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甘氨酸神经递质传递障碍导致青少年特发性脊柱侧凸。

Impaired glycine neurotransmission causes adolescent idiopathic scoliosis.

机构信息

Department of Orthopaedics and Traumatology, School of Clinical Medicine, Li Ka Shing Faculty of Medicine, University of Hong Kong, Pokfulam, Hong Kong, China.

School of Biomedical Sciences, Faculty of Medicine, Chinese University of Hong Kong, Shatin, Hong Kong, China.

出版信息

J Clin Invest. 2024 Jan 16;134(2):e168783. doi: 10.1172/JCI168783.

Abstract

Adolescent idiopathic scoliosis (AIS) is the most common form of spinal deformity, affecting millions of adolescents worldwide, but it lacks a defined theory of etiopathogenesis. Because of this, treatment of AIS is limited to bracing and/or invasive surgery after onset. Preonset diagnosis or preventive treatment remains unavailable. Here, we performed a genetic analysis of a large multicenter AIS cohort and identified disease-causing and predisposing variants of SLC6A9 in multigeneration families, trios, and sporadic patients. Variants of SLC6A9, which encodes glycine transporter 1 (GLYT1), reduced glycine-uptake activity in cells, leading to increased extracellular glycine levels and aberrant glycinergic neurotransmission. Slc6a9 mutant zebrafish exhibited discoordination of spinal neural activities and pronounced lateral spinal curvature, a phenotype resembling human patients. The penetrance and severity of curvature were sensitive to the dosage of functional glyt1. Administration of a glycine receptor antagonist or a clinically used glycine neutralizer (sodium benzoate) partially rescued the phenotype. Our results indicate a neuropathic origin for "idiopathic" scoliosis, involving the dysfunction of synaptic neurotransmission and central pattern generators (CPGs), potentially a common cause of AIS. Our work further suggests avenues for early diagnosis and intervention of AIS in preadolescents.

摘要

青少年特发性脊柱侧凸(AIS)是最常见的脊柱畸形形式,影响着全球数以百万计的青少年,但它缺乏明确的病因发病理论。正因为如此,AIS 的治疗仅限于发病后的支具和/或侵入性手术。发病前的诊断或预防性治疗仍然无法实现。在这里,我们对一个大型多中心 AIS 队列进行了遗传分析,在多代家族、三联体和散发病例中鉴定出 SLC6A9 的致病和易感变体。编码甘氨酸转运体 1(GLYT1)的 SLC6A9 变体降低了细胞中的甘氨酸摄取活性,导致细胞外甘氨酸水平升高和异常的甘氨酸能神经传递。Slc6a9 突变的斑马鱼表现出脊柱神经活动的不协调和明显的侧向脊柱弯曲,这一表型类似于人类患者。曲率的外显率和严重程度对功能性 glyt1 的剂量敏感。甘氨酸受体拮抗剂或临床使用的甘氨酸中和剂(苯甲酸钠)的给药部分挽救了表型。我们的结果表明,“特发性”脊柱侧凸的神经病变起源,涉及突触神经传递和中枢模式发生器(CPG)的功能障碍,这可能是 AIS 的共同原因。我们的工作进一步为青少年特发性脊柱侧凸的早期诊断和干预提供了途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38e3/10786698/3bdfc433d31f/jci-134-168783-g182.jpg

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