Generation and characterization of cerebellar granule neurons specific knockout mice of Golli-MBP.
Haruko MiyazakiSaki NishiokaTomoyuki YamanakaManabu AbeYukio ImamuraTomohiro MiyasakaNobuto KakudaToshitaka OohashiTomomi ShimogoriKazuhiro YamakawaMasahito IkawaNobuyuki NukinaPublished in: Transgenic research (2024)
Golli-myelin basic proteins, encoded by the myelin basic protein gene, are widely expressed in neurons and oligodendrocytes in the central nervous system. Further, prior research has shown that Golli-myelin basic protein is necessary for myelination and neuronal maturation during central nervous system development. In this study, we established Golli-myelin basic protein-floxed mice to elucidate the cell-type-specific effects of Golli-myelin basic protein knockout through the generation of conditional knockout mice (Golli-myelin basic proteins fl/fl ; E3CreN), in which Golli-myelin basic proteins were specifically deleted in cerebellar granule neurons, where Golli-myelin basic proteins are expressed abundantly in wild-type mice. To investigate the role of Golli-myelin basic proteins in cerebellar granule neurons, we further performed histopathological analyses of these mice, with results indicating no morphological changes or degeneration of the major cellular components of the cerebellum. Furthermore, behavioral analysis showed that Golli-myelin basic proteins fl/fl ; E3CreN mice were healthy and did not display any abnormal behavior. These results suggest that the loss of Golli-myelin basic proteins in cerebellar granule neurons does not lead to cerebellar perturbations or behavioral abnormalities. This mouse model could therefore be employed to analyze the effect of Golli-myelin basic protein deletion in specific cell types of the central nervous system, such as other neuronal cells and oligodendrocytes, or in lymphocytes of the immune system.
Keyphrases
- white matter
- wild type
- spinal cord
- mouse model
- protein protein
- high fat diet induced
- multiple sclerosis
- induced apoptosis
- single cell
- dna methylation
- small molecule
- bone marrow
- genome wide
- type diabetes
- oxidative stress
- copy number
- cell proliferation
- cerebrospinal fluid
- adipose tissue
- mesenchymal stem cells
- metabolic syndrome
- brain injury
- peripheral blood
- cerebral ischemia