Suppr超能文献

脑瘫患儿挛缩肌肉中牵张诱导卫星细胞变形。

Stretch-induced satellite cell deformation incontracturedmuscles in children with cerebral palsy.

机构信息

Department of Bioengineering, University of California, San Diego, CA, USA; Department of Orthopaedic Surgery, University of California, San Diego, CA, USA.

Department of Orthopaedic Surgery, University of California, San Diego, CA, USA; Department of Veterans Affairs Medical Center, San Diego, CA, USA; Shirley Ryan AbilityLab, Chicago, IL, USA.

出版信息

J Biomech. 2021 Sep 20;126:110635. doi: 10.1016/j.jbiomech.2021.110635. Epub 2021 Jul 14.

Abstract

Satellite cells (SCs) are quiescent, adult skeletal muscle stem cells responsible for postnatal muscle growth and repair. Children with cerebral palsy (CP) have muscle contractures with reduced SC abundance, extracellular matrix abnormalities and reduced serial sarcomere number resulting in greatly increased in vivo sarcomere length, perhaps due to impaired sarcomere addition, compared to children with typical development (TD). Stretch is a strong activator of SCs that leads to addition of sarcomeres during bone-muscle growth. Mechanical loading and subsequent deformation of intracellular structures can lead to activation and proliferation, perhaps by cytoskeletal transmissions of extracellular mechanical signals to the nuclei. The primary aim of this study was to determine the effect of ex vivo stretch-induced sarcomere length change on SC deformation in children with CP and TD. Muscle biopsies were obtained from twelve children (7 CP, 5 TD) during surgery. Fiber bundles were labeled with fluorescent antibodies for Pax7 (SC), DRAQ5 (nuclei), and alpha-actinin (sarcomere protein). Fibers were stretched using a custom jig and imaged using confocal microscopy. SC nuclear length, height and aspect ratio underwent increased deformation with increasing sarcomere length (p < 0.05) in both groups. Slopes of association for SC nuclear length, aspect ratio and sarcomere lengths were similar between CP and TD. Our results indicate that SC in children with CP undergo similar deformation as TD across sarcomere lengths.

摘要

卫星细胞(SCs)是处于静止状态的成体骨骼肌干细胞,负责出生后的肌肉生长和修复。脑瘫(CP)患儿的肌肉存在挛缩,SCs 数量减少,细胞外基质异常,串联肌节数量减少,导致体内肌节长度大大增加,这可能是由于肌节的添加受损,与典型发育(TD)的儿童相比。拉伸是SCs 的强烈激活剂,可在骨骼肌肉生长过程中添加肌节。机械加载和随后的细胞内结构变形可导致激活和增殖,这可能是通过细胞外机械信号向细胞核的细胞骨架传递。本研究的主要目的是确定体外拉伸诱导的肌节长度变化对 CP 和 TD 儿童SCs 变形的影响。在手术期间,从 12 名儿童(7 名 CP,5 名 TD)中获得肌肉活检。纤维束用荧光抗体标记 Pax7(SCs)、DRAQ5(核)和肌动蛋白(肌节蛋白)。使用定制夹具拉伸纤维,并使用共聚焦显微镜对其进行成像。在两组中,随着肌节长度的增加,SCs 核长度、高度和纵横比都经历了增加的变形(p<0.05)。CP 和 TD 之间 SC 核长度、纵横比和肌节长度的关联斜率相似。我们的结果表明,CP 患儿的SCs 在肌节长度范围内经历了与 TD 相似的变形。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验