Li Mi, Xi Ning, Wang Yuechao, Liu Lianqing
Department of Industrial and Manufacturing Systems Engineering, The University of Hong Kong, Kowloon 999077, Hong Kong, China.
ACS Biomater Sci Eng. 2019 Oct 14;5(10):5036-5050. doi: 10.1021/acsbiomaterials.9b00991. Epub 2019 Sep 10.
Cell-substrate interactions play an important role in regulating cellular physiological and pathological processes, and therefore, investigating cell-substrate interface is meaningful for understanding the behaviors of cells. However, so far, the underlying mechanisms which guide the nanoscopic biological activities taking place at the cell-substrate interface remain poorly understood. The advent of atomic force microscopy (AFM) provides a powerful tool for characterizing the structures and properties of native biological and biomaterial systems with unprecedented spatiotemporal resolution, which offers new possibilities for understanding the physical sciences of biomaterials. Here, AFM was utilized to unravel the nanotopographical surfaces for regulating cellular behaviors on three different substrates (glass slide, mica, and Petri dish). First, the decellularized substrates prepared with the use of ammonia and trypsin were imaged by AFM, significantly showing the nanogranular substances on the decellularized substrates as well as the cell membrane patches for uncovering the detailed situations of mechanical contact between cells and substrates. Next, experiments performed on chemically fixed substrates with the use of paraformaldehyde together with AFM time-lapse imaging remarkably showed that nanogranular depositions from the cell culture medium appeared on the substrates for promoting cell growth. Further, the detailed cell culture medium components which contribute to the nanogranular depositions are identified. Finally, the dynamic alterations in surface roughness and mechanical properties of substrates and cells during cell growth were quantitatively measured by AFM, revealing the diverse changes of the multiple physical properties (surface roughness, adhesion force, Young's modulus, and relaxation time) during cell-substrate interactions. The research provides novel insights into the nanotopographical surfaces for cell-substrate interactions, which will be useful for understanding cellular behaviors.
细胞与底物的相互作用在调节细胞生理和病理过程中起着重要作用,因此,研究细胞与底物界面对于理解细胞行为具有重要意义。然而,迄今为止,指导细胞与底物界面发生的纳米级生物活性的潜在机制仍知之甚少。原子力显微镜(AFM)的出现提供了一种强大的工具,以前所未有的时空分辨率表征天然生物和生物材料系统的结构和特性,这为理解生物材料的物理科学提供了新的可能性。在此,利用AFM揭示了三种不同底物(载玻片、云母和培养皿)上调节细胞行为的纳米拓扑表面。首先,用氨和胰蛋白酶制备的脱细胞底物通过AFM成像,显著显示了脱细胞底物上的纳米颗粒物质以及细胞膜斑块,以揭示细胞与底物之间机械接触的详细情况。接下来,使用多聚甲醛对化学固定的底物进行实验,并结合AFM延时成像,结果显著表明细胞培养基中的纳米颗粒沉积物出现在促进细胞生长的底物上。此外,还确定了导致纳米颗粒沉积的详细细胞培养基成分。最后,通过AFM定量测量了细胞生长过程中底物和细胞表面粗糙度和力学性能的动态变化,揭示了细胞与底物相互作用过程中多种物理性质(表面粗糙度、粘附力、杨氏模量和弛豫时间)的不同变化。该研究为细胞与底物相互作用的纳米拓扑表面提供了新的见解,这将有助于理解细胞行为。