Long-Term Development of Embryonic Cerebellar Grafts in Two Strains of Lurcher Mice
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články
Grantová podpora
716217
Grantová Agentura, Univerzita Karlova
National Sustainability Program I (NPU I) Nr. LO1503
Ministry of Education Youth and Sports of the Czech Republic
Q39
Univerzita Karlova v Praze
260 394
Univerzita Karlova v Praze
PubMed
29450804
DOI
10.1007/s12311-018-0928-3
PII: 10.1007/s12311-018-0928-3
Knihovny.cz E-zdroje
- Klíčová slova
- Cerebellar degeneration, Cerebellum, Lurcher mouse, Purkinje cell, Transplantation,
- MeSH
- druhová specificita MeSH
- longitudinální studie MeSH
- metoda rotující tyčky MeSH
- modely nemocí na zvířatech MeSH
- motorické dovednosti MeSH
- mozeček embryologie patologie transplantace MeSH
- myši - mutanty neurologické MeSH
- myši inbrední C3H MeSH
- myši inbrední CBA MeSH
- myši transgenní MeSH
- nemoci mozečku patologie patofyziologie terapie MeSH
- neurodegenerativní nemoci patologie patofyziologie terapie MeSH
- přežívání štěpu * fyziologie MeSH
- transplantace mozkové tkáně * MeSH
- zelené fluorescenční proteiny genetika metabolismus MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- enhanced green fluorescent protein MeSH Prohlížeč
- zelené fluorescenční proteiny MeSH
For many degenerative cerebellar diseases, currently, no effective treatment that would substantially restore cerebellar functions is available. Neurotransplantation could be a promising therapy for such cases. Nevertheless, there are still severe limitations for routine clinical use. The aim of the work was to assess volume and morphology and functional impact on motor skills of an embryonic cerebellar graft injected in the form of cell suspension in Lurcher mutant and wild-type mice of the B6CBA and C3H strains after a 6-month survival period. The grafts survived in the majority of the mice. In both B6CBA and C3H Lurcher mice, most of the grafts were strictly delimited with no tendency to invade the host cerebellum, while in wild-type mice, graft-derived Purkinje cells colonized the host's cerebellum. In C3H Lurcher mice, but not in B6CBA Lurchers, the grafts had smaller volume than in their wild-type counterparts. C3H wild-type mice had significantly larger grafts than B6CBA wild-type mice. No positive effect of the transplantation on performance in the rotarod test was observed. The findings suggest that the niche of the Lurcher mutant cerebellum has a negative impact on integration of grafted cells. This factor seems to be limiting for specific functional effects of the transplantation therapy in this mouse model of cerebellar degeneration.
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