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Depletion of chondrocyte primary cilia reduces the compressive modulus of articular cartilage

机译:软骨细胞原纤毛的耗竭降低了关节软骨的压缩模量

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摘要

Primary cilia are slender, microtubule based structures found in the majority of cell types with one cilium per cell. In articular cartilage, primary cilia are required for chondrocyte mechanotransduction and the development of healthy tissue. Loss of primary cilia in Col2aCre;ift88fl/fl transgenic mice results in up-regulation of osteoarthritic (OA) markers and development of OA like cartilage with greater thickness and reduced mechanical stiffness. However no previous studies have examined whether loss of primary cilia influences the intrinsic mechanical properties of articular cartilage matrix in the form of the modulus or just the structural properties of the tissue. The present study describes a modified analytical model to derive the viscoelastic moduli based on previous experimental indentation data. Results show that the increased thickness of the articular cartilage in the Col2aCre;ift88fl/fl transgenic mice is associated with a reduction in both the instantaneous and equilibrium moduli at indentation strains of greater than 20%. This reveals that the loss of primary cilia causes a significant reduction in the mechanical properties of cartilage particularly in the deeper zones and possibly the underlying bone. This is consistent with histological analysis and confirms the importance of primary cilia in the development of a mechanically functional articular cartilage.
机译:原发纤毛是细长的,基于微管的结构,存在于大多数细胞类型中,每个细胞一个纤毛。在关节软骨中,软骨细胞机械转导和健康组织发育需要原发纤毛。在Col2aCre; ift88fl / fl转基因小鼠中失去初级纤毛会导致骨关节炎(OA)标志物的上调并导致OA的发展,例如软骨厚度增加,机械刚度降低。然而,以前的研究都没有检查原发纤毛的损失是否以模量或组织的结构性质的形式影响关节软骨基质的固有机械性质。本研究描述了一种修改的分析模型,可以根据先前的实验压痕数据得出粘弹性模量。结果表明,在Col2aCre; ift88fl / fl转基因小鼠中,关节软骨厚度的增加与压痕应变大于20%时的瞬时模量和平衡模量降低有关。这表明,初级纤毛的损失导致软骨的机械特性显着降低,特别是在较深的区域甚至可能在下面的骨骼中。这与组织学分析一致,并证实了原发性纤毛在机械功能性关节软骨发展中的重要性。

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