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小脑浦肯野细胞中的基因靶向:最新进展

Genetic Targeting in Cerebellar Purkinje Cells: an Update.

作者信息

Sługocka Anna, Wiaderkiewicz Jan, Barski Jaroslaw J

机构信息

Center for Experimental Medicine, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.

Department of Physiology, School of Medicine in Katowice, Medical University of Silesia, Katowice, Poland.

出版信息

Cerebellum. 2017 Feb;16(1):191-202. doi: 10.1007/s12311-016-0770-4.

DOI:10.1007/s12311-016-0770-4
PMID:26969183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5243870/
Abstract

Since the last review paper published in Cerebellum in 2002 [1], there has been a substantial increase in the number of experiments utilizing transgenic manipulations in murine cerebellar Purkinje cells. Most of these approaches were made possible with the use of the Cre/loxP methodology and pcp2/L7 based Cre recombinase expressing transgenic mouse strains. This review aims to summarize all studies which used Purkinje cell specific transgenesis since the first use of mouse strain with Purkinje cell specific Cre expression in 2002.

摘要

自2002年在《小脑》杂志上发表上一篇综述论文[1]以来,利用转基因操作研究小鼠小脑浦肯野细胞的实验数量大幅增加。这些方法大多借助Cre/loxP技术以及基于pcp2/L7的表达Cre重组酶的转基因小鼠品系得以实现。本综述旨在总结自2002年首次使用具有浦肯野细胞特异性Cre表达的小鼠品系以来,所有使用浦肯野细胞特异性转基因技术的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7dc/5243870/1dee50202a7f/12311_2016_770_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7dc/5243870/7df0f1427afe/12311_2016_770_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7dc/5243870/f87c4275dada/12311_2016_770_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7dc/5243870/5d6a154f09cf/12311_2016_770_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7dc/5243870/1dee50202a7f/12311_2016_770_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7dc/5243870/7df0f1427afe/12311_2016_770_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7dc/5243870/f87c4275dada/12311_2016_770_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7dc/5243870/5d6a154f09cf/12311_2016_770_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f7dc/5243870/1dee50202a7f/12311_2016_770_Fig4_HTML.jpg

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2
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Purkinje cell ablation and Purkinje cell-specific deletion of Tsc1 in the developing cerebellum strengthen cerebellothalamic synapses.在发育中的小脑中,浦肯野细胞消融和浦肯野细胞特异性缺失Tsc1会增强小脑丘脑突触。
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本文引用的文献

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Role of Synchronous Activation of Cerebellar Purkinje Cell Ensembles in Multi-joint Movement Control.小脑浦肯野细胞群同步激活在多关节运动控制中的作用
Curr Biol. 2015 May 4;25(9):1157-65. doi: 10.1016/j.cub.2015.03.009. Epub 2015 Apr 2.
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Spatially selective holographic photoactivation and functional fluorescence imaging in freely behaving mice with a fiberscope.纤维镜实现自由活动小鼠的空间选择性全息光激活和功能荧光成像。
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Optogenetic modulation and multi-electrode analysis of cerebellar networks in vivo.
Purkinje 细胞特异性 SEL1L-hrd1 内质网相关降解缺陷导致小鼠进行性小脑共济失调。
JCI Insight. 2024 Nov 8;9(21):e174725. doi: 10.1172/jci.insight.174725.
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Cerebellar Heterogeneity and Selective vulnerability in Spinocerebellar Ataxia Type 1 (SCA1).小脑的异质性和脊髓小脑性共济失调 1 型 (SCA1) 的选择性易损性。
Neurobiol Dis. 2024 Jul;197:106530. doi: 10.1016/j.nbd.2024.106530. Epub 2024 May 14.
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BOD1 regulates the cerebellar IV/V lobe-fastigial nucleus circuit associated with motor coordination.BOD1 调节与运动协调相关的小脑 IV/V 叶-前庭神经核回路。
Signal Transduct Target Ther. 2022 Jun 1;7(1):170. doi: 10.1038/s41392-022-00989-x.
6
Cell Type-specific Knockout with -mediated Cre Recombination in the Developing Cerebellum.在发育中的小脑中通过介导的Cre重组进行细胞类型特异性基因敲除。
Exp Neurobiol. 2021 Jun 30;30(3):203-212. doi: 10.5607/en21017.
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ATR regulates neuronal activity by modulating presynaptic firing.ATR 通过调节突触前放电来调节神经元活动。
Nat Commun. 2021 Jul 1;12(1):4067. doi: 10.1038/s41467-021-24217-2.
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Region-specific preservation of Purkinje cell morphology and motor behavior in the ATXN1[82Q] mouse model of spinocerebellar ataxia 1.脊髓小脑共济失调1型的ATXN1[82Q]小鼠模型中浦肯野细胞形态和运动行为的区域特异性保存。
Brain Pathol. 2021 Sep;31(5):e12946. doi: 10.1111/bpa.12946. Epub 2021 Mar 16.
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In Search of Molecular Markers for Cerebellar Neurons.寻找小脑神经元的分子标志物。
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10
L7/Pcp-2-specific expression of Cre recombinase using knock-in approach.使用敲入方法实现Cre重组酶的L7/Pcp-2特异性表达。
Biochem Biophys Res Commun. 2005 Jun 17;331(4):1216-21. doi: 10.1016/j.bbrc.2005.04.043.