单独的生物形态弹性:在没有有限应变的情况下模拟烧伤后收缩和肥厚的局限性。

IF 2.7 3区 医学 Q2 BIOPHYSICS
Ginger Egberts, Fred Vermolen, Paul van Zuijlen
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引用次数: 0

摘要

我们提出了一个基于连续体假设的二维生物形态弹性模型,描述烧伤后疤痕的肥大和收缩。该模型基于永久性变形的形态弹性,并结合了包含细胞密度、胶原蛋白密度和化学引诱剂浓度的化学生物学模型。我们对模型的独立参数进行了敏感性分析,并重点研究了低肌成纤维细胞凋亡率对烧伤后皮肤厚度特征的影响。我们得出结论,最敏感的参数是平衡胶原浓度、信号分子分泌速率和细胞力常数,并将这些结果与稳定性约束联系起来。接下来,我们观察了模拟收缩和肥大之间的关系,并显示了肌成纤维细胞凋亡率(高/低)的显著变化的影响。我们的最终目标是通过开发具有高度确定性的预测模型来优化烧伤后的治疗。我们认为提出的模型和敏感性分析是迈向它们的一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biomorphoelasticity alone: limitations in modeling post-burn contraction and hypertrophy without finite strains.

We present a continuum hypothesis-based two-dimensional biomorphoelastic model describing post-burn scar hypertrophy and contraction. The model is based on morphoelasticity for permanent deformations and combined with a chemical-biological model that incorporates cellular densities, collagen density, and the concentration of chemoattractants. We perform a sensitivity analysis for the independent parameters of the model and focus on the effects on the features of the post-burn dermal thickness given a low myofibroblast apoptosis rate. We conclude that the most sensitive parameters are the equilibrium collagen concentration, the signaling molecule secretion rate and the cell force constant, and link these results to stability constraints. Next, we observe a relationship between the simulated contraction and hypertrophy and show the effects for significant variations in the myofibroblast apoptosis rate (high/low). Our ultimate goal is to optimize post-burn treatments, by developing models that predict with a high degree of certainty. We consider the presented model and sensitivity analysis to be a step toward their construction.

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来源期刊
Biomechanics and Modeling in Mechanobiology
Biomechanics and Modeling in Mechanobiology 工程技术-工程:生物医学
CiteScore
7.10
自引率
8.60%
发文量
119
审稿时长
6 months
期刊介绍: Mechanics regulates biological processes at the molecular, cellular, tissue, organ, and organism levels. A goal of this journal is to promote basic and applied research that integrates the expanding knowledge-bases in the allied fields of biomechanics and mechanobiology. Approaches may be experimental, theoretical, or computational; they may address phenomena at the nano, micro, or macrolevels. Of particular interest are investigations that (1) quantify the mechanical environment in which cells and matrix function in health, disease, or injury, (2) identify and quantify mechanosensitive responses and their mechanisms, (3) detail inter-relations between mechanics and biological processes such as growth, remodeling, adaptation, and repair, and (4) report discoveries that advance therapeutic and diagnostic procedures. Especially encouraged are analytical and computational models based on solid mechanics, fluid mechanics, or thermomechanics, and their interactions; also encouraged are reports of new experimental methods that expand measurement capabilities and new mathematical methods that facilitate analysis.
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