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Substrate Stiffness Regulates the Development of Left-Right Asymmetry in Cell Orientation

机译:基板刚度调节细胞方向中左右不对称的发展

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Left-right (LR) asymmetry of tissue/organ structure is a morphological feature essential for many tissue functions. The ability to incorporate the LR formation in constructing tissue/organ replacement is important for recapturing the inherent tissue structure and functions. However, how LR asymmetry is formed remains largely underdetermined, which creates significant hurdles to reproduce and regulate the formation of LR asymmetry in an engineering context. Here, we report substrate rigidity functioning as an effective switch that turns on the development of LR asymmetry. Using micropatterned cell-adherent stripes on rigid substrates, we found that cells collectively oriented at a LR-biased angle relative to the stripe boundary. This LR asymmetry was initiated by a LR-biased migration of cells at stripe boundary, which later generated a velocity gradient propagating from stripe boundary to the center. After a series of cell translocations and rotations, ultimately, an LR-biased cell orientation within the micropatterned stripe was formed. Importantly, this initiation and propagation of LR asymmetry was observed only on rigid but not on soft substrates, suggesting that the LR asymmetry was regulated by rigid substrate probably through the organization of actin cytoskeleton. Together, we demonstrated substrate rigidity as a determinant factor that mediates the self-organizing LR asymmetry being unfolded from single cells to multicellular organization. More broadly, we anticipate that our findings would pave the way for rebuilding artificial tissue constructs with inherent LR asymmetry in the future.
机译:组织/器官结构的左右(LR)不对称是许多组织功能必不可少的形态特征。在构造组织/器官替代物中整合LR形成的能力对于重新获得固有的组织结构和功能很重要。但是,LR不对称的形成方式仍未确定,这在工程环境中为再现和调节LR不对称的形成创造了重大障碍。在这里,我们报告了基板刚度起着有效开关的作用,该开关开启了LR不对称的发展。在刚性基板上使用微图案的细胞粘附条纹,我们发现细胞集体相对于条纹边界以LR偏向取向。这种LR不对称性是由条带边界处的LR偏向细胞迁移引起的,该迁移随后产生了从条带边界传播到中心的速度梯度。经过一系列的细胞移位和旋转后,最终,在微图案条纹内形成了偏向LR的细胞方向。重要的是,LR不对称性的这种起始和传播仅在刚性底物上观察到,而在软质基质上则未观察到,这表明LR不对称性可能是由刚性底物通过肌动蛋白细胞骨架的组织来调节的。在一起,我们证明了基板刚度作为决定因素,介导自单细胞向多细胞组织发展的自组织LR不对称性。更广泛地说,我们预期我们的发现将为将来重建具有固有LR不对称性的人工组织构造铺平道路。

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