd;
Bone marrow-derived mesenchymal stem cells (BM-MSC) are a potential therapeutic tool due to their ability for migrating and producing neuroprotector factors when they are transplanted in other neurodegenerative diseases. Moreover, some investigations have shown that BM-MSC are able to modulate astrocyte activation and neuroprotector factor production. The aim of this study was to evaluate the long-time effects of a BM-MSC experimental therapy in the hyh mouse model of congenital hydrocephalus.&#xd;
&#xd;
Methods:&#xd;
BM-MSC were characterized in vitro and then transplanted into the ventricles of young hydrocephalic hyh mice, before they develop the severe hydrocephalus. Non-hydrocephalic normal mice (wt) and hydrocephalic hyh mice sham-injected (sterile saline serum) were used as controls. Samples were studied by analyzing and comparing mRNA, protein level expressions and immunoreaction related with the progression and severity of hydrocephalus.&#xd;
&#xd;
Results:&#xd;
Fourteen days after transplantation, hydrocephalic hyh mice with BM-MSC showed lower ventriculomegaly. In these animals, BM-MSC were found undifferentiated and spread into the periventricular astrocyte reaction. There, BM-MSC were detected producing several neuroprotector factors (BDNF, GDNF, NGF, VEGF), in the same way as reactive astrocytes. Total neocortical levels of NGF, TGF-β and VEGF were found increased in hydrocephalic hyh mice transplanted with BM-MSC. Furthermore, astrocytes showed increased expressions of aquaporin-4 (water channel protein) and Slit-2 (neuroprotective and anti-inflammatory molecule).&#xd;
&#xd;
Conclusions:&#xd;
BM-MSC seem to lead to recovery of the severe neurodegenerative conditions associated to congenital hydrocephalus mediated by reactive astrocytes.</dc:description>
      <dc:date>2019-07-03T10:15:13Z</dc:date>
      <dc:date>2019-07-03T10:15:13Z</dc:date>
      <dc:date>2019</dc:date>
      <dc:date>2019-07-03</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>https://hdl.handle.net/10630/17934</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>63rd Annual Meeting of the Society for Research into Spina Bifida and Hydrocephalus</dc:relation>
      <dc:relation>La Laguna, Tenerife, Spain</dc:relation>
      <dc:relation>25/5/2019</dc:relation>
      <dc:rights>open access</dc:rights>
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