Institute of Molecular and Cell Biology, Proteos, 61 Biopolis Drive, Singapore 138673.
Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, Singapore 117543.
Biol Open. 2020 May 14;9(5):bio052027. doi: 10.1242/bio.052027.
Reissner fibre (RF), discovered by the 19-century German anatomist Ernst Reissner, is a filamentous structure present in cerebrospinal fluid (CSF). RF forms by aggregation of a glycoprotein called SCO-spondin (Sspo), but its function has remained enigmatic. Recent studies have shown that zebrafish mutants develop a curved embryonic body axis. Zebrafish embryos with impaired cilia motility also develop curved bodies, which arises from failure of expression of () genes in CSF-contacting neurons (CSF-cNs), impairing downstream signalling in trunk muscles. Here, we show that mutants can survive into adulthood, but display severe curvatures of the vertebral column, resembling the common human spine disorder idiopathic scoliosis (IS). mutants also exhibit significant reduction of gene expression from CSF-cNs. Consistent with epinephrine in CSF being bound by RF and required for expression, treating mutants with this catecholamine rescued expression of the genes and axial defects. More strikingly, providing Urp2, specifically in the CSF-cNs, rescued body curvature of homozygotes during larval stages as well as in the adult. These findings bridge existing gaps in our knowledge between cilia motility, RF, Urp signalling and spine deformities, and suggest that targeting the Urotensin pathway could provide novel therapeutic avenues for IS.
赖斯纳纤维(RF)由 19 世纪德国解剖学家恩斯特·赖斯纳(Ernst Reissner)发现,是一种存在于脑脊液(CSF)中的丝状结构。RF 是由一种叫做 SCO-粘蛋白(Sspo)的糖蛋白聚集形成的,但它的功能仍然是个谜。最近的研究表明,斑马鱼突变体发育出弯曲的胚胎体轴。纤毛运动受损的斑马鱼胚胎也会发育出弯曲的身体,这是由于 CSF 接触神经元(CSF-cNs)中 ()基因表达失败,从而破坏了躯干肌肉中的下游信号转导。在这里,我们表明 突变体可以存活到成年,但显示出严重的脊柱弯曲,类似于常见的人类脊柱疾病特发性脊柱侧凸(IS)。 突变体也表现出 CSF-cNs 中 基因表达的显著减少。与 CSF 中的肾上腺素被 RF 结合并需要用于 表达一致,用这种儿茶酚胺处理 突变体可挽救 基因的表达和轴突缺陷。更引人注目的是,在 CSF-cNs 中特异性提供 Urp2 可挽救 纯合子幼虫期以及成年期的身体弯曲。这些发现弥合了我们在纤毛运动、RF、Urp 信号和脊柱畸形之间的现有知识差距,并表明靶向 Urotensin 途径可能为 IS 提供新的治疗途径。