Li Chun, Ma Yu, Zhang Kunshan, Gu Junjie, Tang Fan, Chen Shengdi, Cao Li, Li Siguang, Jin Ying
Laboratory of Molecular Developmental Biology, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.
Stem Cell Translational Research Center, Tongji Hospital, Tongji University School of Medicine, Shanghai 200065, China.
Oncotarget. 2016 Aug 16;7(33):53611-53627. doi: 10.18632/oncotarget.10680.
Paroxysmal kinesigenic dyskinesia (PKD) is an episodic movement disorder with autosomal-dominant inheritance and marked variability in clinical manifestations.Proline-rich transmembrane protein 2 (PRRT2) has been identified as a causative gene of PKD, but the molecular mechanism underlying the pathogenesis of PKD still remains a mystery. The phenotypes and transcriptional patterns of the PKD disease need further clarification. Here, we report the generation and neural differentiation of iPSC lines from two familial PKD patients with c.487C>T (p. Gln163X) and c.573dupT (p. Gly192Trpfs*8) PRRT2 mutations, respectively. Notably, an extremely lower efficiency in neural conversion from PKD-iPSCs than control-iPSCs is observed by a step-wise neural differentiation method of dual inhibition of SMAD signaling. Moreover, we show the high expression level of PRRT2 throughout the human brain and the expression pattern of PRRT2 in other human tissues for the first time. To gain molecular insight into the development of the disease, we conduct global gene expression profiling of PKD cells at four different stages of neural induction and identify altered gene expression patterns, which peculiarly reflect dysregulated neural transcriptome signatures and a differentiation tendency to mesodermal development, in comparison to control-iPSCs. Additionally, functional and signaling pathway analyses indicate significantly different cell fate determination between PKD-iPSCs and control-iPSCs. Together, the establishment of PKD-specific in vitro models and the illustration of transcriptome features in PKD cells would certainly help us with better understanding of the defects in neural conversion as well as further investigations in the pathogenesis of the PKD disease.
发作性运动诱发性运动障碍(PKD)是一种具有常染色体显性遗传且临床表现显著变异的发作性运动障碍。富含脯氨酸的跨膜蛋白2(PRRT2)已被确定为PKD的致病基因,但PKD发病机制的分子机制仍不清楚。PKD疾病的表型和转录模式需要进一步阐明。在此,我们报告了分别从两名患有c.487C>T(p.Gln163X)和c.573dupT(p.Gly192Trpfs*8)PRRT2突变的家族性PKD患者中诱导多能干细胞(iPSC)系的生成及其神经分化。值得注意的是,通过双抑制SMAD信号的逐步神经分化方法,观察到PKD-iPSC向神经细胞转化的效率比对照iPSC极低。此外,我们首次展示了PRRT2在整个人脑中的高表达水平以及PRRT2在其他人体组织中的表达模式。为了深入了解该疾病的发展机制,我们对神经诱导四个不同阶段的PKD细胞进行了全基因组表达谱分析,并确定了基因表达模式的改变,与对照iPSC相比,这些改变特别反映了神经转录组特征失调以及向中胚层发育的分化趋势。此外,功能和信号通路分析表明PKD-iPSC和对照iPSC之间细胞命运决定存在显著差异。总之,PKD特异性体外模型的建立以及PKD细胞转录组特征的阐述肯定有助于我们更好地理解神经转化中的缺陷以及对PKD疾病发病机制的进一步研究。