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氮化硼纳米管介导的微工程水凝胶上细胞共培养的刺激。

Boron nitride nanotube-mediated stimulation of cell co-culture on micro-engineered hydrogels.

机构信息

The BioRobotics Institute, Scuola Superiore Sant'Anna, Pontedera, Pisa, Italy.

出版信息

PLoS One. 2013 Aug 14;8(8):e71707. doi: 10.1371/journal.pone.0071707. eCollection 2013.

DOI:10.1371/journal.pone.0071707
PMID:23977119
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3743765/
Abstract

In this paper, we describe the effects of the combination of topographical, mechanical, chemical and intracellular electrical stimuli on a co-culture of fibroblasts and skeletal muscle cells. The co-culture was anisotropically grown onto an engineered micro-grooved (10 µm-wide grooves) polyacrylamide substrate, showing a precisely tuned Young's modulus (∼ 14 kPa) and a small thickness (∼ 12 µm). We enhanced the co-culture properties through intracellular stimulation produced by piezoelectric nanostructures (i.e., boron nitride nanotubes) activated by ultrasounds, thus exploiting the ability of boron nitride nanotubes to convert outer mechanical waves (such as ultrasounds) in intracellular electrical stimuli, by exploiting the direct piezoelectric effect. We demonstrated that nanotubes were internalized by muscle cells and localized in both early and late endosomes, while they were not internalized by the underneath fibroblast layer. Muscle cell differentiation benefited from the synergic combination of topographical, mechanical, chemical and nanoparticle-based stimuli, showing good myotube development and alignment towards a preferential direction, as well as high expression of genes encoding key proteins for muscle contraction (i.e., actin and myosin). We also clarified the possible role of fibroblasts in this process, highlighting their response to the above mentioned physical stimuli in terms of gene expression and cytokine production. Finally, calcium imaging-based experiments demonstrated a higher functionality of the stimulated co-cultures.

摘要

本文描述了地形、机械、化学和细胞内电刺激对成纤维细胞和骨骼肌细胞共培养物的影响。共培养物在工程化的微槽(10 µm 宽的槽)聚丙烯酰胺基质上各向异性生长,表现出精确调节的杨氏模量(14 kPa)和较小的厚度(12 µm)。我们通过超声激活的压电纳米结构(即氮化硼纳米管)产生的细胞内刺激来增强共培养物的特性,从而利用氮化硼纳米管将外部机械波(如超声波)转化为细胞内电刺激的能力,利用直接压电效应。我们证明了纳米管被肌肉细胞内化,并定位于早期和晚期内体中,而在下面的成纤维细胞层中没有被内化。肌肉细胞分化受益于地形、机械、化学和基于纳米粒子的刺激的协同组合,表现出良好的肌管发育和向优先方向的对齐,以及编码肌肉收缩关键蛋白(即肌动蛋白和肌球蛋白)的基因的高表达。我们还阐明了成纤维细胞在这个过程中的可能作用,突出了它们对上述物理刺激的基因表达和细胞因子产生的反应。最后,基于钙成像的实验证明了受刺激的共培养物具有更高的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/505b/3743765/6c3d8142f3b6/pone.0071707.g011.jpg
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