A preliminary study of solid embryonic cerebellar graft survival in adult B6CBA Lurcher mutant and wild type mice
Language English Country United States Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
19943350
DOI
10.1002/ar.20967
Knihovny.cz E-resources
- MeSH
- Cell Differentiation physiology MeSH
- Disease Models, Animal MeSH
- Cerebellum cytology embryology transplantation MeSH
- Mice, Neurologic Mutants MeSH
- Mice MeSH
- Cerebellar Diseases genetics physiopathology surgery MeSH
- Neurodegenerative Diseases genetics physiopathology surgery MeSH
- Neurogenesis physiology MeSH
- Pilot Projects MeSH
- Cell Movement physiology MeSH
- Graft Survival physiology MeSH
- Nerve Regeneration physiology MeSH
- Growth Cones physiology ultrastructure MeSH
- Brain Tissue Transplantation methods MeSH
- Treatment Outcome MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Lurcher mutant mice represent a model of olivocerebellar degeneration. They suffer from complete loss of Purkinje cells and a reduction of granule cells and inferior olive neurons. Their wild type littermates serve as healthy controls. The aim of the work was to compare solid embryonic cerebellar graft survival within a period of 9 weeks after their transplantation in adult Lurcher mutant and wild type mice of the B6CBA strain. The solid grafts were injected through a hole in the occipital bone. Host mice were sacrificed 3, 6, or 9 weeks after the transplantation and their cerebella and brain-stems were examined histologically to assess graft presence and structure. We did not find significant differences in graft survival rates between Lurcher mutant and wild type mice. The frequency of graft presence did not differ between mice examined 3, 6, and 9 weeks after the transplantation, neither in Lurchers nor in wild type mice. The grafts were of various sizes. In some cases, only small residua of the grafts were found. Nerve fiber sprouting and cell migration from the graft to the host tissue were observed more often in wild type mice than in Lurchers when examined 6 weeks after surgery. In the period 3-9 weeks after transplantation, massive dying out of the grafts was not observed despite regressive processes in some of the grafts. The degenerative changes in the Lurcher mutant cerebellum do not have strong impact on the fate of the solid cerebellar graft.
References provided by Crossref.org
Lurcher Mouse as a Model of Cerebellar Syndromes
Quantification of Solid Embryonic Cerebellar Graft Volume in a Degenerative Ataxia Model
Embryonic Cerebellar Graft Morphology Differs in Two Mouse Models of Cerebellar Degeneration
Long-Term Development of Embryonic Cerebellar Grafts in Two Strains of Lurcher Mice
Experimental neurotransplantation treatment for hereditary cerebellar ataxias
Transplantation of Embryonic Cerebellar Grafts Improves Gait Parameters in Ataxic Lurcher Mice