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Primary Cilium Mechanotransduction of Tensile Strain in 3D Culture: Finite Element Analyses of Strain Amplification Caused by 10 Tensile Strain Applied to a Primary Cilium Embedded in a Collagen Matrix

机译:在3D文化中拉伸菌株的初级Cichan机械转导:应用于胶原基质中嵌入的初级Cilium的10%拉伸菌株引起的菌株扩增的有限元分析。

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摘要

Human adipose-derived stem cells (hASC) exhibit multilineage differentiation potential with lineage specification that is dictated by both the chemical and mechanical stimuli to which they are exposed. We have previously shown that 10% cyclic tensile strain increases hASC osteogenesis and cell-mediated calcium accretion. We have also recently shown that primary cilia are present on hASC and that chemically-induced lineage specification of hASC concurrently results in length and conformation changes of the primary cilia. Further, we have observed cilia length changes on hASC cultured within a collagen I gel in response to 10% cyclic tensile strain. We therefore hypothesize that primary cilia may play a key mechanotransduction role for hASC exposed to tensile strain. The goal of this study was to use finite element analysis (FEA) to determine strains occurring within the ciliary membrane in response to 10% tensile strain applied parallel, or perpendicular, to cilia orientation. To elucidate the mechanical environment experienced by the cilium, several lengths were modeled and evaluated based on cilia lengths measured on hASC grown under varied culture conditions. Principal tensile strains in both hASC and ciliary membranes were calculated using FEA, and the magnitude and location of maximum principal tensile strain determined. We found that maximum principal tensile strain was concentrated at the base of the cilium. In the linear elastic model, applying strain perpendicular to the cilium resulted in maximum strains within the ciliary membrane from 150 to 200%, while applying strain parallel to the cilium resulted in much higher strains, approximately 400%. In the hyperelastic model, applying strain perpendicular to the cilium resulted in maximum strains within the ciliary membrane around 30%, while applying strain parallel to the cilium resulted in much higher strains ranging from 50% to 70% . Interestingly, FEA results indicated that primary cilium length was not directly related to ciliary membrane strain. Rather, it appears that cilium orientation may be more important than cilium length in determining sensitivity of hASC to tensile strain. This is the first study to model the effects of tensile strain on the primary cilium and provides newfound insight into the potential role of the primary cilium as a mechanosensor, particularly in tensile strain and potentially a multitude of other mechanical stimuli beyond fluid shear.
机译:人脂肪来源的干细胞(hASC)具有多种谱系分化潜能,其谱系规格受它们所受到的化学和机械刺激的支配。先前我们已经表明10%的循环拉伸应变会增加hASC的成骨作用和细胞介导的钙积聚。我们最近还显示,原发纤毛存在于hASC上,并且化学诱导的hASC谱系规范同时导致原发纤毛的长度和构象变化。此外,我们已经观察到胶原蛋白I凝胶中培养的hASC的纤毛长度响应10%循环拉伸应变而变化。因此,我们假设原发纤毛可能对暴露于拉伸应变的hASC发挥关键的机械转导作用。这项研究的目的是使用有限元分析(FEA)来确定响应于平行或垂直于纤毛取向的10%拉伸应变在睫状膜内发生的应变。为了阐明纤毛所经历的机械环境,基于在不同培养条件下生长的hASC测得的纤毛长度,对几种长度进行了建模和评估。使用FEA计算hASC和睫状膜中的主拉伸应变,并确定最大主拉伸应变的大小和位置。我们发现最大主拉伸应变集中在纤毛的底部。在线性弹性模型中,施加垂直于纤毛的应变会导致睫状膜内的最大应变为150%至200%,而施加平行于纤毛的应变会产生更高的应变,约为400%。在超弹性模型中,施加垂直于纤毛的应变会导致睫状膜内的最大应变约为30%,而施加平行于纤毛的应变会产生更高的应变,范围为50%至70%。有趣的是,FEA结果表明初级纤毛长度与睫状膜应变没有直接关系。相反,在确定hASC对拉伸应变的敏感性时,纤毛方向似乎比纤毛长度更重要。这是首次模拟拉伸应变对初级纤毛的影响的研究,并提供了有关初级纤毛作为机械传感器的潜在作用的新见解,特别是在拉伸应变和流体剪切以外的其他多种机械刺激方面。

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