Tarhan Tuba, Şen Özlem, Ciofani Melis Emanet, Yılmaz Deniz, Çulha Mustafa
Genetics and Bioengineering Department, Faculty of Engineering, Yeditepe University, Ataşehir, Istanbul, 34755, Turkey; Mardin Artuklu University, Vocational High School of Health Services, 47100, Mardin, Turkey.
Genetics and Bioengineering Department, Faculty of Engineering, Yeditepe University, Ataşehir, Istanbul, 34755, Turkey.
J Trace Elem Med Biol. 2021 Sep;67:126774. doi: 10.1016/j.jtemb.2021.126774. Epub 2021 May 7.
Wound healing is an essential physiological process involving many cell types and their products acting in a marvellous harmony to repair damaged tissues. During the healing process, cellular proliferation and extracellular matrix remodelling stages could be interrupted by undesired factors including microorganisms and altered metabolic activities. In such a case, the process requires some external stimulants to accelerate or remediate the healing stages.
In this study, we report a multifunctional wound healing stimulating agent. In this context, hexagonal boron nitride (hBN) nanoparticles, silver nanoparticles (AgNPs) and polydopamine(pdopa) were used through mussel-inspired chemistry of dopamine to obtain pdopa coated hBN (hBN@pdopa) and AgNPs decorated hBN@pdopa (hBN@pdopa-AgNPs). These two nanostructures were investigated to observe stages of healing.
AgNPs were chosen for inflammation reduction and hBN for induced cell proliferation and migration. In in vitro experiments, firstly, high cellular uptake capacity and biocompatibility of hBN@pdopa and hBN@pdopa-AgNPs were evaluated. They were also tested for their reaction against increased concentration of reactive oxygen species (ROS) in injured cells. Finally, their effect on cellular migration, intracellular tube formation and F-actin organization were monitored by light and confocal microscopy, respectively.
The results clearly indicate that the hBN@pdopa-AgNPs significantly decrease ROS production, promote wound closure, and reorganize tube formation in cells.
伤口愈合是一个重要的生理过程,涉及多种细胞类型及其产物以奇妙的协同作用修复受损组织。在愈合过程中,细胞增殖和细胞外基质重塑阶段可能会被包括微生物和代谢活动改变在内的不良因素打断。在这种情况下,该过程需要一些外部刺激来加速或修复愈合阶段。
在本研究中,我们报道了一种多功能伤口愈合刺激剂。在此背景下,通过多巴胺的贻贝启发化学法使用六方氮化硼(hBN)纳米颗粒、银纳米颗粒(AgNPs)和聚多巴胺(pdopa),以获得聚多巴胺包覆的hBN(hBN@pdopa)和银纳米颗粒修饰的hBN@pdopa(hBN@pdopa-AgNPs)。对这两种纳米结构进行了研究以观察愈合阶段。
选择银纳米颗粒用于减轻炎症,六方氮化硼用于诱导细胞增殖和迁移。在体外实验中,首先评估了hBN@pdopa和hBN@pdopa-AgNPs的高细胞摄取能力和生物相容性。还测试了它们对受损细胞中活性氧(ROS)浓度升高的反应。最后,分别通过光学显微镜和共聚焦显微镜监测它们对细胞迁移、细胞内管形成和F-肌动蛋白组织的影响。
结果清楚地表明,hBN@pdopa-AgNPs显著降低活性氧的产生,促进伤口闭合,并重组细胞中的管形成。