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青少年特发性脊柱侧凸:脊柱弯曲的离奇故事。

Adolescent Idiopathic Scoliosis: Fishy Tales of Crooked Spines.

机构信息

Institute of Molecular and Cell Biology, Proteos, 61 Biopolis Drive, 138673, Singapore; Department of Biological Sciences, National University of Singapore, 14 Science Drive 4, 117543, Singapore; Department of Pediatrics, Yong Loo Lin School of Medicine, National University of Singapore, 1E Kent Ridge Road, 119288, Singapore.

出版信息

Trends Genet. 2021 Jul;37(7):612-615. doi: 10.1016/j.tig.2021.03.004. Epub 2021 Apr 12.

DOI:10.1016/j.tig.2021.03.004
PMID:33858671
Abstract

Adolescent idiopathic scoliosis (AIS) is a common skeletal disorder, characterized by abnormal spine curvatures. In zebrafish, cilia-driven cerebrospinal fluid flow and urotensin II pathway activity are required for proper spine morphogenesis. Genetic studies with AIS patients now establish a conservation of the zebrafish findings in the etiology of the disease.

摘要

青少年特发性脊柱侧凸(AIS)是一种常见的骨骼疾病,其特征是脊柱异常弯曲。在斑马鱼中,纤毛驱动的脑脊液流动和尾加压素 II 通路活性对于正常的脊柱形态发生是必需的。对 AIS 患者的遗传研究现在确立了斑马鱼研究结果在疾病病因学中的保守性。

相似文献

1
Adolescent Idiopathic Scoliosis: Fishy Tales of Crooked Spines.青少年特发性脊柱侧凸:脊柱弯曲的离奇故事。
Trends Genet. 2021 Jul;37(7):612-615. doi: 10.1016/j.tig.2021.03.004. Epub 2021 Apr 12.
2
On being the right shape: Roles for motile cilia and cerebrospinal fluid flow in body and spine morphology.关于正确形态:运动性纤毛和脑脊液流动在身体及脊柱形态形成中的作用。
Semin Cell Dev Biol. 2021 Feb;110:104-112. doi: 10.1016/j.semcdb.2020.07.005. Epub 2020 Jul 18.
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Cilia-driven cerebrospinal fluid flow directs expression of urotensin neuropeptides to straighten the vertebrate body axis.纤毛驱动的脑脊液流动指导尿鸟素神经肽的表达,使脊椎动物体轴变直。
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Reissner fibre-induced urotensin signalling from cerebrospinal fluid-contacting neurons prevents scoliosis of the vertebrate spine.脑脊膜接触神经元中的 Reissner 纤维诱导的尾加压素信号防止脊椎动物脊柱侧凸。
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Urotensin II-related peptides, Urp1 and Urp2, control zebrafish spine morphology.Urotensin II 相关肽,Urp1 和 Urp2,控制斑马鱼脊柱形态。
Elife. 2022 Dec 1;11:e83883. doi: 10.7554/eLife.83883.
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The axonemal dynein heavy chain 10 gene is essential for monocilia motility and spine alignment in zebrafish.轴丝动力蛋白重链 10 基因对于斑马鱼的纤毛运动和脊柱排列至关重要。
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Zebrafish models of idiopathic scoliosis link cerebrospinal fluid flow defects to spine curvature.特发性脊柱侧凸的斑马鱼模型将脑脊液流动缺陷与脊柱弯曲联系起来。
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SCO-Spondin Defects and Neuroinflammation Are Conserved Mechanisms Driving Spinal Deformity across Genetic Models of Idiopathic Scoliosis.SCO-Spondin 缺陷和神经炎症是导致特发性脊柱侧凸遗传模型脊柱畸形的保守机制。
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Novel Mutations in UTS2R are Associated with Adolescent Idiopathic Scoliosis in the Chinese Population.UTS2R 中的新突变与中国青少年特发性脊柱侧凸有关。
Spine (Phila Pa 1976). 2021 Mar 1;46(5):E288-E293. doi: 10.1097/BRS.0000000000003786.

引用本文的文献

1
The role of cilia during organogenesis in zebrafish.斑马鱼器官发生过程中纤毛的作用。
Open Biol. 2023 Dec;13(12):230228. doi: 10.1098/rsob.230228. Epub 2023 Dec 13.
2
Urotensin II-related peptides, Urp1 and Urp2, control zebrafish spine morphology.Urotensin II 相关肽,Urp1 和 Urp2,控制斑马鱼脊柱形态。
Elife. 2022 Dec 1;11:e83883. doi: 10.7554/eLife.83883.
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Hnrnpul1 controls transcription, splicing, and modulates skeletal and limb development in vivo.Hnrnpul1 控制转录、剪接,并在体内调节骨骼和肢体发育。
G3 (Bethesda). 2022 May 6;12(5). doi: 10.1093/g3journal/jkac067.
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Conserved role of the urotensin II receptor 4 signalling pathway to control body straightness in a tetrapod.保守的尾加压素 II 受体 4 信号通路在四足动物控制身体挺直中的作用。
Open Biol. 2021 Aug;11(8):210065. doi: 10.1098/rsob.210065. Epub 2021 Aug 11.