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一种用于追踪黑质纹状体多巴胺能神经元轴突生长的小鼠模型。

A mouse model for tracking nigrostriatal dopamine neuron axon growth.

作者信息

Vives Joaquim, Sasajala Piriya, Chang Kuo Hsuan, Zhao Suling, Li Meng

机构信息

Institute for Stem Cell Research, University of Edinburgh, Edinburgh EH9 3JQ, United Kingdom.

出版信息

Genesis. 2008 Mar;46(3):125-31. doi: 10.1002/dvg.20375.

Abstract

The midbrain dopaminergic system, which consists of neurons of the substantia nigra and the ventral tegmental area, is a subject of intense interest, since the loss of neurons from the substantia nigra results in motor disorders characteristic of Parkinson's disease. We have generated a knock-in reporter mouse line with the tau-lacZ fusion gene inserted into the Pitx3 locus via homologous recombination. This approach permitted the visualisation of midbrain specific dopaminergic axonal tracts from both the substantia nigra and the ventral tegmental area in phenotypically normal heterozygous Pitx3-taulacZ brain tissues, either in situ or following culture in vitro, by a simple and sensitive beta-galactosidase enzyme reaction. Thus the Pitx3-taulacZ mice could serve as a valuable tool for the identification of molecules regulating midbrain dopaminergic neuritogenesis, either in vivo in combination with genetic manipulation in mice, or in vitro using organ cultures.

摘要

中脑多巴胺能系统由黑质和腹侧被盖区的神经元组成,由于黑质神经元的丧失会导致帕金森病的特征性运动障碍,因此该系统备受关注。我们通过同源重组,将tau-lacZ融合基因插入Pitx3基因座,构建了一种敲入报告基因小鼠品系。这种方法可以通过简单且灵敏的β-半乳糖苷酶反应,在表型正常的杂合Pitx3-taulacZ脑组织中,原位或体外培养后,观察到来自黑质和腹侧被盖区的中脑特异性多巴胺能轴突束。因此,Pitx3-taulacZ小鼠可作为一种有价值的工具,用于在体内结合小鼠基因操作或在体外使用器官培养来鉴定调节中脑多巴胺能神经突发生的分子。

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