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用于检测电子控制模块(ECM)残余应变的电机离合器模型的见解。

Insight to motor clutch model for sensing of ECM residual strain.

作者信息

Panzetta Valeria, De Clemente Claudia, Russo Michele, Fusco Sabato, Netti Paolo A

机构信息

Department of Chemical, Materials and Production Engineering, University of Naples Federico II, 80125, Naples, Italy.

Centro di Ricerca Interdipartimentale sui Biomateriali, University of Naples Federico II, 80125, Naples, Italy.

出版信息

Mechanobiol Med. 2023 Oct 12;1(2):100025. doi: 10.1016/j.mbm.2023.100025. eCollection 2023 Dec.

Abstract

The mechanical microenvironment strongly affects cell state and decisions. Cell mechanosensing has been described by a which gets progressively engaged depending upon the stiffness of the extracellular material. Through the actuation of pulling forces exerted by actin fibres on the mechanosensitive talin-integrin molecular complex, cells sense and react to the stiffness of their surroundings. However, whether the truly cell mechanosensing is regulated by the pure elastic stiffness or by the strain energy density of the ECM is still debated. Here we report that the cell response to change of strain energy density out of loading induced deformation (purely elastic) can be accounted for by including, within the same frame of the molecular clutch model, the residual strain/stress to which the ECM could be subjected before establishing any interaction with the molecular clutches. To include the contribution of residual stresses, an additional spring orthogonal to the ones already present in the original clutch model has been introduced; this spring takes memory of the ECM strain energy when axially deformed before any interaction with cell molecular clutches can occur. To evaluate the influence of strain on the optimum number of clutches, the model has been implemented with different levels of strain. Results suggest that cells undergo a reinforcement process, stiffening the cytoskeleton in response to the ECM stress/strain energy.

摘要

机械微环境强烈影响细胞状态和决策。细胞机械传感已被描述为一种机制,它根据细胞外材料的硬度逐渐被激活。通过肌动蛋白纤维对机械敏感的踝蛋白 - 整合素分子复合物施加拉力,细胞感知并对周围环境的硬度做出反应。然而,真正的细胞机械传感是由纯弹性硬度还是由细胞外基质的应变能密度调节仍存在争议。在这里,我们报告细胞对加载诱导变形(纯弹性)之外的应变能密度变化的反应可以通过在分子离合器模型的同一框架内纳入细胞外基质在与分子离合器建立任何相互作用之前可能承受的残余应变/应力来解释。为了纳入残余应力的贡献,在原始离合器模型中已有的弹簧之外引入了一个额外的正交弹簧;这个弹簧在与细胞分子离合器发生任何相互作用之前轴向变形时会记住细胞外基质的应变能。为了评估应变对最佳离合器数量的影响,该模型已在不同应变水平下实施。结果表明,细胞会经历一个强化过程,响应细胞外基质的应力/应变能而使细胞骨架变硬。

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