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通过浦肯野细胞特异性消融cGMP依赖性蛋白激酶I对长时程抑制和小脑学习的损害。

Impairment of LTD and cerebellar learning by Purkinje cell-specific ablation of cGMP-dependent protein kinase I.

作者信息

Feil Robert, Hartmann Jana, Luo Chongde, Wolfsgruber Wiebke, Schilling Karl, Feil Susanne, Barski Jaroslaw J, Meyer Michael, Konnerth Arthur, De Zeeuw Chris I, Hofmann Franz

机构信息

Institut für Pharmakologie und Toxikologie, Technische Universität, Biedersteiner Str. 29, D-80802 München, Germany.

出版信息

J Cell Biol. 2003 Oct 27;163(2):295-302. doi: 10.1083/jcb.200306148. Epub 2003 Oct 20.

Abstract

The molecular basis for cerebellar plasticity and motor learning remains controversial. Cerebellar Purkinje cells (PCs) contain a high concentration of cGMP-dependent protein kinase type I (cGKI). To investigate the function of cGKI in long-term depression (LTD) and cerebellar learning, we have generated conditional knockout mice lacking cGKI selectively in PCs. These cGKI mutants had a normal cerebellar morphology and intact synaptic calcium signaling, but strongly reduced LTD. Interestingly, no defects in general behavior and motor performance could be detected in the LTD-deficient mice, but the mutants exhibited an impaired adaptation of the vestibulo-ocular reflex (VOR). These results indicate that cGKI in PCs is dispensable for general motor coordination, but that it is required for cerebellar LTD and specific forms of motor learning, namely the adaptation of the VOR.

摘要

小脑可塑性和运动学习的分子基础仍存在争议。小脑浦肯野细胞(PCs)含有高浓度的I型环磷酸鸟苷依赖性蛋白激酶(cGKI)。为了研究cGKI在长时程抑制(LTD)和小脑学习中的功能,我们构建了在PCs中选择性缺失cGKI的条件性敲除小鼠。这些cGKI突变体具有正常的小脑形态和完整的突触钙信号,但LTD明显减弱。有趣的是,在LTD缺陷小鼠中未检测到一般行为和运动表现的缺陷,但突变体表现出前庭眼反射(VOR)适应性受损。这些结果表明,PCs中的cGKI对于一般运动协调并非必需,但对于小脑LTD和特定形式的运动学习,即VOR的适应性是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aa4a/2173527/0169d1f25f02/200306148f1.jpg

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