Spiró Zoltán, Koh Angela, Tay Shermaine, See Kelvin, Winkler Christoph
Department of Biological Sciences, National University of Singapore, Singapore.
NUS Centre for BioImaging Sciences (CBIS), Singapore.
Sci Rep. 2016 Jun 7;6:27470. doi: 10.1038/srep27470.
An unresolved mystery in the field of spinal muscular atrophy (SMA) is why a reduction of the ubiquitously expressed Smn protein causes defects mostly in motoneurons. We addressed the possibility that this restricted vulnerability stems from elevated Smn expression in motoneurons. To explore this, we established an ex vivo zebrafish culture system of GFP-marked motoneurons to quantitatively measure Smn protein and smn mRNA levels as well as promoter activity in motoneurons versus other cell types. Importantly, we uncovered that Smn levels are elevated in motoneurons by means of transcriptional activation. In addition, we identified the ETS family transcription factor Etv5b to be responsible for increased smn transcription in motoneurons. Moreover, we established that the additional supply of Smn protein in motoneurons is necessary for proper axonogenesis in a cell-autonomous manner. These findings demonstrate the reliance of motoneurons on more Smn, thereby adding a novel piece of evidence for their increased vulnerability under SMA conditions.
脊髓性肌萎缩症(SMA)领域一个尚未解决的谜团是,为何普遍表达的生存运动神经元蛋白(Smn)减少主要会导致运动神经元出现缺陷。我们探讨了这种有限易损性源于运动神经元中Smn表达升高的可能性。为了探究这一点,我们建立了一个绿色荧光蛋白(GFP)标记的运动神经元的离体斑马鱼培养系统,以定量测量运动神经元与其他细胞类型中Smn蛋白、smn mRNA水平以及启动子活性。重要的是,我们发现通过转录激活,运动神经元中的Smn水平会升高。此外,我们确定ETS家族转录因子Etv5b是运动神经元中smn转录增加的原因。而且,我们证实运动神经元中额外补充Smn蛋白对于以细胞自主方式进行正常轴突形成是必要的。这些发现证明了运动神经元对更多Smn的依赖性,从而为它们在SMA条件下易损性增加增添了新的证据。