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病毒介导的基因转移至海马CA1区可恢复脑源性神经营养因子突变小鼠的长时程增强效应。

Virus-mediated gene transfer into hippocampal CA1 region restores long-term potentiation in brain-derived neurotrophic factor mutant mice.

作者信息

Korte M, Griesbeck O, Gravel C, Carroll P, Staiger V, Thoenen H, Bonhoeffer T

机构信息

Max-Planck-Institut für Psychiatrie, München-Martinsried, Germany.

出版信息

Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12547-52. doi: 10.1073/pnas.93.22.12547.

Abstract

Long-term potentiation (LTP) has been shown to be impaired in mice deficient in the brain-derived neurotrophic factor (BDNF) gene, as well as in a number of other knockout animals. Despite its power the gene-targeting approach is always fraught with the danger of looking at the cumulative direct and indirect effects of the absence of a particular gene rather than its immediate function. The re-expression of a specific gene at a selective time point and at a specific site in gene-defective mutants presents a potent procedure to overcome this limitation and to evaluate the causal relationship between the absence of a particular gene and the impairment of a function in gene-defective animals. Here we demonstrate that the re-expression of the BDNF gene in the CA1 region almost completely restores the severely impaired LTP in hippocampal slices of BDNF-deficient mice. The results therefore provide strong evidence for the direct involvement of BDNF in the process of LTP.

摘要

长期增强效应(LTP)在脑源性神经营养因子(BDNF)基因缺陷的小鼠以及其他一些基因敲除动物中已被证明受到损害。尽管基因靶向方法很强大,但它总是充满风险,可能观察到的是特定基因缺失的累积直接和间接效应,而非其直接功能。在基因缺陷突变体的选择性时间点和特定位点重新表达特定基因,是克服这一局限性并评估特定基因缺失与基因缺陷动物功能受损之间因果关系的有效方法。在此,我们证明在CA1区域重新表达BDNF基因几乎能完全恢复BDNF缺陷小鼠海马切片中严重受损的LTP。因此,这些结果为BDNF直接参与LTP过程提供了有力证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63e5/38029/34434e101472/pnas01526-0506-a.jpg

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