Jia Yuanbo, Wang Yanzhong, Niu Lele, Zhang Hang, Tian Jin, Gao Dengfeng, Zhang Xiaohui, Lu Tian Jian, Qian Jin, Huang Guoyou, Xu Feng
The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, 710049, P. R. China.
Bioinspired Engineering and Biomechanics Center (BEBC), Xi'an Jiaotong University, Xi'an, 710049, P. R. China.
Adv Healthc Mater. 2021 Apr;10(8):e2001856. doi: 10.1002/adhm.202001856. Epub 2021 Jan 29.
Natural extracellular matrix (ECM) mostly has a fibrous structure that supports and mechanically interacts with local residing cells to guide their behaviors. The effect of ECM elasticity on cell behaviors has been extensively investigated, while less attention has been paid to the effect of matrix fiber-network plasticity at microscale, although plastic remodeling of fibrous matrix is a common phenomenon in fibrosis. Here, a significant decrease is found in plasticity of native fibrotic tissues, which is associated with an increase in matrix crosslinking. To explore the role of plasticity in fibrosis development, a set of 3D collagen nanofibrous matrix with constant modulus but tunable plasticity is constructed by adjusting the crosslinking degree. Using plasticity-controlled 3D culture models, it is demonstrated that the decrease of matrix plasticity promotes fibroblast activation and spreading. Further, a coarse-grained molecular dynamic model is developed to simulate the cell-matrix interaction at microscale. Combining with molecular experiments, it is revealed that the enhanced fibroblast activation is mediated through cytoskeletal tension and nuclear translocation of Yes-associated protein. Taken together, the results clarify the effects of crosslinking-induced plasticity changes of nanofibrous matrix on the development of fibrotic diseases and highlight plasticity as an important mechanical cue in understanding cell-matrix interactions.
天然细胞外基质(ECM)大多具有纤维结构,可支持局部驻留细胞并与之发生机械相互作用,以引导其行为。ECM弹性对细胞行为的影响已得到广泛研究,而在微观尺度上,基质纤维网络可塑性的影响却较少受到关注,尽管纤维基质的塑性重塑在纤维化过程中是一种常见现象。在此,研究发现天然纤维化组织的可塑性显著降低,这与基质交联增加有关。为了探究可塑性在纤维化发展中的作用,通过调节交联度构建了一组具有恒定模量但可塑性可调的三维胶原纳米纤维基质。利用可塑性控制的三维培养模型,研究表明基质可塑性的降低会促进成纤维细胞的激活和铺展。此外,还建立了一个粗粒度分子动力学模型来模拟微观尺度上的细胞-基质相互作用。结合分子实验发现,成纤维细胞激活增强是通过细胞骨架张力和Yes相关蛋白的核转位介导的。综上所述,这些结果阐明了纳米纤维基质交联诱导的可塑性变化对纤维化疾病发展的影响,并强调可塑性是理解细胞-基质相互作用的重要力学线索。