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通过肌节分裂实现肌肉生长。

Muscle growth by sarcomere divisions.

作者信息

Rodier Clement, Estabrook Ian D, Chan Eunice HoYee, Rice Gavin, Loreau Vincent, Raunser Stefan, Görlich Dirk, Friedrich Benjamin M, Schnorrer Frank

机构信息

CNRS, IBDM, Turing Centre for Living Systems, Aix Marseille University, Marseille, France.

Cluster of Excellence "Physics of Life," Technical University Dresden, Dresden, Germany.

出版信息

Sci Adv. 2025 Jul 11;11(28):eadw9445. doi: 10.1126/sciadv.adw9445. Epub 2025 Jul 9.

DOI:10.1126/sciadv.adw9445
PMID:40632866
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12239948/
Abstract

The sarcomere is the elementary contractile unit of muscles. Adult muscle cells are large and chain thousands of sarcomeres into long periodic myofibrils that attach to the skeleton. During development, muscle cells must increase in length to maintain the mechanical connection to the growing skeleton. How muscles add new sarcomeres to facilitate muscle growth is unknown. Using live imaging and high-throughput image analysis, we have now tracked the sarcomere components during the developmental growth of muscle and found that individual sarcomeres divide along the myofibril tension axis into daughter sarcomeres. This way, new sarcomeres can be inserted into contractile and mechanically intact myofibrils. We propose that sarcomere division is triggered by tension and local sarcomere damage originating from skeletal growth and muscle contractions. Sarcomere divisions repair damaged sarcomeres, ensure their mechanical integrity, and synchronize sarcomere addition with skeletal growth during animal development.

摘要

肌节是肌肉的基本收缩单位。成年肌肉细胞很大,将数千个肌节连成附着在骨骼上的长周期肌原纤维。在发育过程中,肌肉细胞必须增长长度以维持与生长中的骨骼的机械连接。肌肉如何添加新的肌节以促进肌肉生长尚不清楚。利用实时成像和高通量图像分析,我们现在追踪了肌肉发育生长过程中的肌节成分,发现单个肌节沿肌原纤维张力轴分裂为子肌节。通过这种方式,新的肌节可以插入到收缩性和机械完整性良好的肌原纤维中。我们提出,肌节分裂是由骨骼生长和肌肉收缩引起的张力和局部肌节损伤触发的。肌节分裂修复受损的肌节,确保其机械完整性,并在动物发育过程中使肌节添加与骨骼生长同步。

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Sci Adv. 2025 May 9;11(19):eads8716. doi: 10.1126/sciadv.ads8716.
2
Structure of the native myosin filament in the relaxed cardiac sarcomere.心肌节段弛豫时天然肌球蛋白丝的结构。
Nature. 2023 Nov;623(7988):863-871. doi: 10.1038/s41586-023-06690-5. Epub 2023 Nov 1.
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UCSF ChimeraX: Tools for structure building and analysis.UCSF ChimeraX:结构构建和分析工具。
Protein Sci. 2023 Nov;32(11):e4792. doi: 10.1002/pro.4792.
4
Nanobodies combined with DNA-PAINT super-resolution reveal a staggered titin nanoarchitecture in flight muscles.纳米抗体与 DNA-PAINT 超分辨率技术结合揭示了飞行肌中交错的肌联蛋白纳米结构。
Elife. 2023 Jan 16;12:e79344. doi: 10.7554/eLife.79344.
5
A nanobody toolbox to investigate localisation and dynamics of titins and other key sarcomeric proteins.纳米体工具包可用于研究原肌球蛋白和其他关键肌节蛋白的定位和动态。
Elife. 2023 Jan 16;12:e79343. doi: 10.7554/eLife.79343.
6
Tension-driven multi-scale self-organisation in human iPSC-derived muscle fibers.人诱导多能干细胞源性肌纤维中的张力驱动多尺度自组织。
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Mechanobiology of muscle and myofibril morphogenesis.肌肉与肌原纤维形态发生的机械生物学
Cells Dev. 2021 Dec;168:203760. doi: 10.1016/j.cdev.2021.203760. Epub 2021 Dec 1.
8
Myofibril and mitochondria morphogenesis are coordinated by a mechanical feedback mechanism in muscle.肌原纤维和线粒体形态发生受肌肉内机械反馈机制的协调。
Nat Commun. 2021 Apr 7;12(1):2091. doi: 10.1038/s41467-021-22058-7.
9
The Hippo pathway controls myofibril assembly and muscle fiber growth by regulating sarcomeric gene expression.Hippo 通路通过调节肌节基因表达控制肌原纤维组装和肌肉纤维生长。
Elife. 2021 Jan 6;10:e63726. doi: 10.7554/eLife.63726.
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Graded titin cleavage progressively reduces tension and uncovers the source of A-band stability in contracting muscle.肌联蛋白的分级切割逐渐降低张力,并揭示收缩肌肉中A带稳定性的来源。
Elife. 2020 Dec 24;9:e64107. doi: 10.7554/eLife.64107.