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Expression of tyrosine hydroxylase in cerebellar Purkinje neurons of the mutant tottering and leaner mouse.

作者信息

Austin M C, Schultzberg M, Abbott L C, Montpied P, Evers J R, Paul S M, Crawley J N

机构信息

Unit on Behavioral Neuropharmarcology, National Institute of Mental Health, Bethesda, MD 20892.

出版信息

Brain Res Mol Brain Res. 1992 Oct;15(3-4):227-40. doi: 10.1016/0169-328x(92)90113-p.

DOI:10.1016/0169-328x(92)90113-p
PMID:1279353
Abstract

In situ hybridization histochemistry, Northern blot analysis and immunohistochemistry were used to examine tyrosine hydroxylase (TH) mRNA concentrations and immunoreactivity in the locus coeruleus and cerebellum of the tottering (tg/tg), leaner (tgla/tgla), compound heterozygous (tg/tgla) and wild type control (+/+) mice, bred on a C57BL/6J background. Cerebellar Purkinje neurons, long considered to be GABAergic, showed high levels of TH mRNA in the caudal vermis and the lateral hemispheres of the cerebellum of tg/tg, tg/tgla, and tgla/tgla mice. Analysis of grain density over individual Purkinje cells showed significantly greater concentrations of TH mRNA in tg/tg, tg/tgla, and tgla/tgla mice as compared to +/+ wild type control mice. Comparison of adult (greater than or equal to 2 months) and young, pre-seizure (less than or equal to 3 weeks) mutant mice showed Purkinje cells densely labelled for TH mRNA at both ages, suggesting that TH gene expression in Purkinje cells is independent of the onset of seizures. Northern blot analysis confirmed the findings from the in situ hybridization studies, demonstrating a single band identical to TH mRNA. Immunohistochemistry confirmed the presence of TH protein in Purkinje cells of the caudal vermis and the lateral hemispheres of the cerebellum in both control and mutant mice. Quantitation of mRNA for TH and the coexisting neuropeptide, galanin, in the locus coeruleus detected no significant differences between adult tg/tg, tg/tgla and +/+ control mice. The present findings demonstrate that the classically GABAergic Purkinje cells in the cerebellum express low levels of TH, and that the mutant tottering and leaner strains of mice express extremely high levels of mRNA and protein for TH.

摘要

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1
Expression of tyrosine hydroxylase in cerebellar Purkinje neurons of the mutant tottering and leaner mouse.
Brain Res Mol Brain Res. 1992 Oct;15(3-4):227-40. doi: 10.1016/0169-328x(92)90113-p.
2
Regulation of tyrosine hydroxylase expression in tottering mouse Purkinje cells.蹒跚小鼠浦肯野细胞中酪氨酸羟化酶表达的调控
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Co-localization of tyrosine hydroxylase and zebrin II immunoreactivities in Purkinje cells of the mutant mice, tottering and tottering/leaner.酪氨酸羟化酶与zebrin II免疫反应性在突变小鼠(蹒跚和蹒跚/瘦型)浦肯野细胞中的共定位。
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Tottering and leaner mutations perturb transient developmental expression of tyrosine hydroxylase in embryologically distinct Purkinje cells.
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Single tottering mutations responsible for the neuropathic phenotype of the P-type calcium channel.导致P型钙通道神经病变表型的单个蹒跚突变。
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Fluoro-jade identification of cerebellar granule cell and purkinje cell death in the alpha1A calcium ion channel mutant mouse, leaner.利用荧光玉鉴定α1A钙离子通道突变小鼠(瘦素小鼠)小脑颗粒细胞和浦肯野细胞的死亡情况。
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