Ramos Belén, Valín Alvaro, Sun Xinxin, Gill Grace
Department of Anatomy and Cellular Biology, Tufts University School of Medicine, 136 Harrison Ave., Boston, MA 02111, USA.
Mol Cell Neurosci. 2009 Oct;42(2):152-9. doi: 10.1016/j.mcn.2009.06.008. Epub 2009 Jun 22.
Regulation of neuronal gene expression is critical to establish functional connections in the mammalian nervous system. The transcription factor Sp4 regulates dendritic patterning during cerebellar granule neuron development by limiting branching and promoting activity-dependent pruning. Here, we investigate neurotrophin-3 (NT3) as a target gene important for Sp4-dependent dendritic morphogenesis. We found that Sp4 overexpression reduced NT3 promoter activity whereas knockdown of Sp4 increased NT3 promoter activity and mRNA. Moreover, Sp4 bound to the NT3 promoter in vivo, supporting a direct role for Sp4 as a repressor of NT3 expression. Addition of exogenous NT3 promoted dendritic branching in cerebellar granule neurons. Furthermore, sequestering NT3 blocked the continued addition of dendritic branches observed upon Sp4 knockdown, but had no effect on dendrite pruning. These findings demonstrate that, during cerebellar granule neuron development, Sp4-dependent repression of neurotrophin-3 is required to limit dendritic branching and thereby promote acquisition of the mature dendritic pattern.
神经元基因表达的调控对于在哺乳动物神经系统中建立功能连接至关重要。转录因子Sp4通过限制分支并促进活动依赖性修剪,在小脑颗粒神经元发育过程中调节树突形态。在此,我们研究神经营养因子-3(NT3)作为对Sp4依赖性树突形态发生重要的靶基因。我们发现Sp4过表达降低了NT3启动子活性,而Sp4敲低则增加了NT3启动子活性和mRNA。此外,Sp4在体内与NT3启动子结合,支持Sp4作为NT3表达阻遏物的直接作用。添加外源性NT3促进了小脑颗粒神经元的树突分支。此外,隔离NT3阻断了在Sp4敲低时观察到的树突分支的持续增加,但对树突修剪没有影响。这些发现表明,在小脑颗粒神经元发育过程中,需要Sp4依赖性抑制神经营养因子-3来限制树突分支,从而促进成熟树突模式的形成。