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LBX1 表达的改变与小鼠能量代谢相关参数的变化有关。

The alteration of LBX1 expression is associated with changes in parameters related to energy metabolism in mice.

机构信息

Department of Orthopedic Surgery, National Defense Medical College, Tokorozawa, Saitama, Japan.

Division of Cardiovascular Medicine, Department of Internal Medicine I, National Defense Medical College, Tokorozawa, Saitama, Japan.

出版信息

PLoS One. 2024 Aug 7;19(8):e0308445. doi: 10.1371/journal.pone.0308445. eCollection 2024.

DOI:10.1371/journal.pone.0308445
PMID:39110747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11305531/
Abstract

The LBX1 gene is located near a single nucleotide polymorphism that is highly associated with susceptibility to adolescent idiopathic scoliosis and is considered one of the strongest candidate genes involved in the pathogenesis of this condition. We have previously found that loss of LBX1 from skeletal muscle results not only in spinal deformity but also in lean body mass, suggesting a potential role for LBX1 in energy metabolism. The purpose of the present study was to test this hypothesis by analyzing the phenotype of mice lacking LBX1 in skeletal muscle with a focus on energy metabolism. We found that loss of LBX1 rendered mice more resistant to high-fat diet-induced obesity, despite comparable food intake between mutant and control mice. Notably, the mutant mice exhibited improved glucose tolerance, increased maximal aerobic capacity, and higher core body temperature compared to control mice. In addition, we found that overexpression of LBX1 decreased glucose uptake in cultured cells. Taken together, our data show that LBX1 functions as a negative regulator of energy metabolism and that loss of LBX1 from skeletal muscle increases systemic energy expenditure resulting in lean body mass. The present study thus suggests a potential association between LBX1 dysfunction and lean body mass in patients with adolescent idiopathic scoliosis.

摘要

LBX1 基因位于一个单核苷酸多态性附近,该多态性与青少年特发性脊柱侧凸的易感性高度相关,被认为是参与该病发病机制的最强候选基因之一。我们之前发现,LBX1 从骨骼肌中的缺失不仅导致脊柱畸形,还导致瘦体重减少,这表明 LBX1 在能量代谢中可能具有潜在作用。本研究的目的是通过分析骨骼肌中缺乏 LBX1 的小鼠表型来检验这一假设,重点关注能量代谢。我们发现,尽管突变体和对照组小鼠的食物摄入量相当,但 LBX1 的缺失使小鼠对高脂肪饮食诱导的肥胖具有更强的抵抗力。值得注意的是,与对照组小鼠相比,突变体小鼠表现出更好的葡萄糖耐量、更高的最大有氧能力和更高的核心体温。此外,我们发现 LBX1 的过表达降低了培养细胞中的葡萄糖摄取。总之,我们的数据表明 LBX1 作为能量代谢的负调节剂发挥作用,而骨骼肌中 LBX1 的缺失增加了全身能量消耗,导致瘦体重减少。因此,本研究提示 LBX1 功能障碍与青少年特发性脊柱侧凸患者的瘦体重减少之间可能存在关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fb4/11305531/906dd25d5648/pone.0308445.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fb4/11305531/cd4616a5a0bb/pone.0308445.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fb4/11305531/fe4913feaaaf/pone.0308445.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fb4/11305531/c9a1aa9eaeab/pone.0308445.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fb4/11305531/906dd25d5648/pone.0308445.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fb4/11305531/cd4616a5a0bb/pone.0308445.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fb4/11305531/fe4913feaaaf/pone.0308445.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fb4/11305531/c9a1aa9eaeab/pone.0308445.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fb4/11305531/906dd25d5648/pone.0308445.g004.jpg

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本文引用的文献

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Is There a Relationship between Idiopathic Scoliosis and Body Mass? A Scoping Review.特发性脊柱侧凸与体重之间是否存在关系?系统评价。
Nutrients. 2022 Sep 27;14(19):4011. doi: 10.3390/nu14194011.
2
Abrogation of LBX1 in skeletal muscle results in hypoplastic limbs and progressive kyphosis in mice.骨骼肌中LBX1的缺失会导致小鼠肢体发育不全和进行性脊柱后凸。
J Orthop Res. 2023 Apr;41(4):884-890. doi: 10.1002/jor.25417. Epub 2022 Jul 31.
3
Biological effect of dysregulated LBX1 on adolescent idiopathic scoliosis through modulating muscle carbohydrate metabolism.
LBX1失调通过调节肌肉碳水化合物代谢对青少年特发性脊柱侧凸的生物学效应。
Spine J. 2022 Sep;22(9):1551-1565. doi: 10.1016/j.spinee.2022.04.005. Epub 2022 Apr 21.
4
Nontargeted Metabolomic Analysis of Plasma Metabolite Changes in Patients with Adolescent Idiopathic Scoliosis.青少年特发性脊柱侧凸患者血浆代谢物变化的非靶向代谢组学分析。
Mediators Inflamm. 2021 May 25;2021:5537811. doi: 10.1155/2021/5537811. eCollection 2021.
5
Body Composition in Japanese Girls with Adolescent Idiopathic Scoliosis.患有青少年特发性脊柱侧弯的日本女孩的身体成分
Spine Surg Relat Res. 2020 Aug 31;5(2):68-74. doi: 10.22603/ssrr.2020-0088. eCollection 2021.
6
The Susceptibility and Potential Functions of the LBX1 Gene in Adolescent Idiopathic Scoliosis.LBX1基因在青少年特发性脊柱侧凸中的易感性及潜在作用
Front Genet. 2021 Jan 18;11:614984. doi: 10.3389/fgene.2020.614984. eCollection 2020.
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Mss51 deletion increases endurance and ameliorates histopathology in the mdx mouse model of Duchenne muscular dystrophy.Mss51 缺失增加了 Duchenne 肌营养不良症 mdx 小鼠模型的耐力并改善了组织病理学。
FASEB J. 2021 Feb;35(2):e21276. doi: 10.1096/fj.202002106RR.
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Spine (Phila Pa 1976). 2021 Apr 1;46(7):440-446. doi: 10.1097/BRS.0000000000003885.
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