Actuating Extracellular Matrices Decouple the Mechanical and Biochemical Effects of Muscle Contraction on Motor Neurons.

IF 10 2区 医学 Q1 ENGINEERING, BIOMEDICAL
Angel Bu, Ferdows Afghah, Nicolas Castro, Maheera Bawa, Sonika Kohli, Karina Shah, Brandon Rios, Vincent Butty, Ritu Raman
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Abstract

Emerging in vivo evidence suggests that repeated muscle contraction, or exercise, impacts peripheral nerves. However, the difficulty of isolating the muscle-specific impact on motor neurons in vivo, as well as the inability to decouple the biochemical and mechanical impacts of muscle contraction in this setting, motivates investigating this phenomenon in vitro. This study demonstrates that tuning the mechanical properties of fibrin enables longitudinal culture of highly contractile skeletal muscle monolayers, enabling functional characterization of and long-term secretome harvesting from exercised tissues. Motor neurons stimulated with exercised muscle-secreted factors significantly upregulate neurite outgrowth and migration, with an effect size dependent on muscle contraction intensity. Actuating magnetic microparticles embedded within fibrin hydrogels enable dynamically stretching motor neurons and non-invasively mimicking the mechanical effects of muscle contraction. Interestingly, axonogenesis is similarly upregulated in both mechanically and biochemically stimulated motor neurons, but RNA sequencing reveals different transcriptomic signatures between groups, with biochemical stimulation having a greater impact on cell signaling related to axonogenesis and synapse maturation. This study leverages actuating extracellular matrices to robustly validate a previously hypothesized role for muscle contraction in regulating motor neuron growth and maturation from the bottom-up through both mechanical and biochemical signaling.

致动细胞外基质使肌肉收缩对运动神经元的机械效应和生化效应脱钩
越来越多的体内证据表明,反复的肌肉收缩或运动会影响周围神经。然而,在体内很难分离出肌肉对运动神经元的特异性影响,而且在这种情况下也无法将肌肉收缩的生化影响和机械影响分离开来,这就促使人们在体外研究这一现象。这项研究证明,调整纤维蛋白的机械特性可以纵向培养高度收缩的骨骼肌单层,从而实现对运动组织的功能表征和长期分泌组采集。用运动肌肉分泌的因子刺激运动神经元,可显著上调神经元的生长和迁移,其效应大小取决于肌肉收缩强度。嵌入纤维蛋白水凝胶中的驱动磁性微粒能够动态拉伸运动神经元,并无创模拟肌肉收缩的机械效应。有趣的是,轴突生成在机械刺激和生化刺激的运动神经元中都有类似的上调,但 RNA 测序揭示了不同组间不同的转录组特征,生化刺激对轴突生成和突触成熟相关的细胞信号传导影响更大。这项研究利用可驱动的细胞外基质,有力地验证了之前假设的肌肉收缩通过机械和生化信号自下而上调节运动神经元生长和成熟的作用。
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来源期刊
Advanced Healthcare Materials
Advanced Healthcare Materials 工程技术-生物材料
CiteScore
14.40
自引率
3.00%
发文量
600
审稿时长
1.8 months
期刊介绍: Advanced Healthcare Materials, a distinguished member of the esteemed Advanced portfolio, has been dedicated to disseminating cutting-edge research on materials, devices, and technologies for enhancing human well-being for over ten years. As a comprehensive journal, it encompasses a wide range of disciplines such as biomaterials, biointerfaces, nanomedicine and nanotechnology, tissue engineering, and regenerative medicine.
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