Viscogliosi Laboratory in Molecular Genetics of Musculoskeletal Diseases, Sainte-Justine University Hospital Research Center, Montreal, Quebec, H3T 1C5, Canada.
Department of Biochemistry and Molecular Medicine, Faculty of Medicine, Université de Montreal, Montreal, Quebec, H3T 1J4, Canada.
Sci Rep. 2017 Mar 14;7:44260. doi: 10.1038/srep44260.
The primary cilium is an outward projecting antenna-like organelle with an important role in bone mechanotransduction. The capacity to sense mechanical stimuli can affect important cellular and molecular aspects of bone tissue. Idiopathic scoliosis (IS) is a complex pediatric disease of unknown cause, defined by abnormal spinal curvatures. We demonstrate significant elongation of primary cilia in IS patient bone cells. In response to mechanical stimulation, these IS cells differentially express osteogenic factors, mechanosensitive genes, and signaling genes. Considering that numerous ciliary genes are associated with a scoliosis phenotype, among ciliopathies and knockout animal models, we expected IS patients to have an accumulation of rare variants in ciliary genes. Instead, our SKAT-O analysis of whole exomes showed an enrichment among IS patients for rare variants in genes with a role in cellular mechanotransduction. Our data indicates defective cilia in IS bone cells, which may be linked to heterogeneous gene variants pertaining to cellular mechanotransduction.
初级纤毛是一种向外突出的天线状细胞器,在骨骼机械转导中具有重要作用。感知机械刺激的能力会影响骨组织的重要细胞和分子方面。特发性脊柱侧凸(IS)是一种病因不明的复杂儿科疾病,其特征是脊柱异常弯曲。我们在 IS 患者的骨细胞中观察到初级纤毛显著伸长。这些 IS 细胞对机械刺激表现出不同的成骨因子、机械敏感基因和信号基因表达。考虑到众多纤毛基因与脊柱侧凸表型相关,包括纤毛病和敲除动物模型,我们预计 IS 患者在纤毛基因中会积累罕见变异。相反,我们对整个外显子组的 SKAT-O 分析显示,IS 患者中与细胞机械转导相关的基因中的罕见变异富集。我们的数据表明 IS 骨细胞中的纤毛缺陷,这可能与细胞机械转导相关的异质基因变异有关。