Variability in individual native fibrin fiber mechanics.

IF 2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Physical biology Pub Date : 2024-10-30 DOI:10.1088/1478-3975/ad899f
Christine C Helms
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Abstract

Fibrin fibers are important structural elements in blood coagulation. They form a mesh network that acts as a scaffold and imparts mechanical strength to the clot. A review of published work measuring the mechanics of fibrin fibers reveals a range of values for fiber extensibility. This study investigates fibrinogen concentration as a variable responsible for variability in fibrin mechanics. It expands previous work to describe the modulus, strain hardening, extensibility, and the force required for fiber failure when fibers are formed with different fibrinogen concentrations using lateral force atomic force microscopy. Analysis of the mechanical properties showed fibers formed from 1 mg ml-1and 2 mg ml-1fibrinogen had significantly different mechanical properties. To help clarify our findings we developed two behavior profiles to describe individual fiber mechanics. The first describes a fiber with low initial modulus and high extensible, that undergoes significant strain hardening, and has moderate strength. Most fibers formed with 1 mg ml-1fibrinogen had this behavior profile. The second profile describes a fiber with a high initial modulus, minimal strain hardening, high strength, and low extensibility. Most fibrin fibers formed with 2 mg ml-1fibrinogen were described by this second profile. In conclusion, we see a range of behaviors from fibers formed from native fibrinogen molecules but various fibrinogen concentrations. Potential differences in fiber formation are investigated with SEM. It is likely this range of behaviors also occursin vivo. Understanding the variability in mechanical properties could contribute to a deeper understanding of pathophysiology of coagulative disorders.

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单个原生纤维蛋白纤维力学的变异性
纤维蛋白纤维是血液凝固过程中的重要结构元素。它们形成的网状结构起到支架的作用,并赋予血凝块机械强度。对已发表的纤维蛋白纤维力学测量工作进行回顾后发现,纤维延伸性的数值范围不一。本研究将纤维蛋白原浓度作为导致纤维蛋白力学变化的一个变量进行研究。它扩展了之前的工作,利用横向力原子力显微镜描述了不同浓度纤维蛋白原形成纤维时的模量、应变硬化、延伸性和纤维断裂所需的力。机械性能分析表明,1 毫克/毫升和 2 毫克/毫升纤维蛋白原形成的纤维具有明显不同的机械性能。为了帮助澄清我们的发现,我们开发了两种行为曲线来描述单个纤维的力学特性。第一种描述的是初始模量低、可延展性高的纤维,这种纤维会发生明显的应变硬化,并具有中等强度。使用 1 毫克/毫升纤维蛋白原形成的大多数纤维都具有这种行为特征。第二种纤维具有高初始模量、最小应变硬化、高强度和低延伸性。大多数使用 2 毫克/毫升纤维蛋白原形成的纤维蛋白纤维都具有第二种特征。总之,我们可以看到由原生纤维蛋白原分子和不同浓度的纤维蛋白原形成的纤维具有不同的行为。用扫描电镜研究了纤维形成的潜在差异。这一系列行为很可能也发生在体内。了解机械性能的变化有助于深入理解凝血障碍的病理生理学。
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来源期刊
Physical biology
Physical biology 生物-生物物理
CiteScore
4.20
自引率
0.00%
发文量
50
审稿时长
3 months
期刊介绍: Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity. Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as: molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division systems biology, e.g. signaling, gene regulation and metabolic networks cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis cell-cell interactions, cell aggregates, organoids, tissues and organs developmental dynamics, including pattern formation and morphogenesis physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation neuronal systems, including information processing by networks, memory and learning population dynamics, ecology, and evolution collective action and emergence of collective phenomena.
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