胶原蛋白网络的力学模型,用于了解老化皮肤破坏特性的变化。

IF 1.7 4区 医学 Q4 BIOPHYSICS Journal of Biomechanical Engineering-Transactions of the Asme Pub Date : 2024-07-01 DOI:10.1115/1.4064406
Nathan J Witt, Alan E Woessner, Jacob Herrmann, Kyle P Quinn, Edward A Sander
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引用次数: 0

摘要

随着年龄的增长,真皮层胶原蛋白的组成和结构会发生变化,从而导致皮肤发生机械性改变。以往的研究结果相互矛盾,有报告称老化皮肤的硬度会增加,也有报告称老化皮肤的硬度会降低。驱动年龄相关变化的潜在结构-功能关系非常复杂,难以单独研究。造成这些变化的一个潜在因素是胶原纤维内非酶交联的积累,它会影响真皮胶原蛋白的重塑和机械性能。具体来说,这些交联使单个纤维在其塑性加载区域变得更硬,并导致胶原蛋白网络的碎裂增加。为了更好地了解这些变化的影响,我们使用代表真皮微观结构的离散纤维网研究了非酶交联变化对真皮微观结构的影响。我们的研究结果表明,增强胶原蛋白塑性区域的机械响应对网络级刚度和破坏应力的影响微乎其微。相反,通过失去连通性来模拟碎裂会大大降低网络刚度和破坏应力,同时增加破坏时的拉伸比。
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Mechanical Models of Collagen Networks for Understanding Changes in the Failure Properties of Aging Skin.

Skin undergoes mechanical alterations due to changes in the composition and structure of the collagenous dermis with aging. Previous studies have conflicting findings, with both increased and decreased stiffness reported for aging skin. The underlying structure-function relationships that drive age-related changes are complex and difficult to study individually. One potential contributor to these variations is the accumulation of nonenzymatic crosslinks within collagen fibers, which affect dermal collagen remodeling and mechanical properties. Specifically, these crosslinks make individual fibers stiffer in their plastic loading region and lead to increased fragmentation of the collagenous network. To better understand the influence of these changes, we investigated the impact of nonenzymatic crosslink changes on the dermal microstructure using discrete fiber networks representative of the dermal microstructure. Our findings suggest that stiffening the plastic region of collagen's mechanical response has minimal effects on network-level stiffness and failure stresses. Conversely, simulating fragmentation through a loss of connectivity substantially reduces network stiffness and failure stress, while increasing stretch ratios at failure.

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来源期刊
CiteScore
3.40
自引率
5.90%
发文量
169
审稿时长
4-8 weeks
期刊介绍: Artificial Organs and Prostheses; Bioinstrumentation and Measurements; Bioheat Transfer; Biomaterials; Biomechanics; Bioprocess Engineering; Cellular Mechanics; Design and Control of Biological Systems; Physiological Systems.
期刊最新文献
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