Influence of Radial Variations in Biochemical Concentrations in Collagen Type and Water on Mechanical Stability of Annulus Fibrosus' Collagen-Hyaluronan Interfaces at Nanoscale: A Molecular Dynamics Investigation.

IF 1.7 4区 医学 Q4 BIOPHYSICS
Shambo Bhattacharya, Devendra Kumar Dubey
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引用次数: 0

Abstract

Multidirectional load transmission ability by Annulus Fibrosus (AF) require substantial mechanical stability. Additionally, AF exhibits a unique biochemical concentration gradient with outer AF (OA) dominated by type I collagen (COL-I) and inner AF dominated by type II collagen (COL-II) with higher water and proteoglycan concentration. This indicates an intricate relationship between biochemistry and mechanical stability, which remains unclear. This study uses molecular dynamics simulations to investigate the impact of water, COL-I and COL-II, concentration gradients on mechanical stability of AF's Collagen-Hyaluronan nanointerfaces during tensile and compressive deformation. For this, COL-HYL atomistic models are created by increasing COL-II concentrations from 0% to 75%, and water from 65% to 75%. Additional simulation is conducted by increasing water concentration of COL-I-HYL interface (0% COL-II) to 75% to segregate water concentration variation effects. Results show increasing water concentration to 75% results in marginal changes in local hydration indicating increase in bulk water. This enhances HYL and COL segment sliding - leading to reduction in mechanical stability in tension, indicated by drop in stress-strain characteristics. Additionally, increase in bulk water shifts load bearing characteristics towards water - leading to reduction in modulus from 3.7 GPa to 1.9 GPa. Conversely, increasing COL-II and water concentration facilitates stable water bridge formation which impede sliding in HYL and COL - enhancing mechanical stability. These water bridges improve compressive load sustenance leading to lower reduction in compressive modulus from 3.7 GPa to 2.8 GPa.

胶原类型和水的生化浓度径向变化对纳米尺度纤维环胶原-透明质酸界面机械稳定性的影响:分子动力学研究。
椎间盘纤维环(AF)的多向负荷传递能力需要很强的机械稳定性。此外,AF 还表现出独特的生化浓度梯度,外层 AF(OA)以 I 型胶原蛋白(COL-I)为主,而内层 AF 则以 II 型胶原蛋白(COL-II)为主,并含有较高的水和蛋白多糖浓度。这表明生物化学与机械稳定性之间存在着错综复杂的关系,而这种关系目前仍不清楚。本研究利用分子动力学模拟来研究水、COL-I 和 COL-II 浓度梯度对 AF 的胶原-透明质酸纳米界面在拉伸和压缩变形过程中的机械稳定性的影响。为此,我们创建了 COL-HYL 原子模型,将 COL-II 浓度从 0% 增加到 75%,将水从 65% 增加到 75%。此外,还将 COL-I-HYL 界面(COL-II 浓度为 0%)的水浓度提高到 75%,以隔离水浓度变化的影响。结果表明,将水浓度提高到 75% 会导致局部水化发生微小变化,表明体积水增加。这增强了 HYL 和 COL 段的滑动--导致拉伸机械稳定性降低,表现为应力应变特性下降。此外,体积水的增加使承载特性向水转移,导致模量从 3.7 GPa 降至 1.9 GPa。相反,增加 COL-II 和水的浓度有利于形成稳定的水桥,从而阻碍 HYL 和 COL 的滑动,提高机械稳定性。这些水桥提高了抗压负荷的承受能力,从而降低了抗压模量,从 3.7 GPa 降至 2.8 GPa。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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.
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