INM - Leibniz Institute for New Materials, Saarbrücken, Germany,
Pharmacelsus GmbH, Saarbrücken, Germany.
Int J Nanomedicine. 2019 Feb 22;14:1411-1431. doi: 10.2147/IJN.S189888. eCollection 2019.
Nanoparticles (NPs) are used in numerous products in technical fields and biomedicine; their potential adverse effects have to be considered in order to achieve safe applications. Besides their distribution in tissues, organs, and cellular localization, their impact and penetration during the process of tissue formation occurring in vivo during liver regeneration are critical steps for establishment of safe nanomaterials.
In this study, 3D cell culture of human hepatocarcinoma cells (HepG2) was used to generate cellular spheroids, serving as in vitro liver microtissues. In order to determine their differential distribution and penetration depth in HepG2 spheroids, SiO NPs were applied either during or after spheroid formation. The NP penetration was comprehensively studied using confocal laser scanning microscopy and scanning electron microscopy.
Spheroids were exposed to 100 µg mL SiO NPs either at the beginning of spheroid formation, or during or after formation of spheroids. Microscopy analyses revealed that NP penetration into the spheroid is limited. During and after spheroid formation, SiO NPs penetrated about 20 µm into the spheroids, corresponding to about three cell layers. In contrast, because of the addition of SiO NPs simultaneously to cell seeding, NP agglomerates were located also in the spheroid center. Application of SiO NPs during the process of spheroid formation had no impact on final spheroid size.
Understanding the distribution of NPs in tissues is essential for biomedical applications. The obtained results indicate that NPs show only limited penetration into already formed tissue, which is probably caused by the alteration of the tissue structure and cell packing density during the process of spheroid formation.
纳米粒子(NPs)在技术领域和生物医学领域的众多产品中得到广泛应用;为了实现安全应用,必须考虑它们的潜在不良影响。除了在组织、器官中的分布和细胞定位外,它们在体内肝再生过程中组织形成过程中的影响和穿透也是建立安全纳米材料的关键步骤。
本研究采用人肝癌细胞(HepG2)的 3D 细胞培养来生成细胞球体,作为体外肝微组织。为了确定 SiO NPs 在 HepG2 球体中的差异分布和穿透深度,在球体形成过程中或之后应用 SiO NPs。使用共聚焦激光扫描显微镜和扫描电子显微镜对 NP 穿透进行了全面研究。
球体在开始形成时、形成过程中或之后暴露于 100 µg mL 的 SiO NPs 中。显微镜分析表明 NP 穿透球体的能力有限。在形成过程中和之后,SiO NPs 穿透到球体中约 20 µm,相当于大约三个细胞层。相比之下,由于 SiO NPs 同时添加到细胞接种中,NP 团聚体也位于球体中心。在球体形成过程中添加 SiO NPs 对最终球体大小没有影响。
了解 NP 在组织中的分布对于生物医学应用至关重要。所得结果表明,NP 仅在有限的程度上穿透已形成的组织,这可能是由于球体形成过程中组织结构和细胞堆积密度的改变所致。