Structural determinants of tendon multiscale mechanics and their sensitivity to mechanical stimulation during development in an embryonic chick model

IF 9.4 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Benjamin E. Peterson , Maria L. Canonicco Castro , Helen O. McCarthy , Niamh Buckley , Nicholas Dunne , Rebecca A. Rolfe , Paula Murphy , Spencer E. Szczesny
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引用次数: 0

Abstract

There is an abrupt increase in the multiscale mechanical properties and load-bearing capabilities of tendon during development. While prior work has identified numerous changes that occur within the collagenous structure during this developmental period, the primary structural elements that give rise to this abrupt increase in mechanical functionality, and their mechanobiological sensitivity, remain unclear. To address this knowledge gap, we used a shear lag model along with ultrastructural imaging, biochemical/thermodynamic assays, and multiscale mechanical testing to investigate the dynamic structure-function relationships during late-stage embryonic chick development and to establish their sensitivity to mechanical stimulation. Mechanical testing and modeling suggested that the rapid increase in multiscale mechanics can be explained by increases in fibril length, intrafibrillar crosslinking, and fibril area fraction. To partially test this, we inhibited collagen crosslinking during development and observed a drastic reduction in multiscale mechanical behavior that was explained by a reduction in both fibril modulus and length. Using muscle paralysis to investigate mechanosensitivity, we observed a significantly impaired multiscale mechanical response despite minimal changes in fibril diameter and fibril area fraction. Additionally, the shear lag model found a trend toward lower fibril lengths with paralysis and experimental data found decreased crosslinking and fibril modulus values following flaccid paralysis. Together, these data suggest that both intrafibrillar crosslink formation and fibril elongation are critical to the formation of load-bearing capabilities in tenogenesis and are sensitive to mechanical loading. These findings provide critical insights into the biological and structural mechanisms that give rise to tensile load-bearing soft tissue.

Statement of Significance

Despite prior work investigating the structural and mechanical changes that occur during tendon development, there has not been a comprehensive analysis of how these simultaneous changes in structure and function are connected. In this study, we performed a comprehensive battery of mechanical and structural assessments of embryonic chick tendons and input these data into a shear lag model to estimate the individual importance of each structural change to the tendon mechanical properties. Additionally, we inhibited muscle activity in the embryos to evaluate the impact of mechanical stimulation on these evolving structure-function relationships during tendon development. These data provide insight into the primary structural elements that produce the tensile load-bearing capabilities of tendon, which will inform efforts to produce tissue engineered tendon replacements.

Abstract Image

胚胎雏鸡模型发育过程中肌腱多尺度力学的结构决定因素及其对机械刺激的敏感性
在胚胎发育过程中,肌腱的多尺度机械性能和承重能力会突然增加。虽然之前的工作已经确定了在这一发育阶段胶原结构发生的许多变化,但导致机械功能突然增加的主要结构元素及其机械生物学敏感性仍不清楚。为了填补这一知识空白,我们利用剪切滞后模型、超微结构成像、生化/热力学实验和多尺度机械测试来研究胚胎后期小鸡发育过程中的动态结构-功能关系,并确定它们对机械刺激的敏感性。力学测试和建模表明,纤维长度、纤维内交联和纤维面积分数的增加可以解释多尺度力学的快速增长。为了部分验证这一点,我们在发育过程中抑制了胶原交联,观察到多尺度力学行为急剧下降,这可以用纤维模量和长度的减少来解释。利用肌肉瘫痪来研究机械敏感性,我们观察到,尽管纤维直径和纤维面积分数变化极小,但多尺度机械响应却明显受损。此外,剪切滞后模型发现瘫痪后纤维长度有降低的趋势,实验数据发现瘫痪后交联和纤维模量值降低。这些数据共同表明,纤维内交联的形成和纤维的伸长对韧带生成过程中承载能力的形成至关重要,并且对机械负荷很敏感。这些发现为了解产生拉伸承重软组织的生物和结构机制提供了重要依据。意义说明:尽管之前有研究对肌腱发育过程中发生的结构和机械变化进行了研究,但还没有对这些结构和功能的同步变化之间的联系进行全面分析。在这项研究中,我们对胚胎雏鸡肌腱进行了全面的机械和结构评估,并将这些数据输入剪切滞后模型,以估算每种结构变化对肌腱机械特性的重要性。此外,我们还抑制了胚胎中的肌肉活动,以评估机械刺激对肌腱发育过程中结构-功能演变的影响。这些数据让我们深入了解了产生肌腱拉伸承载能力的主要结构元素,这将为生产组织工程肌腱替代品提供参考。
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来源期刊
Acta Biomaterialia
Acta Biomaterialia 工程技术-材料科学:生物材料
CiteScore
16.80
自引率
3.10%
发文量
776
审稿时长
30 days
期刊介绍: Acta Biomaterialia is a monthly peer-reviewed scientific journal published by Elsevier. The journal was established in January 2005. The editor-in-chief is W.R. Wagner (University of Pittsburgh). The journal covers research in biomaterials science, including the interrelationship of biomaterial structure and function from macroscale to nanoscale. Topical coverage includes biomedical and biocompatible materials.
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