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转录因子Sp4在小脑成熟过程中调节树突形态形成。

Transcription factor Sp4 regulates dendritic patterning during cerebellar maturation.

作者信息

Ramos Belén, Gaudillière Brice, Bonni Azad, Gill Grace

机构信息

Department of Pathology, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, MA 02115, USA.

出版信息

Proc Natl Acad Sci U S A. 2007 Jun 5;104(23):9882-7. doi: 10.1073/pnas.0701946104. Epub 2007 May 29.

Abstract

Integration of inputs by a neuron depends on dendritic arborization patterns. In mammals, the genetic programs that regulate dynamic remodeling of dendrites during development and in response to activity are incompletely understood. Here we report that knockdown of the transcription factor Sp4 led to an increased number of highly branched dendrites during maturation of cerebellar granule neurons in dissociated cultures and in cerebellar cortex. Time-course analysis revealed that depletion of Sp4 led to persistent generation of dendritic branches and a failure in resorption of transient dendrites. Depolarization induced a reduction in the number of dendrites, and knockdown of Sp4 blocked depolarization-induced remodeling. Furthermore, overexpression of Sp4 wild type, but not a mutant lacking the DNA-binding domain, was sufficient to promote dendritic pruning in nondepolarizing conditions. These findings indicate that the transcription factor Sp4 controls dendritic patterning during cerebellar development by limiting branch formation and promoting activity-dependent pruning.

摘要

神经元对输入信息的整合取决于树突分支模式。在哺乳动物中,调控树突在发育过程中以及对活动作出反应时动态重塑的遗传程序尚未完全明确。在此我们报告,在解离培养的小脑颗粒神经元成熟过程以及小脑皮质中,转录因子Sp4的敲低导致高度分支的树突数量增加。时间进程分析显示,Sp4的缺失导致树突分支持续生成以及瞬时树突吸收失败。去极化诱导树突数量减少,而Sp4的敲低则阻断了去极化诱导的重塑。此外,Sp4野生型(而非缺乏DNA结合结构域的突变体)的过表达足以在非去极化条件下促进树突修剪。这些发现表明,转录因子Sp4通过限制分支形成和促进活动依赖性修剪来控制小脑发育过程中的树突模式。

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